The effects of adipose tissue-derived stem cells seeded onto the curcumin-loaded collagen scaffold in healing of experimentally induced oral mucosal ulcers in rat | ||
Iranian Journal of Basic Medical Sciences | ||
مقاله 15، دوره 23، شماره 12، اسفند 2020، صفحه 1618-1627 اصل مقاله (1.66 M) | ||
نوع مقاله: Original Article | ||
شناسه دیجیتال (DOI): 10.22038/ijbms.2020.48698.11171 | ||
نویسندگان | ||
Maryam Mardani1؛ Azita Sadeghzadeh* 2؛ Nader Tanideh3؛ Azadeh Andisheh Tadbir4؛ Fatemeh Lavaee1؛ Moein Zarei5؛ Javad Moayedi6، 7 | ||
1Oral and Dental Disease Research Center, Department of Oral and Maxillofacial Medicine, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran | ||
2Postgraduate Student, Oral and Dental Disease Research Center, Department of Oral and Maxillofacial Medicine, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran | ||
3Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran | ||
4Oral and Dental Disease Research Center, Department of Oral and Maxillofacial Pathology, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran | ||
5West Pomeranian University of Technology, Szczecin, Department of Polymer and Biomaterials Science, Al. Piastow 45, 71-311 Szczecin, Poland | ||
6Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran | ||
7Center of Comparative and Experimental Medicine, Shiraz University of Medical Sciences, Shiraz, Iran | ||
چکیده | ||
Objective(s): Various therapeutic approaches, including stem-cell-based strategies and tissue engineering, have been proposed for oral ulcerative lesions. We investigated the effects of adipose tissue-derived stem cells (ADSCs) seeded onto the curcumin-loaded collagen scaffold in the mucosal healing of oral ulcers in rats. Materials and Methods: The current experimental study was conducted on 40 male Sprague-Dawley rats. Oral ulcers were created over both sides of buccal mucosa, and the rats were randomly divided into four equal groups: 1) an untreated group (negative control); 2) Teriadent-treated group (positive control); 3) group treated with curcumin-loaded collagen scaffold; and 4) group received the ADSCs (3 × 106 cells) seeded onto the curcumin-loaded collagen scaffold. Rats were sacrificed on 3rd and 7th day after ulceration for histopathological examination as well as measurement of tissue levels of myeloperoxidase (MPO), superoxide dismutase (SOD), and Interleukin-1 beta (IL-1β) activity. Results: Compared with the negative control, the tissue levels of MPO and IL-1β were significantly decreased in all treated groups (p <0.0001); however, the SOD activity was elevated (p <0.0001). The highest SOD activity as well as the lowest MPO and IL-1β levels were observed in the ADSCs-curcumin-loaded collagen scaffold group. The ulcer healing process at 3rd and 7th day follow-up was much more progressed in the ADSCs-curcumin-loaded collagen scaffold group in comparison with the untreated group (P=0.037 and P=0.004, respectively). Conclusion: According to the findings of this study, ADSCs seeded onto the curcumin-loaded collagen scaffold seems to have a promising potential for oral ulcer healing applications. | ||
کلیدواژهها | ||
ADSCs؛ Collagen؛ Curcumin؛ Experimental؛ Oral ulcers؛ Scaffold؛ Ulcer healing | ||
مراجع | ||
1. Jinbu Y, Demitsu T. Oral ulcerations due to drug medications. Jpn Dent Sci Rev 2014; 50:40-46. 2. Leão JC, Gomes VB, Porter S. Ulcerative lesions of the mouth: an update for the general medical practitioner. Clinics 2007; 62:769-780. 3. Fourie J, Boy S. Oral mucosal ulceration-a clinician’s guide to diagnosis and treatment. S Afr Dent J 2016; 71:500-508. 4. Mortazavi H, Safi Y, Baharvand M, Rahmani S. Diagnostic features of common oral ulcerative lesions: an updated decision tree. Int J Dent 2016; 2016:1-14. 5. Hasnor Wan Ismail WN, Abdul Razak F, Haji Abdul Rahim Z. Oral microbes and its environment: A review article. Esteem Acad J 2013; 9:67-75. 6. Politis C, Schoenaers J, Jacobs R, Agbaje JO. Wound healing problems in the mouth. Front Physiol 2016; 7:1-13. 7. Suma G, Arora MP, Lakhanpal M. Stem cell therapy: A novel treatment approach for oral mucosal lesions. J Pharm Bioallied Sci 2015; 7:2-8. 8. Kinikoglu B, Damour O, Hasirci V. Tissue engineering of oral mucosa: a shared concept with skin. J Artif Organs 2015; 18:8-19. 9. Chagastelles PC, Nardi NB. Biology of stem cells: an overview. Kidney Int Suppl 2011; 1:63-67. 10. Frese L, Dijkman PE, Hoerstrup SP. Adipose tissue-derived stem cells in regenerative medicine. Transfus Med Hemother 2016; 43:268-274. 11. Khosravi Maharlooei M, Bagheri M, Solhjou Z, Moein Jahromi B, Akrami M, Rohani L, et al. Adipose tissue derived mesenchymal stem cell (AD-MSC) promotes skin wound healing in diabetic rats. Diabetes Res Clin Pract 2011; 93:228-234. 12. Mazini L, Rochette L, Amine M, Malka G. Regenerative capacity of adipose derived stem cells (ADSCs), comparison with mesenchymal stem cells (MSCs). Int J Mol Sci 2019; 20:2523-2553. 13. Theoret C. Tissue engineering in wound repair: the three “R”s-repair, replace, regenerate. Vet Surg 2009; 38:905-913. 14. Chevallay B, Herbage D. Collagen-based biomaterials as 3D scaffold for cell cultures: applications for tissue engineering and gene therapy. Med Biol Eng Comput 2000; 38:211-218. 15. Dash B, Xu Z, Lin L, Koo A, Ndon S, Berthiaume F, et al. Stem cells and engineered scaffolds for regenerative wound healing. Bioengineering 2018; 5:23-42. 16. Rahmani Del Bakhshayesh A, Annabi N, Khalilov R, Akbarzadeh A, Samiei M, Alizadeh E, et al. Recent advances on biomedical applications of scaffolds in wound healing and dermal tissue engineering. Artif Cells Nanomed Biotechnol 2018; 46:691-705. 17. Brett D. A review of collagen and collagen-based wound dressings. Wounds 2008; 20:347-356. 18. Rangaraj A, Harding K, Leaper D. Role of collagen in wound management. Wounds 2011; 7:54-63. 19. Chattopadhyay S, Raines RT. Collagen‐based biomaterials for wound healing. Biopolymers 2014; 101:821-833. 20. Karri VVSR, Kuppusamy G, Talluri SV, Mannemala SS, Kollipara R, Wadhwani AD, et al. Curcumin loaded chitosan nanoparticles impregnated into collagen-alginate scaffolds for diabetic wound healing. Int J Biol Macromol 2016; 93:1519-1529. 21. Arpita R, Ansul K, Shamimul H, Shazina S. Curcumin in oral mucosal lesions: an update. Asian J Pharm Clin Res 2019; 12:32-43. 22. Lim YS, Kwon SK, Park JH, Cho CG, Park SW, Kim WK. Enhanced mucosal healing with curcumin in animal oral ulcer model. Laryngoscope 2016; 126:68-73. 23. Zaher A, Elsabaa H, Abou Elkhier M, Elhindawy M. Impact of curcumin on tongue ulcer healing in albino rats. Mansoura J Dent 2014; 1:85-89. 24. Brahatheeswaran D, Mathew A, Aswathy RG, Nagaoka Y, Venugopal K, Yoshida Y, et al. Hybrid fluorescent curcumin loaded zein electrospun nanofibrous scaffold for biomedical applications. Biomed Mater 2012; 7:045001. 25. Wei L-G, Chang H-I, Wang Y, Hsu S-h, Dai L-G, Fu K-Y, et al. A gelatin/collagen/polycaprolactone scaffold for skin regeneration. PeerJ 2019; 7:e6358. 26. Terzi A, Storelli E, Bettini S, Sibillano T, Altamura D, Salvatore L, et al. Effects of processing on structural, mechanical and biological properties of collagen-based substrates for regenerative medicine. Sci Rep 2018; 8:1-13. 27. Taléns-Visconti R, Bonora A, Jover R, Mirabet V, Carbonell F, Castell JV, et al. Hepatogenic differentiation of human mesenchymal stem cells from adipose tissue in comparison with bone marrow mesenchymal stem cells. World J Gastroenterol 2006; 12:5834-5845. 28. Mehrabani D, Hassanshahi MA, Tamadon A, Zare S, Keshavarz S, Rahmanifar F, et al. Adipose tissue-derived mesenchymal stem cells repair germinal cells of seminiferous tubules of busulfan-induced azoospermic rats. J Hum Reprod Sci 2015; 8:103-110. 29. Karimaghai N, Tamadon A, Rahmanifar F, Mehrabani D, Raayat Jahromi A, Zare S, et al. Spermatogenesis after transplantation of adipose tissue-derived mesenchymal stem cells in busulfan-induced azoospermic hamster. Iran J Basic Med Sci 2018; 21:660-667. 30. Hashemi SS, Pourfath MR, Derakhshanfar A, Behzad-Behbahani A, Moayedi J. The role of labeled cell therapy with and without scaffold in early excision burn wounds in a rat animal model. Iran J Basic Med Sci 2020; 23:673-679. 31. de Barros Silva PG, de Codes ÉBB, Freitas MO, de Lima Martins JO, Alves APNN, Sousa FB. Experimental model of oral ulcer in mice: Comparing wound healing in three immunologically distinct animal lines. J Oral Maxillofac Pathol 2018; 22:444-451. 32. Oliveira BV, Barros Silva PG, Nojosa JDS, Brizeno LAC, Ferreira JM, Sousa FB, et al. TNF-alpha expression, evaluation of collagen, and TUNEL of Matricaria recutita L. extract and triamcinolone on oral ulcer in diabetic rats. J Appl Oral Sci 2016; 24:278-290. 33. Lima V, Brito G, Cunha F, Rebouças C, Falcão B, Augusto R, et al. Effects of the tumour necrosis factor‐α inhibitors pentoxifylline and thalidomide in short‐term experimental oral mucositis in hamsters. Eur J Oral Sci 2005; 113:210-217. 34. Khan I, Arany P. Biophysical approaches for oral wound healing: emphasis on photobiomodulation. Adv Wound Care 2015; 4:724-737. 35. Chen L, Arbieva ZH, Guo S, Marucha PT, Mustoe TA, DiPietro LA. Positional differences in the wound transcriptome of skin and oral mucosa. BMC Genomics 2010; 11:471-486. 36. Hashemipour M, Borna R, Gandjaliphan Nassab A. Effects of mucoadhessive paste of chlorhexidine and betamethasone on oral ulcer recovery process in rats. Wounds 2013; 25:104-112. 37. Franck CL, Senegaglia AC, Leite LMB, de Moura SAB, Francisco NF, Ribas Filho JM. Influence of adipose tissue-derived stem cells on the burn wound healing process. Stem Cells Int 2019; 2019:1-10. 38. Jiang Y, Chen B, Liu Y, Zhufu Z, Yan X, Hou X, et al. Effect of collagen scaffold with adipose-derived stromal vascular fraction cells on diabetic wound healing: A study in a diabetic porcine model. Tissue Eng Regen Med 2013; 10:192-199. 39. Jansen RG, van Kuppevelt TH, Daamen WF, Kuijpers-Jagtman AM, Von den Hoff JW. Tissue reactions to collagen scaffolds in the oral mucosa and skin of rats: environmental and mechanical factors. Arch Oral Biol 2008; 53:376-387. 40. Shi Y, Zhang H, Zhang X, Chen Z, Zhao D, Ma J. A comparative study of two porous sponge scaffolds prepared by collagen derived from porcine skin and fish scales as burn wound dressings in a rabbit model. Regen Biomater 2020; 7:63-70. 41. Espinosa L, Sosnik A, Fontanilla M. Development and preclinical evaluation of acellular collagen scaffolding and autologous artificial connective tissue in the regeneration of oral mucosa wounds. Tissue Eng Part A 2010; 16:1667-1679. 42. Polat NH, Kinali NA. Curcumin-loaded bio-based electrospun polyurethane scaffolds. Cumhuriyet Sci J 2019; 40:125-135. 43. Hoang MS. Fabrication of curcumin loaded nano polycaprolactone/chitosan nonwoven fabric via electrospinning technique. Vietnam J Sci Technol 2017; 55:99-108. 44. Shababdoust A, Ehsani M, Shokrollahi P, Zandi M. Fabrication of curcumin-loaded electrospun nanofiberous polyurethanes with anti-bacterial activity. Prog Biomater 2018; 7:23-33. 45. Suwantong O, Opanasopit P, Ruktanonchai U, Supaphol P. Electrospun cellulose acetate fiber mats containing curcumin and release characteristic of the herbal substance. Polymer 2007; 48:7546-7557. 46. Amirthalingam M, Kasinathan N, Amuthan A, Mutalik S, Sreenivasa Reddy M, Nayanabhirama U. Bioactive PLGA–curcumin microparticle-embedded chitosan scaffold: in vitro and in vivo evaluation. Artif Cells Nanomed Biotechnol 2017; 45:233-241. 47. Mutlu G, Calamak S, Ulubayram K, Guven E. Curcumin-loaded electrospun PHBV nanofibers as potential wound-dressing material. J Drug Deliv Sci Technol 2018; 43:185-193. 48. Rezaei A, Nasirpour A. Encapsulation of curcumin using electrospun almond gum nanofibers: fabrication and characterization. Int J Food Prop 2018; 21:1608-1618. 49. Rezai Rad M, Bohloli M, Akhavan Rahnama M, Anbarlou A, Nazeman P, Khojasteh A. Impact of tissue harvesting sites on the cellular behaviors of adipose-derived stem cells: implication for bone tissue engineering. Stem Cells Int 2017; 2017:1-9. 50. Sardaro N, Della Vella F, Incalza MA, Di Stasio D, Lucchese A, Contaldo M, et al. Oxidative stress and oral mucosal diseases: An overview. In vivo 2019; 33:289-296. 51. Kesarwala AH, Krishna MC, Mitchell JB. Oxidative stress in oral diseases. Oral Dis 2016; 22:9-18. 52. Wang Y, Branicky R, Noë A, Hekimi S. Superoxide dismutases: Dual roles in controlling ROS damage and regulating ROS signaling. J Cell Biol 2018; 217:1915-1928. 53. Queiroz-Junior CM, Pacheco CMdF, Fonseca AH, Klein A, Caliari MV, de Francischi JN. Myeloperoxidase content is a marker of systemic inflammation in a chronic condition: the example given by the periodontal disease in rats. Mediators Inflamm 2009; 2009:1-7. 54. Hasmann A, Wehrschütz-Sigl E, Marold A, Wiesbauer H, Schoeftner R, Geweßler U, et al. Analysis of myeloperoxidase activity in wound fluids as a marker of infection. Ann Clin Biochem 2013; 50:245-254. 55. Nguyen V-L, Truong C-T, Nguyen BCQ, Van Vo T-N, Dao T-T, Nguyen V-D, et al. Anti-inflammatory and wound healing activities of calophyllolide isolated from Calophyllum inophyllum Linn. PLoS One 2017; 12:e0185674. 56. Qian L, Fourcaudot A, Yamane K, You T, Chan R, Leung K. Exacerbated and prolonged inflammation impairs wound healing and increases scarring. Wound Repair Regen 2016; 24:26-34. 57. Harrell CR, Fellabaum C, Jovicic N, Djonov V, Arsenijevic N, Volarevic V. Molecular mechanisms responsible for therapeutic potential of mesenchymal stem cell-derived secretome. Cells 2019; 8:467-501. 58. Chainani-Wu N, Silverman Jr S, Reingold A, Bostrom A, Lozada-Nur F, Weintraub J. Validation of instruments to measure the symptoms and signs of oral lichen planus. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2008; 105:51-58. 59. Shen L-R, Xiao F, Yuan P, Chen Y, Gao Q-K, Parnell LD, et al. Curcumin-supplemented diets increase superoxide dismutase activity and mean lifespan in Drosophila. Age 2013; 35:1133-1142. 60. Cho J-W, Lee K-S, Kim C-W. Curcumin attenuates the expression of IL-1β, IL-6, and TNF-α as well as cyclin E in TNF-α-treated HaCaT cells; NF-κB and MAPKs as potential upstream targets. Int J Mol Med 2007; 19:469-474. 61. Yin H, Guo Q, Li X, Tang T, Li C, Wang H, et al. Curcumin suppresses IL-1β secretion and prevents inflammation through inhibition of the NLRP3 inflammasome. J Immunol 2018; 200:2835-2846. 62. Jin R, Shen M, Yu L, Wang X, Lin X. Adipose-derived stem cells suppress inflammation induced by IL-1β through down-regulation of P2X7R mediated by miR-373 in chondrocytes of osteoarthritis. Mol Cells 2017; 40:222-229. 63. He L, Zhu C, Jia J, Hao X-Y, Yu X-Y, Liu X-Y, et al. ADSC-Exos containing MALAT1 promotes wound healing by targeting miR-124 through activating Wnt/β-catenin pathway. Biosci Rep 2020; 40:1-13. 64. Li X, Xie X, Lian W, Shi R, Han S, Zhang H, et al. Exosomes from adipose-derived stem cells overexpressing Nrf2 accelerate cutaneous wound healing by promoting vascularization in a diabetic foot ulcer rat model. Exp Mol Med 2018; 50:1-14. 65. Rashed FM, GabAllah OM, AbuAli SY, Shredah MT. The effect of using bone marrow mesenchymal stem cells versus platelet-rich plasma on the healing of induced oral ulcer in albino rats. Int J Stem Cells 2019; 12:95-106. | ||
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