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ORIGINAL RESEARCH

Proteomic Identification and Quantification of Secretory Proteins in Human Dermal Fibroblast-Conditioned Medium for Wound Repair and Hair Regeneration

, ORCID Icon, ORCID Icon, & ORCID Icon
Pages 1145-1157 | Received 18 Feb 2023, Accepted 27 Apr 2023, Published online: 01 May 2023

References

  • Lawlor KT, Kaur P. Dermal contributions to human interfollicular epidermal architecture and self-renewal. Int J Mol Sci. 2015;16:28098–28107. doi:10.3390/ijms161226078
  • Leary T, Jones PL, Appleby M, Blight A, Parkinson K, Stanley M. Epidermal keratinocyte self-renewal is dependent upon dermal integrity. J Invest Dermatol. 1992;99:422–430. doi:10.1111/1523-1747.ep12616134
  • Tuan TL, Keller LC, Sun D, Nimni ME, Cheung D. Dermal fibroblasts activate keratinocyte outgrowth on collagen gels. J Cell Sci. 1994;107:2285–2289. doi:10.1242/jcs.107.8.2285
  • Sorrell JM, Baber MA, Caplan AI. Site-matched papillary and reticular human dermal fibroblasts differ in their release of specific growth factors/cytokines and in their interaction with keratinocytes. J Cell Physiol. 2004;200:134–145. doi:10.1002/jcp.10474
  • Maarof M, Lokanathan Y, Ruszymah HI, Saim A, Chowdhury SR. Proteomic analysis of human dermal fibroblast conditioned medium (DFCM). Protein J. 2018;37:589–607. doi:10.1007/s10930-018-9800-z
  • Kubo K, Kuroyanagi Y. A study of cytokines released from fibroblasts in cultured dermal substitute. Artif Organs. 2005;29:845–849. doi:10.1111/j.1525-1594.2005.00138.x
  • Chowdhury SR, Aminuddin BS, Ruszymah BH. Effect of supplementation of dermal fibroblasts conditioned medium on expansion of keratinocytes through enhancing attachment. Indian J Exp Biol. 2012;50:332–339.
  • Shin JM, Lee YY, Kim KM, et al. The potential role of fibroblast-derived multi-peptide factors in activation of growth factors and β-catenin in hair follicle cells. J Cosmet Dermatol. 2022;21:6184–6190. doi:10.1111/jocd.15188
  • Yun SH, Park GW, Kim JY, et al. Proteomic characterization of the Pseudomonas putida KT2440 global response to a monocyclic aromatic compound by iTRAQ analysis and 1DE-MudPIT. J Proteomics. 2011;74:620–628.
  • Choi CW, Lee YG, Kwon SO, et al. Analysis of Streptococcus pneumoniae secreted antigens by immuno-proteomic approach. Diagn Microbiol Infect Dis. 2012;72:318–327. doi:10.1016/j.diagmicrobio.2011.12.013
  • Thio CL, Yusof R, Ashrafzadeh A, Bahari S, Abdul-Rahman PS, Karsani SA. Differential analysis of the secretome of WRL68 cells infected with the Chikungunya virus. PLoS One. 2015;10:e0129033. doi:10.1371/journal.pone.0129033
  • Creaney J, Dick IM, Leon JS, Robinson BW. A proteomic analysis of the malignant mesothelioma secretome using iTRAQ. Cancer Genomics Proteomics. 2017;14:103–117.
  • Lee SY, Kim DY, Suh SB, Suh JY, Cho SB. Effects of human fibroblast-derived multi-peptide factors on the proliferation and migration of nitrogen plasma-treated human dermal fibroblasts. Clin Cosmet Investig Dermatol. 2022;15:2465–2475. doi:10.2147/CCID.S383483
  • DiPersio CM, Zheng R, Kenney J, Van De Water L. Integrin-mediated regulation of epidermal wound functions. Cell Tissue Res. 2016;365:467–482. doi:10.1007/s00441-016-2446-2
  • Couture C, Desjardins P, Zaniolo K, Germain L, Guérin SL. Enhanced wound healing of tissue-engineered human corneas through altered phosphorylation of the CREB and AKT signal transduction pathways. Acta Biomater. 2018;73:312–325. doi:10.1016/j.actbio.2018.04.021
  • Abreu-Blanco MT, Verboon JM, Parkhurst SM. Coordination of Rho family GTPase activities to orchestrate cytoskeleton responses during cell wound repair. Curr Biol. 2014;24:144–155. doi:10.1016/j.cub.2013.11.048
  • Nakamura M, Verboon JM, Parkhurst SM. Prepatterning by RhoGEFs governs Rho GTPase spatiotemporal dynamics during wound repair. J Cell Biol. 2017;216:3959–3969. doi:10.1083/jcb.201704145
  • Hu L, Wang J, Zhou X, et al. Exosomes derived from human adipose mensenchymal stem cells accelerates cutaneous wound healing via optimizing the characteristics of fibroblasts. Sci Rep. 2016;6:32993. doi:10.1038/srep32993
  • Nelson WJ, Nusse R. Convergence of Wnt, beta-catenin, and cadherin pathways. Science. 2004;303:1483–1487. doi:10.1126/science.1094291
  • Yang HL, Tsai YC, Korivi M, Chang CT, Hseu YC. Lucidone promotes the cutaneous wound healing process via activation of the PI3K/AKT, Wnt/β-catenin and NF-κB signaling pathways. Biochim Biophys Acta Mol Cell Res. 2017;1864:151–168. doi:10.1016/j.bbamcr.2016.10.021
  • Ito M, Yang Z, Andl T, et al. Wnt-dependent de novo hair follicle regeneration in adult mouse skin after wounding. Nature. 2007;447:316–320. doi:10.1038/nature05766
  • Cho SB, Goo BL, Zheng Z, Yoo KH, Kang JS, Kim H. Therapeutic efficacy and safety of a 1927-nm fractionated thulium laser on pattern hair loss: an evaluator-blinded, split-scalp study. Lasers Med Sci. 2018;33:851–859. doi:10.1007/s10103-018-2437-5
  • Yang Z, Ma S, Cao R, et al. CD49fhigh defines a distinct skin mesenchymal stem cell population capable of hair follicle epithelial cell maintenance. J Invest Dermatol. 2020;140:544–555.e9. doi:10.1016/j.jid.2019.08.442
  • Maarof M, Chowdhury SR, Saim A, Bt Hj Idrus R, Lokanathan Y. Concentration dependent effect of human dermal fibroblast conditioned medium (DFCM) from three various origins on keratinocytes wound healing. Int J Mol Sci. 2020;21:2929. doi:10.3390/ijms21082929
  • Lago JC, Puzzi MB. The effect of aging in primary human dermal fibroblasts. PLoS One. 2019;14:e0219165. doi:10.1371/journal.pone.0219165
  • Temiz SA, Dursun R. Dermatolojide plateletten zengin plazma tedavisi. Selcuk Med J. 2020;36:274–281.
  • Li ZJ, Choi HI, Choi DK, et al. Autologous platelet-rich plasma: a potential therapeutic tool for promoting hair growth. Dermatol Surg. 2012;38:1040–1046. doi:10.1111/j.1524-4725.2012.02394.x