BMJ Open Diabetes Research & Care
BMJ Publishing Group
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Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
Volume: 8, Issue: 1
DOI 10.1136/bmjdrc-2019-001033
Abstract

ObjectiveWe assessed the therapeutic effects of photobiomodulation (PBM) and adipose-derived stem cell (ADS) treatments individually and together on the maturation step of repairing of a delayed healing wound model in rats with type 1 diabetes mellitus (DM1).Research design and methodsWe randomly assigned 24 rats with DM1 to four groups (n=6 per group). Group 1 was the control (placebo) group. In group 2, allograft human ADSs were transplanted. Group 3 was subjected to PBM (wavelength: 890 nm, peak power output: 80 W, pulse frequency: 80 Hz, pulsed duration: 180 ns, duration of exposure for each point: 200 s, power density: 0.001 W/cm2, energy density: 0.2 J/cm2) immediately after surgery, which continued for 6 days per week for 16 days. Group 4 received both the human ADS and PBM. In addition, we inflicted an ischemic, delayed healing, and infected wound simulation in all of the rats. The wounds were infected with methicillin-resistant Staphylococcus aureus (MRSA).ResultsAll three treatment regimens significantly decreased the amount of microbial flora, significantly increased wound strength and significantly modulated inflammatory response and significantly increased angiogenesis on day 16. Microbiological analysis showed that PBM+ADS was significantly better than PBM and ADS alone. In terms of wound closure rate and angiogenesis, PBM+ADS was significantly better than the PBM, ADS and control groups.ConclusionsCombination therapy of PBM+ADS is more effective that either PBM or ADS in stimulating skin injury repair, and modulating inflammatory response in an MRSA-infected wound model of rats with DM1.

Keywords
Ebrahimpour-Malekshah, Amini, Zare, Mostafavinia, Davoody, Deravi, Rahmanian, Hashemi, Habibi, Ghoreishi, Chien, Shafikhani, Ahmadi, Bayat, and Bayat: Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus
Significance of this study

What is already known about this subject?

    The positive impact of combined application of photobiomodulation (PBM) and Adipose derived stem cells (ADS) has been reported in some ischemic non diabetic tissue in animal models.

What are the new findings?

    We found that PBM and ADS alone or together significantly hasten the skin injury repair in an ischemic delayed healing and MRSA-infected wound simulation in rats with type one diabetes.
    Furthermore, combined use of PBM and ADS have confirmed a synergistic impact.

How might these results change the focus of research or clinical practice?

    Our results might support new healing attitudes for a cure and resolution of delayed healing of diabetic foot ulcer in patients.
    This approach could modulate the immune system in patients with diabetes who have delayed healing and infected diabetic foot ulcer.
    The combined application of ADS and PBM would be significant for advancing the development of a new treatment for delayed healing and infected diabetic foot ulcers in patients, and it would provide new findings about modulating the inflammatory response in diabetic foot ulcer.

Introduction

Type 1 diabetes mellitus (DM1) is a chronic illness that results from inadequate insulin production by the pancreas.1 In 2017, there were 451 million individuals worldwide who suffered from DM.2 The incidence of DM1 is estimated to increase to nearly 700 million by 2045. Approximately 50% of all persons living with DM are unidentified.2

People who suffer from DM are at greater risk for diabetic foot ulcers (DFUs). DFUs are the result of concurrent activities of many causative sources. Persistent hyperglycemia, peripheral neuropathy, ischemia from peripheral vasculopathy, immunosuppression and infection are the major pathological elements that lead to foot deformities and DFUs.3 Of note, any DFU is assumed to have blood vessel deficiencies, even without direct verification.4 In addition to metabolic aberrations, DM causes overproduction of mitochondrial superoxide and reactive oxygen species (ROS) in endothelial cells, which further leads to reduced angiogenesis and ischemia.5

Lower limb amputation (LLA) occurs in 5%–24% of patients with DFUs within 180–545 days after the initial diagnosis.6 Worldwide, DFUs are the most common complications that lead to huge financial problems for the patients, their relatives and the public.7 The total clinical cost for managing diabetic lower limb complications in the USA is approximately US$10.5 billion in addition to the cost of DM management.8

Approximately 50% of LLA occur in patients with DM, and most are from microbial DFU.9 The prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in infected DFU is 15%–30%.10 Among microbes S. aureus is the most prevalent. Overuse of antibiotics to combat infected diabetic ulcers have led to an explosion of antibiotic resistance with delayed macrophage response, which poses a serious threat to global public health.11

DFU is the main medical threat due a lack of knowledge about its pathophysiology.12 Weakened wound repair in DM is identified by reduced angiogenesis, decreased endothelial progenitor cell recruitment, reduced fibroblast and keratinocyte proliferation and migration and delayed macrophage response.12 13 The capability to quickly repair the wound is demanding and is the crucial aim for a cure for DFU.14 Both protective and curative measures consist of the use of bactericidal mediators, wet absorbent and bioengineered gauzes, vacuum-assisted closure, Regranex PDGF gel and unloading to stimulate the repair process.15 However, none of these measures show any distinct advantage over the others; the cure of chronic wounds and DFU remains problematic and prolonged.14 15 Thus, new approaches are urgently needed to combat infection and stimulate tissue repair in diabetic wounds. Concentrated efforts on the effectiveness of prognostic laboratory experiments, technologies for new cures and selective and focused approaches are required.4

Mesenchymal stem cells (MSCs) can effectively enhance repair of wound. The ability of MSCs to differentiate into various cell lines and their low immunogenicity make them highly attractive for therapeutic use in DFUs. MSCs stimulate cell migration, new blood vessel formation, re-epithelialization and new wound bed formation and maturation. In addition, they reduce the inflammatory response, enhance wound contraction, and can improve healing.16

Adipose-derived stem cells (ADSs) are great replacements of bone marrow (BM) MSCs because they can be simply harvested from adipose tissue and can grow in a culture system. Published investigational probes have indicated that ADSs could improve wound repair via boosting re-epithelialization and new wound bed formation. They modulate the inflammatory reaction, have an anti-apoptotic impact and secrete angiogenic growth factors.17

Probes using animal simulation18 and studies in humans19 have been performed to display the probable favorable impacts of ADS in wounds and ischemic organs in animals and in patients who suffer from DM. Despite the current achievements, several chief obstacles remain before they can be effectively used to benefit diabetic ADS in wound repair. First, the aberrant in vivo micro milieu of people with DM adversely affects the therapeutic biological action of the ADSs on wound repair.20 Second, the systemic deficiency of the healing potential of diabetic ADS in vivo.21 Third, ADS is physiologically damaged.22 Finally, ADSs cannot provide a blood vessel complex. Consequently, these diabetic ADS are weak in stimulating new blood vessel formation and soft tissue repair.23

Photobiomodulation (PBM) decreases pain, and inflammation, and enhances injury repair, and prevents cell and tissue damage.24 We believe that PBM could overcome these ADS deficiencies and synergize its positive effects in stimulating tissue repair. PBM has long been used as a means to increase circulation and improve tissue repair by enhancing new blood vessel formation through increases in vascular endothelial growth factor release and hypoxia-induced factor-1α expression.25 PBM has been shown to improve the angiogenic impact of ADS by increasing its viability and encouraging the release of cytokines in the cutaneous flap,26 ischemic limbs27 and injured skin.28

More than 100 recognized factors are involved in the insufficient skin injury repair observed in people with DM.29 The therapeutic use of a combination of beneficial mediators and biomodulators appears to be of benefit in non-healing wounds; they are likely to show a synergistic effect and can improve the success of a cure for different wound simulations. In recent experiments, Bayat group have reported the capability of the combination of PBM and conditioned media (CM) from human bone marrow mesenchymal stem cells (hBM-MSCs) to stimulate repair of weakened wounds in a rat model of streptozotocin (STZ)-induced DM1. The outcomes of these experiments showed that PBM+CM prompted anti-inflammatory and angiogenic actions, and accelerated skin injury repair in a DM1 simulation of an MRSA-infected skin injury.30 The combination of CM and PBM revealed a synergistic influence.31 Here, we intend to assess the impact of PBM and ADS treatments, alone and in combination, on the maturation step of a repair course of ischemic, delayed healing, and infected wound simulations in rats with DM1. The combined application of PBM and ADS could advance the repairing course and assist with healing severe cases of DFUs in people with DM.

Materials and methods

Animals and study design

We randomly assigned 24 male Wistar rats aged 3 months into four groups (n=6 per group). Group 1 was the control (placebo) group. In group 2, allograft human ADS were transplanted. Group 3 received PBM treatment. The fourth group received an allograft of human ADS and PBM treatment. DM1 was induced in all rats. In addition, an ischemic, delayed healing and infected wound simulation was inflicted on all of the rats. We performed microbiological examinations, wound closure rate, wound strength and histological and stereological tests on days 0, 4, 8, 12 and 16. We considered day 4 to be the inflammation step, day 8 to be the proliferation step and days 12 and 16 were the early and late maturation steps for the skin injury repair.

Isolation, expansion and immunophenotyping of human hypodermis ADSs

Human hypodermis adipose tissue was donated by a healthy adult donor (aged 35–40 years) who underwent cosmetic mammoplasty surgery. The patient provided informed consent for the use of her tissue. Approximately 5 cc of adipose tissue was manually minced, washed with phosphate buffered saline (PBS) supplemented with 100 U/mL penicillin+100 µg/mL streptomycin and subjected to digestion with 0.1% collagenase type I solution. Then, the cell pellets were suspended in Dulbecco’s Modified Eagle’s medium (DMEM)+20% fetal bovine serum (FBS) and then seeded in T-75 flasks with DMEM+20% FBS, and the above-mentioned antibiotics. We performed flow cytometry analysis to characterize the ADS cells for MSC markers, as reported previously.32 33

ADS transplantation

At 24 hours after surgery, we mixed 1×106 passage-4 ADS cells34 in 300 µL PBS.31 The mixture was immediately injected intradermally by an insulin syringe into eight sites around each wound at a 4–5 mm distance from the wound’s margin (figure 1).

A photo of the wound, photobiomodulation (PBM) target points, and adipose-derived stem cells (ADS) injection points.
Figure 1
A photo of the wound, photobiomodulation (PBM) target points, and adipose-derived stem cells (ADS) injection points.

Induction of DM1

DM1 was induced through injection of STZ (40 mg/kg, intraperitoneal).31 DM1 was validated as a blood sugar level higher than 250 mg/dL. All rats with diabetes were kept for 1 month to ensure that DM1 was established in the animals.31

Clinical examinations

We monitored the rats’ body weights and blood sugar levels throughout the experiment.

Surgery

The rats were anesthetized by intramuscular injections of ketamine (50 mg/kg) and xylazine (5 mg/kg). A dorsal, bipedicle skin flap (10×3.5 cm) was generated deep into the skin muscle. A 12 mm full-thickness excisional round wound that included the skin muscle was produced in the midpoint region of the flap by a biopsy punch. A donut-shaped silicone skin holder was fixed around each skin defect with a 04-silk suture (figure 1). Before surgery, all rats were treated with 20 mg/kg ibuprofen every 8–12 hours, which was continued until 5 days after surgery.

Inoculation of MRSA into the wounds and microbiological examination

We used the MRSA strain of S. aureus (ATCC 25923) according to a previously described procedure.31 In summary, a colony of MRSA was prepared for a final concentration of 2×108 at 1 cc and a 100 µL aliquot that contained 2×107 MRSA was administered topically onto each wound immediately after surgery. Microbiological samples for routine microbiological analyses were taken from the wounds on days 8 and 16. The numbers of bacterial per animal were counted as colony-forming units (CFUs).31

Photobiomodulation

Wounds from the rats in groups 3 and 4 were subjected to PBM immediately after surgery, which continued for 6 days per week for 16 days. The rats were sedated with the anesthetizing drugs (figure 1).31 Since the PBM target area (wound area and adjacent unwounded skin) was larger than laser probe beam area, we radiated nine shootings of the laser probe in each session of PBM therapy in order to cover all target area (a 33 mm×33 mm quadrangular area including wound in the center and adjacent unwounded skin around wound), and to make sure that all the PBM target area could receive almost the same energy density of the PBM. Complete information of PBM protocol is reported in table 1.

Table 1
Complete specifications for the photobiomodulation
ParametersDose and unit
Peak power output80 W
Average power0.001 W
Power density0.001 W/cm2
Wavelength890 nm
Wavelength range of the device890±10 nm
Pulse frequency80 Hz
Spot size1 cm2
Diameter1.12 cm
Pulsed duration180 ns
Duration of exposure for each point200 s
Energy density0.2 J/cm2
Number of laser shootings in each session9
Total energy densities at one session, and total sessions1.8 and 25.2 J/cm2
ProbeL07
CompanyMUSTANG 2000, Technica, Russia

Wound closure rate

We photographed the wounds on days 0, 4, 8, 12 and 16, and calculated and compared the wound closure rate in the study groups and at each time point.

Wound closure rate=((original wound area−open area on X day)/original wound area)×100%.35

Wound strength examination

We harvested one 5×50 mm standard sample from the wounds of all the euthanized rats at day 16 after they were euthanized. The samples were placed in a material testing machine. The deformation ratio was 0.166 mm/s. From the load-deformation curve, we calculated the tensiometeric properties including bending stiffness (MPa), maximum force (N), stress high load (N/cm2) and energy absorption (J) of the samples.31

Histological and stereological analyses

The sample from euthanized rats were excised, prepared for light histological study and serially sectioned into 5 µm sections. We stained 10 sections by H&E and 5 sections by Mallory’s trichrome staining methods.

Estimation of the cell numbers

The physical dissector method was used to determine the numerical density (Nv) of the neutrophils, macrophages, and fibroblasts, as follows:

Nv=Q/(h×a/f×p)

where Nv is numerical density; ΣQ is number of nuclei; h is height of the dissector; a/f is counting frame area; Σp is number of counting frames in all fields.

N (total of cells in each rat)=Nv×V

where Nv is numerical density; V is final total volume.35

Estimation of vascular length=2ΣQ/(Σp×a/f)

where 2ΣQ (total number of the vessel profiles counted per rat skin)/ΣP (number of counting frames in all fields (a/f)).36 Vascular length was considered as a biomarker for angiogenesis.

Statistical analysis

Data are shown as mean±SD. We used the t-test, one-way analysis of variance, repeated measurement analysis and the least significant difference (LSD) tests for statistical analyses. A p value of <0.05 was considered to be statistically significant.

Results

Marker expressions

Flow cytometry analysis showed that the ADS cells slightly expressed CD45 (0.8%) and CD11b (0.33%). In addition, the ADS cells completely expressed CD44H (100%) and CD105 (100%) as seen in online supplementary material.

10.1136/bmjdrc-2019-001033.supp1

bmjdrc-2019-001033supp001.pdf

Clinical observations

All p values were related to the LSD test. All of the rats developed clinical evidence of DM1 with a significant increase in blood sugar levels and a decrease in body weight after STZ injection. On day 4, rats in the PBM and PBM+ADS groups had a significant decrease in weight compared with the ADS group (LSD, p=0.006 and 0.016) and the control group (LSD, p=0.020 and 0.046), respectively. Although this downtrend continued for the PBM group until day 16, the PBM+ADS group experienced a weight gain. The combination of PBM+ADS significantly increased body weight compared with PBM alone. Complete information of body weights and glucose levels are shown in table 2, and by a graph in online supplementary material.

Table 2
Comparison of body weights and blood sugar levels in the studied groups
Groups→ControlPBMADSPBM+ADS
Factors↓
Initial blood sugar (mg/dL)445±44.96366.0±62.39332.86±72.89403.87±67.47
Final blood sugar (mg/dL)460±21.03425.3±74.85**361.6±58.50354.14±60.93
Initial body weight (g)310.4±12.6300.75±19.14301.57±12.2304.75±9.58
Final body weight (g)265.75±15.95*246.5±14.26*295.80±14.17294±16.35
*P<0.05, **p<0.01; Student’s t-test.
ADS, adipose-derived stem cell; PBM, photobiomodulation.

Microbial findings

Day 8

PBM+ADS treatment significantly decreased CFU in the wounds compared with ADS treatment (p=0.008) (figure 2).

Comparison of colony-forming units (CFUs) of methicillin-resistant Staphylococcus aureus (MRSA) wounds in the groups by the least significant difference test. **P<0.01; ***p<0.001. ADS, adipose-derived stem cell; PBM, photobiomodulation.
Figure 2
Comparison of colony-forming units (CFUs) of methicillin-resistant Staphylococcus aureus (MRSA) wounds in the groups by the least significant difference test. **P<0.01; ***p<0.001. ADS, adipose-derived stem cell; PBM, photobiomodulation.

Day 16

There were significant decreases in CFU in the PBM+ADS, PBM and ADS groups compared with the control group (all p=0.000). Treatment with PBM+ADS was significantly better than the individual PBM (p=0.006) and ADS (p=0.003) treatments (figure 2).

Wound closure rate

Day 4

There were no significant differences in the wound closure rate among the studied groups (figure 3).

Comparison of wound closure rate from all of the groups by the least significant difference test. **P<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.
Figure 3
Comparison of wound closure rate from all of the groups by the least significant difference test. **P<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.

Day 8

PBM+ADS (p=0.000), PBM (p=0.000) and ADS (p=0.001) treatments significantly increased wound closure rate compared with the control group. Treatment with PBM+ADS and PBM were significantly better than ADS treatment (both p=0.000). At the same time, PBM+ADS was significantly better than PBM treatment (p=0.000) (figure 3).

Day 12

Treatment with PBM+ADS and PBM significantly increased wound closure rate compared with the control and ADS groups (all, p=0.000) (figure 3).

Day 16

The PBM+ADS and PBM groups had significantly increased wound closure rate compared with the control and ADS groups (all, p=0.000). PBM+ADS treatment was significantly better than the individual PBM treatment (p=0.007) (figure 3).

Wound strength, bending stiffness

PBM+ADS (p=0.000), PBM (p=0.001) and ADS (p=0.003) treatments significantly increased bending stiffness compared with the control group (figure 4A).

Comparison of bending stiffness (A), maximum force (B), stress high load (C), and energy absorption (D), of the wounds in the studied groups according to the least significant difference test. *P<0.05; **p<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.
Figure 4
Comparison of bending stiffness (A), maximum force (B), stress high load (C), and energy absorption (D), of the wounds in the studied groups according to the least significant difference test. *P<0.05; **p<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.

Maximum force

PBM+ADS (p=0.000), PBM (p=0.004) and ADS (p=0.035) treatments significantly increased maximum force compared with the control group. PBM+ADS treatment was significantly better than ADS treatment (p=0.020) (figure 4B).

Stress high load

PBM+ADS (p=0.000), PBM (p=0.004) and ADS (p=0.035) treatments significantly increased stress high load compared with the control group. The PBM+ADS treatment was significantly better than the ADS treatment (p=0.020) (figure 4C).

Energy absorption

All treatments significantly increased energy absorption compared with the control group (all, p=0.000). Concurrently, ADS treatment was significantly better than treatment with PBM+ADS and PBM (both, p=0.000) (figure 4D).

Stereological findings

In the cases of inflammatory cells (neutrophils and macrophages), all treatments regimes significantly decreased neutrophils and macrophages counts individually and totally (figure 5, panels A, B and C, all p=0.000). For neutrophil count, the results of PBM+ADS and PBM were better than ADS (p=0.001, p=0.01). For macrophage count, the results of PBM+ADS and PBM were better than ADS (p=0.017, p=0.032). For inflammatory cells count, the results of PBM+ADS and PBM were better than ADS (p=0.003, p=0.01). For fibroblast number, PBM+ADS significantly increased fibroblast number compared with PBM, control and ADS groups (p=0.000, p=0.012, p=0.027) (figure 5, panel D). ADS significantly increased fibroblast number compared with PBM (p=0.04). All treatments regimes significantly increased vascular length compared with control group. In case of angiogenesis, we observed significantly more vascular length in PBM+ADS compared with ADS and PBM (p=0.007, p=0.029) (figure 5, panel E).

Comparison of number of neutrophil (A), macrophage (B), inflammatory cells (C), fibroblast (D) and vascular length (E) of wounds of four studied groups by LSD tests. *P<0.05; **p<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.
Figure 5
Comparison of number of neutrophil (A), macrophage (B), inflammatory cells (C), fibroblast (D) and vascular length (E) of wounds of four studied groups by LSD tests. *P<0.05; **p<0.01; ***p<0.001. ADS, adipose-derived stem cells; PBM, photobiomodulation.

Histological micrographs of four studied groups which were stained with H&E staining method are shown in online supplementary materials.

Findings of Mallory's trichrome staining

Photos of Mallory’s trichrome staining are shown in online supplementary materials. Collagen fibers orientation in control group were mixed, while in treatment groups were mostly horizontal. Pattern of collagen fibers in control group were mostly reticular and thin, whereas in treatment groups they were mostly fascicular and they seem thicker than collagen fibers of the control group.

Discussion

In the current study, we evaluated the impact of PBM and ADS administration alone and together on the maturation step of the repair process in an ischemic, delayed healing and infected wound simulation in rats with DM1.

The complications in treatment of DFUs include an aberrant regional milieu, excessive inflammation and angiogenesis maladies.37 The results from this study indicated that all three treatment regimens significantly modulated inflammatory response, and significantly increased angiogenesis on day 16.

A previous study from one of the authors of the current study have shown that because of ADSs immunomodulatory impressions, they might be considered an appropriate treatment of some inflammatory diseases in healthy individuals and patients with DM.38 The most recent tissue engineering methods in stem cell therapy have shown encouraging choices to repair the weakened, injured skin, including DFUs. Stem cell therapy has arisen as a unique healing method for many illnesses, comprising injury repair and tissue restoration. Many diverse stem cell types have been considered in both animal and human studies and included BM-MSCs and ADS cells for wound repair. Fat tissue provides a plentiful source for MSCs and has shown promising results in wound repair experiments. ADS cells have the capability to change into different cell lines and release paracrine factors that start the tissue restoration process. The plentiful source of adipose tissue, simplicity of extraction, huge proliferative abilities in vitro and their capacity to release pro-angiogenic cytokines make them a perfect cell type as treatment for chronic wounds and wounds.39 In addition, ADS cells can be very valuable for medical use as they prevent immunological reactions and do not require a chief histocompatibility equivalent for allogeneic engraftment.40 Engraftment of ADSs encourages new blood vessel formation and increases blood flow to the ischemic organ in mice.41 It has also been revealed that growth factors released by ADS cells stimulate arteriogenesis in ischemic tissue by paracrine signaling.41 42

To our knowledge, the combination of PBM+ADS on the repair of infected wounds in patients or animals with DM1 has not been documented. This study aimed to assess the impacts of PBM+ADS on microbial flora, wound area, wound strength and histological parameters in rats with DM1. We found that the use of PBM or ADS alone, or together significantly increased skin injury repair of the MRSA-infected wounds in rats with DM1. Additionally, PBM+ADS showed a synergistic impact. Therefore, PBM+ADS treatment was significantly better than individual treatment by PBM or ADS. This was probably the result of the enhanced survival of ADSs by inhibition of apoptosis, along with increased paracrine signaling of ADS under the influence of PBM.27 28

Our data demonstrated that an anti-inflammatory agent as well as a mitogenic agent, PBM, displayed a synergistic impression on ADS-prompted skin injury repair in rats (figure 5). The wound closure rate was increased in the group that received PBM+ADS. Interestingly, the initiation of bactericidal impact by ADSs was specially improved by PBM, companioned by the elevated wound strength. These outcomes suggested that administration of PBM at the right protocol might assist with the healing effects of ADS in a DM1 simulation of an MRSA-infected ischemic delayed healing wound. Taken together, our findings recommend that PBM, an anti-inflammatory and mitogen agent, along with a cost-effective modality could be a beneficial enhancement for ADS-based therapy in treating DFUs.

Guo and DiPietro in their review article emphasized on important of wound strength in different medical situations.43 Our study showed that treatment of wounds with ADS significantly increased wound strength compared with control and PBM groups. This result showed importance of ADS in treating non healing wounds such as diabetic wounds. However, combined administration of ADS and PBM demonstrated a synergistic effect. In current study, the results of fibroblast count and Mallory’s trichrome stain were in the line of wound strength results.

In the current study, stereological analysis supported our hypothesis that the treatments, particularly PBM+ADS modulated the inflammatory response, simultaneously increased wound strength and wound closure rate, and significantly decreased the CFU.

It should also be noted that our unique outcomes reveal the synergistic impact of PBM+ADS on skin injury repair in comparison with other related experiments that only investigated the impression of a solo cure with either PBM44 or ADS.18

Bacterial contamination is a main contributing issue in the deterioration of wound healing.45 MRSA is a common staphylococcal strain accountable for numerous regional and general contaminations that quickly progresses to resistance to regularly recommended antibiotics. Therefore, the observed occurrence and adaptation of MRSA in DFUs9 has stemmed from a growing range of non-curable staphylococcal contaminations.46 Novel approaches to treat MRSA contamination and counter the growing complication of MRSA are mandatory.34 Specifically, our experiment aimed to focus on the bactericidal effects of PBM47 and ADS34 because both have been individually reported to have bactericidal effects in animal models. To date, there is no probe that has examined the effects of PBM on immunomodulation of ADS.

Our outcomes (figure 2) show that PBM treatment could further promote the immunomodulatory efficacy of ADS and might be medically applicable to cell therapies, while better healing impact are required as DFUs, or scalds. In a study of a culture system probe with PBM (415 nm, 100 mW and 30, 60, 120 J/cm2), Lipoveski et al presented an inhibitory impact on S. aureus growth by stimulation of ROS synthesis.48 Consistent with this finding, we hypothesized that the bactericidal effect of the PBM-treated groups in this probe might be due to the induction of ROS by PBM.

Several studies have suggested that stem cells, specifically ADS cells, can speed up repair of a wound, and ADS cells can employ many actions to stimulate skin injury repair. In theory, ADS cells might immediately contribute to tissue restoration by renewing impaired cells via epidermal differentiation,49 although the weak efficiency of ADS transplantation and viability at the injury site has restricted this direct involvement.20–23 Recent investigations have shown significant decreases in stem cells quantity in some experimental simulations of fractures and wounds within the first 14 days of engraftment. Wu et al reported a considerable increase in stem cell survival 7 days after creating the skin injury and a fast decrease in surviving cells 14 days after the infliction of this skin injury.50 Levi et al studied the effect of human ADS implantation on the repair of a non-healing mice skull defect. They observed significant repair in the implanted skull defect. In their study, at 28 and 56 days after the human ADS implantation, many of the fluorescence in situ hybridization positive cells were not recognized.51 The outcomes from two probes demonstrated that some implanted ADS cells expressed endothelial markers and were absorbed into vascular networks in ischemic organs, but the rate of contribution was small because many cells expired inside the hypoxic milieu of the ischemic organ.52 Hence, to improve positive stem cell therapies, it is essential to improve stem cell function, so they can stay alive in ischemic tissue and be able to differentiate into vascular cells, as well.53

PBM has been successfully applied for enhancement of local blood circulation and improve repair of an injury by triggering new blood vessel formation in some non-diabetic animal simulations of ischemic tissues.25 Park et al reported that the release of cytokines was greater in the ADS+PBM group compared with the ADS-only group in a random skin flap (RSF) in mice. ADS improved tissue repair by endothelial cell differentiation and release of angiogenic growth factors. The ADS+PBM group showed better treatment efficiency in comparison with ADS alone. Park et al found that transplanting ADSs to ischemic RSF enhanced healing efficiency for ischemia as an outcome of improved ADS viability and paracrine impact. Moreover, Park et al concluded that PBM improved the viability of ADS and encouraged the release of growth factors in RSF.27

The impacts of PBM+CM of hBM-MSC on the infected wounds in rats with diabetes were studied by Bayat group. In the first study, Kouhkheil et al reported the positive impacts of PBM (890 nm, 80 Hz, 0.2 J/cm2) and CM from hBM-MSCs (four injections) together and alone on the CFU and wound strength of an infected wound simulation with MRSA in rats with DM1.31 In the second study, Fridoni et al demonstrated the positive impact of PBM (890 nm, 80 Hz, 0.2 J/cm2) and CM from hBM-MSC (four injections) alone or together on the stereological parameters of an infected wound simulation with MRSA in rats with DM1. Fridoni et al determined that the use of PBM+CM prompted anti-inflammatory and neovascular actions, and hastened skin injury repair in an MRSA-infected injury in rats with DM1.30

In current study, stereological analysis supports our hypothesis regarding our treatments and especially PBM+ADS modulates inflammatory response and at the same time increases wound strength, and significantly increased wound closure rate and CFU. Bayat and Chien have reported the positive effects of combined application of ADS and PBM in some ischemic tissues. They stressed that these results might support new healing attitudes for a cure and resolution of delayed healing of DFU in patients.54

Conclusion

PBM and ADS alone or together significantly hasten the skin injury repair in an ischemic delayed healing and MRSA-infected wound simulation in rats with DM1. Furthermore, combined use of PBM and ADS have confirmed a synergistic impact. We suggest that PBM+ADS treatment should be used for infected skin injuries and wounds in translational studies, and in patients to reduce inflammation, and infection, and promote repair. Additional details of cellular and molecular mechanisms regarding the effect of PBM+ADS on the repair of ischemic delayed healing and MRSA-infected wounds in rats with DM1 should be elucidated by further research.

Notes

Contributors:: MB is the guarantor of this work, and researched data and wrote the manuscript. SC, AA, and SMH contributed to the conception and design. RE-M, FZ, AM, SD, ND, MR, MH, and HA performed the experiments and collection of data and SB primary edited the manuscript. SKG contributed to the data analysis and interpretation. SC and SS edited scientifically the manuscript.
Funding:: This study was financially supported by the Research Department of the School of Medicine at Shahid Beheshti University of Medical Sciences (grant no. 14601). SC was supported in part by NIH grant DK105692.
Competing interests:: None declared.
Patient consent for publication:: Not required.
Ethics approval:: The IACUC of the School of Medicine at Shahid Beheshti University of Medical Sciences (SBMU) approved this experiment (file no: IR.SBMU.MSP.REC.1398.394).
Provenance and peer review:: Not commissioned; externally peer reviewed.
Data availability statement:: Data are available upon reasonable request.

References

1 

American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care2004;27 Suppl 1:, pp.S5–10., doi: 10.2337/diacare.27.2007.s5

2 

Cho NH, Shaw JE, Karuranga S, et al. IDF diabetes atlas: global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Res Clin Pract2018;138:, pp.271–81., doi: 10.1016/j.diabres.2018.02.023

3 

Clayton W, Elasy TA. A review of the pathophysiology, classification, and treatment of foot ulcers in diabetic patients. Clinical Diabetes2009;27:, pp.52–8., doi: 10.2337/diaclin.27.2.52

4 

Lepäntalo M, Apelqvist J, Setacci C, et al. Chapter V: diabetic foot. Eur J Vasc Endovasc Surg2011;42 Suppl 2:, pp.S60–74., doi: 10.1016/S1078-5884(11)60012-9

5 

Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circ Res2010;107:, pp.1058–70., doi: 10.1161/CIRCRESAHA.110.223545

6 

Alexiadou K, Doupis J. Management of diabetic foot ulcers. Diabetes Therapy2012;3:, pp.4, doi: 10.1007/s13300-012-0004-9

7 

Raghav A, Khan ZA, Labala RK, et al. Financial burden of diabetic foot ulcers to world: a progressive topic to discuss always. Ther Adv Endocrinol Metab2018;9:, pp.29–31., doi: 10.1177/2042018817744513

8 

Rice JB, Desai U, Cummings AKG, et al. Burden of diabetic foot ulcers for Medicare and private insurers. Diabetes Care2014;37:, pp.651–8., doi: 10.2337/dc13-2176

9 

Boulton AJ, Armstrong DG, Kirsner RS, et al. Diagnosis and management of diabetic foot complications, 2018 Available: https://www.ncbi.nlm.nih.gov

10 

Eleftheriadou I, Tentolouris N, Argiana V, et al. Methicillin-Resistant Staphylococcus aureus in diabetic foot infections. Drugs2010;70:, pp.1785–97., doi: 10.2165/11538070-000000000-00000

11 

Lipsky BA. Diabetic foot infections: Current treatment and delaying the ‘post-antibiotic era’. Diabetes Metab Res Rev2016;32:, pp.246–53., doi: 10.1002/dmrr.2739

12 

Catrina S-B, Zheng X. Disturbed hypoxic responses as a pathogenic mechanism of diabetic foot ulcers. Diabetes Metab Res Rev2016;32:, pp.179–85., doi: 10.1002/dmrr.2742

13 

Wood S, Jayaraman V, Huelsmann EJ, et al. Pro-Inflammatory chemokine CCL2 (MCP-1) promotes healing in diabetic wounds by restoring the macrophage response. PLoS One2014;9:e91574, doi: 10.1371/journal.pone.0091574

14 

Landén NX, Li D, Ståhle M. Transition from inflammation to proliferation: a critical step during wound healing. Cell Mol Life Sci2016;73:, pp.3861–85., doi: 10.1007/s00018-016-2268-0

15 

Powers JG, Higham C, Broussard K, et al. Wound healing and treating wounds: chronic wound care and management. J Am Acad Dermatol2016;74:, pp.607–25., doi: 10.1016/j.jaad.2015.08.070

16 

Hu MS, Borrelli MR, Lorenz HP, et al. Mesenchymal stromal cells and cutaneous wound healing: a comprehensive review of the background, role, and therapeutic potential. Stem Cells Int2018;2018:6901983, doi: 10.1155/2018/6901983

17 

Gadelkarim M, Abushouk AI, Ghanem E, et al. Adipose-Derived stem cells: effectiveness and advances in delivery in diabetic wound healing. Biomed Pharmacother2018;107:, pp.625–33., doi: 10.1016/j.biopha.2018.08.013

18 

Irons RF, Cahill KW, Rattigan DA, et al. Acceleration of diabetic wound healing with adipose-derived stem cells, endothelial-differentiated stem cells, and topical conditioned medium therapy in a swine model. J Vasc Surg. In Press2018;68:, pp.115S–25., doi: 10.1016/j.jvs.2018.01.065

19 

Lopes L, Setia O, Aurshina A, et al. Stem cell therapy for diabetic foot ulcers: a review of preclinical and clinical research. Stem Cell Res Ther2018;9:, pp.188, doi: 10.1186/s13287-018-0938-6

20 

Yao YZ, Deng CL, Wang B. [Advances in the research of influence of diabetes in biological function of adipose-derived stem cells]. Zhonghua Shao Shang Za Zhi2018;34:, pp.653–6., doi: 10.3760/cma.j.issn.1009-2587.2018.09.017

21 

Kim SM, Kim YH, Jun YJ, et al. The effect of diabetes on the wound healing potential of adipose-tissue derived stem cells. Int Wound J2016;13:, pp.33–41., doi: 10.1111/iwj.12540

22 

Cronk SM, Kelly-Goss MR, Ray HC, et al. Adipose-Derived stem cells from diabetic mice show impaired vascular stabilization in a murine model of diabetic retinopathy. Stem Cells Transl Med2015;4:, pp.459–67., doi: 10.5966/sctm.2014-0108

23 

Rennert RC, Sorkin M, Januszyk M, et al. Diabetes impairs the angiogenic potential of adipose-derived stem cells by selectively depleting cellular subpopulations. Stem Cell Res Ther2014;5:, pp.79, doi: 10.1186/scrt468

24 

Farivar S, Malekshahabi T, Shiari R. Biological effects of low level laser therapy. J Lasers Med Sci2014;5:, pp.58–62.

25 

Cury V, Moretti AIS, Assis L, et al. Low level laser therapy increases angiogenesis in a model of ischemic skin flap in rats mediated by VEGF, HIF-1α and MMP-2. Journal of Photochemistry and Photobiology B: Biology2013;125:, pp.164–70., doi: 10.1016/j.jphotobiol.2013.06.004

26 

Park I-S, Mondal A, Chung P-S, et al. Vascular regeneration effect of adipose-derived stem cells with light-emitting diode phototherapy in ischemic tissue. Lasers Med Sci2015;30:, pp.533–41., doi: 10.1007/s10103-014-1699-9

27 

Park I-S, Mondal A, Chung P-S, et al. Prevention of skin flap necrosis by use of adipose-derived stromal cells with light-emitting diode phototherapy. Cytotherapy2015;17:, pp.283–92., doi: 10.1016/j.jcyt.2014.10.017

28 

Kim H, Choi K, Kweon O-K, et al. Enhanced wound healing effect of canine adipose-derived mesenchymal stem cells with low-level laser therapy in athymic mice. J Dermatol Sci2012;68:, pp.149–56., doi: 10.1016/j.jdermsci.2012.09.013

29 

Brem H, Tomic-Canic M. Cellular and molecular basis of wound healing in diabetes. J Clin Invest2007;117:, pp.1219–22., doi: 10.1172/JCI32169

30 

Fridoni M, Kouhkheil R, Abdollhifar Mohammad‐Amin, et al. Improvement in infected wound healing in type 1 diabetic rat by the synergistic effect of photobiomodulation therapy and conditioned medium. J Cell Biochem2019;120:, pp.9906–16., doi: 10.1002/jcb.28273

31 

Kouhkheil R, Fridoni M, Piryaei A, et al. The effect of combined pulsed wave low-level laser therapy and mesenchymal stem cell-conditioned medium on the healing of an infected wound with methicillin-resistant Staphylococcal aureus in diabetic rats. J Cell Biochem2018;119:, pp.5788–97., doi: 10.1002/jcb.26759

32 

Zhu Y, Liu T, Song K, et al. Adipose-Derived stem cell: a better stem cell than BMSC. Cell Biochem Funct2008;26:, pp.664–75., doi: 10.1002/cbf.1488

33 

Muhammad G, Xu J, Bulte JWM, et al. Transplanted adipose-derived stem cells can be short-lived yet accelerate healing of acid-burn skin wounds: a multimodal imaging study. Sci Rep2017;7:4644, doi: 10.1038/s41598-017-04484-0

34 

Mot YY, Othman I, Sharifah SH. Synergistic antibacterial effect of co-administering adipose-derived mesenchymal stromal cells and Ophiophagus hannah L-amino acid oxidase in a mouse model of methicillin-resistant Staphylococcus aureus-infected wounds. Stem Cell Res Ther2017;8:, pp.5, doi: 10.1186/s13287-016-0457-2

35 

Yuan Z, Zhao J, Chen Y, et al. Regulating inflammation using acid-responsive electrospun fibrous scaffolds for skin scarless healing. Mediators Inflamm2014;2014:, pp.1–11., doi: 10.1155/2014/858045

36 

Babaei S, Bayat M, Nouruzian M, et al. Pentoxifylline improves cutaneous wound healing in streptozotocin-induced diabetic rats. Eur J Pharmacol2013;700:, pp.165–72., doi: 10.1016/j.ejphar.2012.11.024

37 

Lu H, Wu X, Wang Z, et al. Erythropoietin-activated mesenchymal stem cells promote healing ulcers by improving microenvironment. J Surg Res2016;205:, pp.464–73., doi: 10.1016/j.jss.2016.06.086

38 

Rahavi H, Hashemi SM, Soleimani M, et al. Adipose tissue-derived mesenchymal stem cells exert in vitro immunomodulatory and beta cell protective functions in streptozotocin-induced diabetic mice model. J Diabetes Res2015;2015:, pp.1–10., doi: 10.1155/2015/878535

39 

Hassan WU, Greiser U, Wang W. Role of adipose-derived stem cells in wound healing. Wound Repair Regen2014;22:, pp.313–25., doi: 10.1111/wrr.12173

40 

González MA, Gonzalez–Rey E, Rico L, et al. Adipose-Derived mesenchymal stem cells alleviate experimental colitis by inhibiting inflammatory and autoimmune responses. Gastroenterology2009;136:, pp.978–89., doi: 10.1053/j.gastro.2008.11.041

41 

Harada Y, Yamamoto Y, Tsujimoto S, et al. Transplantation of freshly isolated adipose tissue-derived regenerative cells enhances angiogenesis in a murine model of hind limb ischemia. Biomed Res2013;34:, pp.23–9., doi: 10.2220/biomedres.34.23

42 

Sumi M, Sata M, Toya N, et al. Transplantation of adipose stromal cells, but not mature adipocytes, augments ischemia-induced angiogenesis. Life Sci2007;80:, pp.559–65., doi: 10.1016/j.lfs.2006.10.020

43 

Guo S, DiPietro LA. Factors affecting wound healing. J Dent Res2010;89:, pp.219–29., doi: 10.1177/0022034509359125

44 

Sharifian Z, Bayat M, Alidoust M, et al. Histological and gene expression analysis of the effects of pulsed low-level laser therapy on wound healing of streptozotocin-induced diabetic rats. Lasers Med Sci2014;29:, pp.1227–35., doi: 10.1007/s10103-013-1500-5

45 

Edwards R, Harding KG. Bacteria and wound healing. Curr Opin Infect Dis2004;17:, pp.91–6., doi: 10.1097/00001432-200404000-00004

46 

Smith TL, Pearson ML, Wilcox KR, et al. Emergence of Vancomycin Resistance in Staphylococcus aureus. N Engl J Med Overseas Ed1999;340:, pp.493–501., doi: 10.1056/NEJM199902183400701

47 

Ranjbar R, Takhtfooladi MA. The effects of low level laser therapy on Staphylococcus aureus infected third-degree burns in diabetic rats. Acta Cirurgica Brasileira2016;31:, pp.250–5., doi: 10.1590/S0102-865020160040000005

48 

Lipovsky A, Nitzan Y, Gedanken A, et al. Visible light-induced killing of bacteria as a function of wavelength: implication for wound healing. Lasers Surg Med2010;42:, pp.467–72., doi: 10.1002/lsm.20948

49 

Li P, Guo X. A review: therapeutic potential of adipose-derived stem cells in cutaneous wound healing and regeneration. Stem Cell Res Ther2018;9:, pp.302, doi: 10.1186/s13287-018-1044-5

50 

Wu Y, Chen L, Scott PG, et al. Mesenchymal stem cells enhance wound healing through differentiation and angiogenesis. Stem Cells2007;25:, pp.2648–59., doi: 10.1634/stemcells.2007-0226

51 

Levi B, James AW, Nelson ER, et al. Human adipose derived stromal cells heal critical size mouse calvarial defects. PLoS One2010;5:e11177, doi: 10.1371/journal.pone.0011177

52 

Nakagami H, Maeda K, Morishita R, et al. Novel autologous cell therapy in ischemic limb disease through growth factor secretion by cultured adipose tissue–derived stromal cells. Arterioscler Thromb Vasc Biol2005;25:, pp.2542–7., doi: 10.1161/01.ATV.0000190701.92007.6d

53 

Bhang SH, Cho S-W, La W-G, et al. Angiogenesis in ischemic tissue produced by spheroid grafting of human adipose-derived stromal cells. Biomaterials2011;32:, pp.2734–47., doi: 10.1016/j.biomaterials.2010.12.035

54 

Bayat M, Chien S. Combined adipose-derived mesenchymal stem cells and Photobiomodulation could modulate the inflammatory response and treat infected diabetic foot ulcers. Photobiomodulation, Photomedicine, and Laser Surgery2019, doi: 10.1089/photob.2019.4670

https://www.researchpad.co/tools/openurl?pubtype=article&doi=10.1136/bmjdrc-2019-001033&title=Combined therapy of photobiomodulation and adipose-derived stem cells synergistically improve healing in an ischemic, infected and delayed healing wound model in rats with type 1 diabetes mellitus&author=Roohollah Ebrahimpour-Malekshah,Abdollah Amini,Fatemeh Zare,Atarodsadat Mostafavinia,Samin Davoody,Niloofar Deravi,Mohammad Rahmanian,Seyed Mahmoud Hashemi,Malihe Habibi,Seyed Kamran Ghoreishi,Sufan Chien,Sasha Shafikhani,Houssein Ahmadi,Sahar Bayat,Mohammad Bayat,&keyword=wound healing,&subject=Clinical Care/Education/Nutrition,1506,1866,