Literature DB >> 12007718

Differences in collagen production between normal and keloid-derived fibroblasts in serum-media co-culture with keloid-derived keratinocytes.

Toan-Thang Phan1, Ivor J Lim, Boon-Huat Bay, Robert Qi, Hung T Huynh, Seng-Teik Lee, Michael T Longaker.   

Abstract

Keloids are characterized by the deposition of excessive extracellular-matrix collagen by abnormal fibroblasts in response to cutaneous injury. Studies to date have largely concentrated on the role of the keloid fibroblast in the pathogenesis of this lesion. Recent studies have highlighted the important concept of epithelial-mesenchymal interactions in normal skin biology. Extrapolating this to keloids in two recent serum-free in vitro studies, we demonstrated increased growth and proliferation, as well as induction of keloid-like collagen secretory characteristics in normal fibroblasts co-cultured with keloid-derived keratinocytes. Most fibroblast culture work to date has been performed in nutrient and growth factor-rich serum media. To investigate how a serum co-culture system might influence epithelial-mesenchymal interactions, [3H] proline incorporation was examined in normal and keloid fibroblasts co-cultured in serum with keratinocytes derived either from normal skin or keloid tissue. Results showed increased [3H] proline incorporation when normal fibroblasts were co-cultured with keloid keratinocytes, which was significantly increased when keloid fibroblasts were co-cultured with keloid keratinocytes. Taken with previous results, this study demonstrates a good correlation between both serum and serum-free co-culture systems, and supports the significance of epithelial-mesenchymal interactions in keloid pathogenesis.

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Year:  2002        PMID: 12007718     DOI: 10.1016/s0923-1811(02)00008-7

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  7 in total

1.  Cell permeant peptide analogues of the small heat shock protein, HSP20, reduce TGF-beta1-induced CTGF expression in keloid fibroblasts.

Authors:  Luciana B Lopes; Elizabeth J Furnish; Padmini Komalavilas; Charles R Flynn; Patricia Ashby; Adam Hansen; Daphne P Ly; George P Yang; Michael T Longaker; Alyssa Panitch; Colleen M Brophy
Journal:  J Invest Dermatol       Date:  2008-09-11       Impact factor: 8.551

2.  5-Fluorouracil treatment of problematic scars.

Authors:  Mounir J Haurani; Kenneth Foreman; James J Yang; Aamir Siddiqui
Journal:  Plast Reconstr Surg       Date:  2009-01       Impact factor: 4.730

Review 3.  Low-dose enalapril in the treatment of surgical cutaneous hypertrophic scar and keloid--two case reports and literature review.

Authors:  Silvai Iannello; Paolina Milazzo; Fabio Bordonaro; Francesco Belfiore
Journal:  MedGenMed       Date:  2006-12-20

4.  Pirfenidone inhibits epithelial-mesenchymal transition in keloid keratinocytes.

Authors:  Latha Satish; Alexander Evdokiou; Eleni Geletu; Jennifer M Hahn; Dorothy M Supp
Journal:  Burns Trauma       Date:  2020-02-27

5.  Keloid-derived keratinocytes acquire a fibroblast-like appearance and an enhanced invasive capacity in a hypoxic microenvironment in vitro.

Authors:  Xiaoyang Ma; Jia Chen; Bei Xu; Xiao Long; Han Qin; Robert Chunhua Zhao; Xiaojun Wang
Journal:  Int J Mol Med       Date:  2015-03-13       Impact factor: 4.101

Review 6.  Regeneration of Dermis: Scarring and Cells Involved.

Authors:  Alexandra L Rippa; Ekaterina P Kalabusheva; Ekaterina A Vorotelyak
Journal:  Cells       Date:  2019-06-18       Impact factor: 6.600

Review 7.  The Keloid Disorder: Heterogeneity, Histopathology, Mechanisms and Models.

Authors:  Grace C Limandjaja; Frank B Niessen; Rik J Scheper; Susan Gibbs
Journal:  Front Cell Dev Biol       Date:  2020-05-26
  7 in total

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