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Volume 13, Issue 4 (9-2026)                   jbrms 2026, 13(4): 29-38 | Back to browse issues page

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Nobakht M, Hashemi P, Kazemzadeh S, Safarkhani K, Babakhani A. Effects of Hair Follicle Stem Cells and Simvastatin on Deep Partial Thickness Wound Healing: Histological and Molecular Assay. jbrms 2026; 13 (4) :29-38
URL: http://jbrms.medilam.ac.ir/article-1-1078-en.html
Department of Anatomy, Faculty of Medicine, Ilam University of Medical Sciences, Ilam Iran , azarbabakhani58@gmail.com
Abstract:   (20 Views)
Introduction: Restoration of burn wounds in a shorter time with fewer side effects is one of the main concerns of wound management. In this study, the effects of simultaneous use of hair follicle stem cells (HFSCs) and simvastatin (SMV) in partial-thickness burn wound healing and C-X-C motif chemokine ligand 12 (CXCL12) / C-X-C chemokine receptor type 4 (CXCR4) and vascular endothelial growth factor (VEGF) expression are investigated.
Materials & Methods: Animals (male Wistar rats) were categorized into five groups: 1) control (non-treated), 2) vehicle, 3) cell (HFSCs), 4) drug (SMV), and 5) cell-drug (HFSCs + SMV). The bulge of rat whisker was isolated and cultured in DMEM/F12 and transplanted to the burn-wound site. Daily dressing was performed with petrolatum gel containing 5 μM simvastatin. At the end of therapeutic intervention, histological assessment (H&E), molecular assay (p-value blot), and tensile strength assay were performed. Statistical analyses were performed using GraphPad Prism version 6.01 (two-way repeated-measures ANOVA, one-way ANOVA, and Tukey’s post-hoc test). A p-value was considered statistically significant. Quantitative analysis of wound healing parameters was performed using ImageJ 1.46r software.
Results:  The diameter of epidermis, dermis structural integrity, and expression of SDF-1/CXCR4 and VEGF in cell-drug groups were significantly improved compared with other groups (P < 0.05). No significant differences were observed between the vehicle and control groups.
Conclusion:  Hair follicle stem cell transplantation simultaneously with simvastatin treatment accelerates the healing of the burn wounds and skin tensile strength by elevating the SDF-1 and VEGF expression levels in the injected region
Full-Text [PDF 612 kb]   (17 Downloads)    
Type of Study: Research | Subject: Cellular and molecular biology
Received: 2026/05/17 | Accepted: 2026/08/9 | Published: 2026/09/28

References
1. Ramhormozi P, Ansari JM, Simorgh S, Asgari HR, Najafi M, Barati M, et al. Simvastatin accelerates the healing process of burn wound in Wistar rats through Akt/mTOR signaling pathway. 2021;236:151652. [DOI:10.1016/j.aanat.2020.151652]
2. Ullah S, Mansoor S, Ayub A, Ejaz M, Zafar H, Feroz F, et al. An update on stem cells applications in burn wound healing. Tissue and Cell. 2021; 72:101527. [DOI:10.1016/j.tice.2021.101527]
3. Ansari JM, Ramhormozi P, Shabani R, Pazoki-Toroudi H, Yari A, Barati M, et al. Simvastatin combined with bone marrow mesenchymal stromal cells (BMSCs) improve burn wound healing by ameliorating angiogenesis through SDF-1α/CXCR4 pathway. 2020;23(6):751. [DOI:10.22038/ijbms.2020.39782.9465]
4. Lukomskyj AO, Rao N, Yan L, Pye JS, Li H, Wang B, et al. Stem cell-based tissue engineering for the treatment of burn wounds: a systematic review of preclinical studies. 2022;18(6):1926-55. [DOI:10.1007/s12015-022-10341-z]
5. Babakhani A, Nobakht M, Torodi HP, Dahmardehei M, Hashemi P, Ansari JM, et al. Effects of hair follicle stem cells on partial-thickness burn wound healing and tensile strength. 2020;24(2):99. [DOI:10.29252/ibj.24.2.99]
6. Heidari F, Yari A, Rasoolijazi H, Soleimani M, Dehpoor A, Sajedi N, et al. Bulge Hair Follicle Stem Cells Accelerate Cutaneous Wound Healing in Rats. Wounds : a compendium of clinical research and practice. 2016;28(4):132-41. [DOI:10.12968/jowc.2020.29.9.526]
7. Shao H, Tan Y, Eton D, Yang Z, Uberti MG, Li S, et al. Statin and stromal cell-derived factor-1 additively promote angiogenesis by enhancement of progenitor cells incorporation into new vessels. 2008;26(5):1376-84. [DOI:10.1634/stemcells.2007-0785]
8. Chen H, Li G, Liu Y, Ji S, Li Y, Xiang J, et al. Pleiotropic roles of CXCR4 in wound repair and regeneration. 2021;12:668758. [DOI:10.3389/fimmu.2021.668758]
9. Yari A, Heidari F, Veijouye SJ, Nobakht MJJoWC. Hair follicle stem cells promote cutaneous wound healing through the SDF-1α/CXCR4 axis: an animal model. 2020;29(9):526-36. [DOI:10.12968/jowc.2020.29.9.526]
10. John ME, Cockcroft JR, McKeever TM, Coward WR, Shale DJ, Johnson SR, et al. Cardiovascular and inflammatory effects of simvastatin therapy in patients with COPD: a randomized controlled trial. International journal of chronic obstructive pulmonary disease. 2015;10:211-21. [DOI:10.2147/COPD.S76061]
11. Matsuno H, Takei M, Hayashi H, Nakajima K, Ishisaki A, Kozawa OJJocp. Simvastatin enhances the regeneration of endothelial cells via VEGF secretion in injured arteries. 2004;43(3):333-40. [DOI:10.1097/00005344-200403000-00002]
12. Heidari F, Yari A, Teimourian S, Joulai Veijouye S, Nobakht M. Effects of Hair Follicle Stem Cells Coupled With Polycaprolactone Scaffold on Cutaneous Wound Healing in Diabetic Male Rats. The Journal of surgical research. 2023;281:200-13. [DOI:10.1016/j.jss.2022.08.008]
13. Babakhani A, Hashemi P, Mohajer Ansari J, Ramhormozi P, Nobakht M. In vitro Differentiation of Hair Follicle Stem Cell into Keratinocyte by Simvastatin. Iranian biomedical journal. 2019;23(6):404-11. [DOI:10.29252/ibj.23.6.404]
14. Amoh Y, Li L, Yang M, Moossa A, Katsuoka K, Penman S, et al. Nascent blood vessels in the skin arise from nestin-expressing hair-follicle cells. 2004;101(36):13291-5. [DOI:10.1073/pnas.0405250101]
15. Baek KH, Lee WY, Oh KW, Tae HJ, Lee JM, Lee EJ, et al. The effect of simvastatin on the proliferation and differentiation of human bone marrow stromal cells. 2005;20(3):438-44. [DOI:10.3346/jkms.2005.20.3.438]
16. Santos M, Paramio JM, Bravo A, Ramirez A, Jorcano JLJJobc. The expression of keratin k10 in the basal layer of the epidermis inhibits cell proliferation and prevents skin tumorigenesis. 2002;277(21):19122-30. [DOI:10.1074/jbc.M201001200]
17. Veith AP, Henderson K, Spencer A, Sligar AD, Baker ABJAddr. Therapeutic strategies for enhancing angiogenesis in wound healing. 2019;146:97-125.
18. Othman N, Kendrick DJBph. Epidemiology of burn injuries in the East Mediterranean Region: a systematic review. 2010;10:1-10. [DOI:10.1016/j.addr.2018.09.010]
19. Zhong S, Zhang Y, Lim CJWIRN, Nanobiotechnology. Tissue scaffolds for skin wound healing and dermal reconstruction. 2010;2(5):510-25. [DOI:10.1002/wnan.100]
20. Geesala R, Bar N, Dhoke NR, Basak P, Das AJB. Porous polymer scaffold for on-site delivery of stem cells–protects from oxidative stress and potentiates wound tissue repair. 2016;77:1-13. [DOI:10.1016/j.biomaterials.2015.11.003]
21. Planat-Benard V, Silvestre J-S, Cousin B, André M, Nibbelink M, Tamarat R, et al. Plasticity of human adipose lineage cells toward endothelial cells: physiological and therapeutic perspectives. 2004;109(5):656-63. [DOI:10.1161/01.CIR.0000114522.38265.61]
22. Tumbar T, Guasch G, Greco V, Blanpain C, Lowry WE, Rendl M, et al. Defining the epithelial stem cell niche in skin. 2004;303(5656):359-63. [DOI:10.1016/B978-0-12-802734-9.00009-3]
23. Amoh Y, Katsuoka K, Hoffman RMJJods. The advantages of hair follicle pluripotent stem cells over embryonic stem cells and induced pluripotent stem cells for regenerative medicine. 2010;60(3):131-7. [DOI:10.1016/j.jdermsci.2010.09.007]
24. Yamauchi A, Hadjur C, Takahashi T, Suzuki I, Hirose K, Mahe YFJED. Human skin melanocyte migration towards stromal cell‐derived factor‐1α demonstrated by optical real‐time cell mobility assay: modulation of their chemotactic ability by α‐melanocyte‐stimulating hormone. 2013;22(10):664-7. [DOI:10.1111/exd.12232.]

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