Low Degree Hyaluronic Acid Crosslinking Inducing the Release of TGF-Β1 in Conditioned Medium of Wharton’s Jelly-Derived Stem Cells

Authors

  • Nora Ariyati Doctoral Program, Universitas Brawijaya, Malang, Indonesia
  • Kusworini Kusworini Department of Clinical Pathology, Universitas Brawijaya, Malang, Indonesia
  • Nurdiana Nurdiana Department of Pharmacology, Universitas Brawijaya, Malang, Indonesia
  • Yohanes Widodo Wirohadidjojo Department of Dermatology and Venereology, Universitas Gadjah Mada, Yogyakarta, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2019.307

Keywords:

Conditioned medium, Wharton’s jelly stem cells, Hyaluronic acid crosslinking, Transforming growth factor-β1

Abstract

BACKGROUND: Presently, the application of stem cells and their paracrine effect for anti-ageing therapy has commenced. Wharton's jelly-derived stem cell conditioned medium (WJSCs-CM) is renowned for increasing proliferation, migrate ageing skin fibroblasts and increase consumption of extracellular transforming growth factor-β (TGF-β). With more than 85% of frequently used dermal filler procedures are hyaluronic acid fillers (HA), a mixture of both with optimal HA crosslinking degree has not yet been identified.

AIM: This study aimed to determine the discrepancies in the results of various HA crosslinking degree in WJSCs-CM concerning various levels of growth factors (GF).

METHODS: Conditioned medium was obtained from mesenchymal stem cells Wharton’s jelly of the newborn umbilical cord with caesarean section procedure, fabricated with hypoxia method (HCM). HA was obtained from preparations on the market with crosslinking degrees of 3%, 4%, and 10%. GF levels were measured using sandwich ELISA method based on the protocol provided by anti-TGF-β1, platelet-derived growth factor (PDGF), and basic fibroblast growth factor (bFGF) antibody producers (Cloud-Clone Corp®, Texas, USA).

RESULTS: Low degree HA crosslinking (3% and 4%) elevated TGF-β1 release in WJSCs-CM. HA crosslinking did not provoke increased levels of PDGF and bFGF in WJSCs-CM, both at low and higher degrees.

CONCLUSION: Low degree HA crosslinking induced the increase of TGF-β1 release in WJSCs-CM.

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References

Goldman A, Wollina U. Facial rejuvenation for middle-aged women: a combined approach with minimally invasive procedures. Clin Interv Aging. 2010; 5:293-9. https://doi.org/10.2147/CIA.S13215 PMid:20924438 PMCid:PMC2946856

Weihermann AC, Lorencini M, Brohem CA, de Carvalho CM. Elastin structure and its involvement in skin photoageing. Int J Cosmet Sci. 2017; 39(3):241-7. https://doi.org/10.1111/ics.12372 PMid:27731897

Farage MA, Miller KW, Elsner P, Maibach HI. Characteristics of the Aging Skin. Adv Wound Care. 2013; 2(1):5-10. https://doi.org/10.1089/wound.2011.0356 PMid:24527317 PMCid:PMC3840548

Hossain MM, Mukheem A, Kamarul T. The prevention and treatment of hypoadiponectinemia-associated human diseases by up-regulation of plasma adiponectin. Life Sci. 2015; 135:55-67. https://doi.org/10.1016/j.lfs.2015.03.010 PMid:25818192

American Society of Plastic Surgeons. News/Press Release, 2016. Available from: https://www.plasticsurgery.org/documents/News/Statistics/2016/plastic-surgery-statistics-full-report-2016.pdf

Rossignol J, Boyer C, Thinard R, Remy S, Dugast AS, Dubayle D, et al. Mesenchymal stem cells induce a weak immune response in the rat striatum after allo or xenotransplantation. J Cell Mol Med. 2009; 13(8B):2547 58. https://doi.org/10.1111/j.1582-4934.2008.00657.x PMid:20141619

Wirohadidjojo YW, Budiyanto A, Soebono H. Regenerative Effects of Wharton's Jelly Stem Cells-Conditioned Medium in UVA-Irradiated Human Dermal Fibroblasts. Malays J Med Biol Res. 2016; 3:45-50.

Fallacara A, Manfredini S, Durini E, Vertuani S. Hyaluronic Acid Fillers in Soft Tissue Regeneration. Facial Plast Surg. 2017; 33(1):87-96. https://doi.org/10.1055/s-0036-1597685 PMid:28226376

Sclafani AP. Platelet-rich fibrin matrix for improvement of deep nasolabial folds. J Cosmet Dermatol. 2010; 9(1):66-71. https://doi.org/10.1111/j.1473-2165.2010.00486.x PMid:20367676

Kwon TR, Oh CT, Choi EJ, Kim SR, Jang YJ, Ko EJ, et al. Conditioned medium from human bone marrowâ€derived mesenchymal stem cells promotes skin moisturization and effacement of wrinkles in UVBâ€irradiated SKHâ€1 hairless mice. Photodermatol Photoimmunol Photomed. 2016; 32(3):120-8. https://doi.org/10.1111/phpp.12224 PMid:26577060

Elnehrawy NY, Ibrahim ZA, Eltoukhy AM, Nagy HM. Assessment of the efficacy and safety of single platelet-rich plasma injection on different types and grades of facial wrinkles. J Cosmet Dermatol. 2017; 16(1):103-11. https://doi.org/10.1111/jocd.12258 PMid:27474688

Rojas J, Londono C, Ciro Y. The health benefits of natural skin UVA photoprotective compounds found in botanical sources. Int J Pharm Pharm Sci. 2016; 8(3):13-23.

Martinez-Ferrer M, Afshar-Sherif AR, Uwamariya C, de Crombrugghe B, Davidson JM, Bhowmick NA. Dermal Transforming Growth Factor β Responsiveness Mediates Wound Contraction and Epithelial Closure. Am J Pathol. 2010; 176(1):98-107. https://doi.org/10.2353/ajpath.2010.090283 PMid:19959810 PMCid:PMC2797873

Quan T, Wang F, Shao Y, Rittié L, Xia W, Orringer JS, et al. Enhancing structural support of the dermal microenvironment activates fibroblasts, endothelial cells, and keratinocytes in aged human skin in vivo. J Invest Dermatol. 2013; 133(3):658 67. https://doi.org/10.1038/jid.2012.364 PMid:23096713 PMCid:PMC3566280

Fisher GJ, Shao Y, He T, Qin Z, Perry D, Voorhees JJ, et al. Reduction of fibroblast size/mechanical force downâ€regulates TGFâ€Î² type II receptor: implications for human skin aging. Aging Cell. 2016; 15(1):67-76. https://doi.org/10.1111/acel.12410 PMid:26780887 PMCid:PMC4717276

David-Raoudi M, Tranchepain F, Deschrevel B, Vincent JC, Bogdanowicz P, Boumediene K, et al.. Differential effects of hyalorunan and its fragment on fibroblasts: relation to wound healing. Wound Repair Regen. 2008; 16(2):274-87. https://doi.org/10.1111/j.1524-475X.2007.00342.x PMid:18282267

Meran S, Thomas DW, Stephens P, Enoch S, Martin J, Steadman R, et al. Hyaluronan Facilitates Transforming Growth Factor-β1-mediated Fibroblast Proliferation. J Biol Chem. 2008; 283(10):6530-45. https://doi.org/10.1074/jbc.M704819200 PMid:18174158

Arno AI, Amini-Nik S, Blit PH, Al-Shehab M, Belo C, Herer E, et al. Human Wharton's jelly mesenchymal stem cells promote skin wound healing through paracrine signaling. Stem Cell Res Ther. 2014; 5(1):28. https://doi.org/10.1186/scrt417 PMid:24564987 PMCid:PMC4055091

Hariyadi R, Sukardiman, Khotib J. The increasing of VEGF expression and re-epithelialization on dermal wound healing process after treatment of banana peel extract (Musa acuminata Colla). Int J Pharm Pharm Sci. 2014; 6(11):427-30.

Song SY, Jung JE, Jeon YR, Tark KC, Lew DH. Determination of adipose derived stem cell application on photo aged fibroblasts, based on paracrine function. Cytotherapy. 2011; 13(3):378-84. https://doi.org/10.3109/14653249.2010.530650 PMid:21062113

Walter MN, Wright KT, Fuller HR, MacNeil S, Johnson WE. Mesenchymal stem cell conditioned medium accelerates skin wound healing: an in vitro study of fibroblast and keratinocyte scratch assays. Exp Cell Res. 2010; 316(7):1271-81. https://doi.org/10.1016/j.yexcr.2010.02.026 PMid:20206158

Published

2019-05-14

How to Cite

1.
Ariyati N, Kusworini K, Nurdiana N, Wirohadidjojo YW. Low Degree Hyaluronic Acid Crosslinking Inducing the Release of TGF-Β1 in Conditioned Medium of Wharton’s Jelly-Derived Stem Cells. Open Access Maced J Med Sci [Internet]. 2019 May 14 [cited 2024 Apr. 26];7(10):1572-5. Available from: https://oamjms.eu/index.php/mjms/article/view/oamjms.2019.307

Issue

Section

A - Basic Science

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