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Title: Investigation of keratinocyte regulation of collagen I synthesis by dermal fibroblasts in a simple in vitro model
Authors: Harrison, C.A.
Gossiel, F.
Bullock, A.J.
Sun, Tao
Blumsohn, A.
MacNeil, Sheila
Issue Date: 2006
Publisher: © Wiley
Citation: HARRISON, C.A, 2006. Investigation of keratinocyte regulation of collagen I synthesis by dermal fibroblasts in a simple in vitro model. British Journal of Dermatology, 154 (3), pp.401-410
Abstract: Background  Hypertrophic scarring and skin graft contracture are major causes of morbidity after burn injuries. A prominent feature is excessive fibroplasia with accumulation of increased fibrillar collagen relative to normal scar tissue. The application of split-thickness skin grafts or cultured epithelial autografts to burn wounds is known to reduce scarring and contraction. Objectives  To investigate further how the keratinocyte influences underlying fibroblast behaviour by examining the influence of keratinocytes on fibroblast collagen synthesis, using a new assay for collagen synthesis never previously applied to skin cell biology. Methods  We investigated the influence of the keratinocyte on fibroblast synthesis of type I collagen using an immunoassay for the aminoterminal propeptide of type I collagen (P1NP) in conditioned medium from monocultures and cocultures of keratinocytes and fibroblasts over 14 days. The importance of the physical presence of the keratinocyte was investigated by comparing cocultures of keratinocytes and fibroblasts against fibroblast monocultures with keratinocyte-conditioned medium. Pharmacological agents known to promote fibroblast proliferation [basic fibroblast growth factor (bFGF)], keratinocyte proliferation [insulin-like growth factor (IGF)-1], modify scarring in vivo[tumour necrosis factor (TNF)-α] or modify collagen biochemistry [putrescine, estrone, estradiol and β-aminopropionitrile (β-APN)] were then investigated for their effect on collagen synthesis in fibroblasts and in keratinocyte/fibroblast cocultures. Results  Keratinocytes in coculture with fibroblasts, and keratinocyte-conditioned medium, both reduced fibroblast P1NP synthesis. Of the pharmacological agents investigated, bFGF, IGF-1, TNF-α and β-APN all increased collagen synthesis both in monocultures of fibroblasts and in cocultures of keratinocytes and fibroblasts. Conclusions  Fibroblast collagen synthesis appears to be downregulated by keratinocyte-derived cytokines. Fibroblast growth factors and proinflammatory cytokines appear to be able partially to overcome this downregulation and to increase collagen synthesis.
Description: This paper is closed access.
Version: Closed access
DOI: 10.1111/j.1365-2133.2005.07022.x
URI: https://dspace.lboro.ac.uk/2134/24968
Publisher Link: http://dx.doi.org/10.1111/j.1365-2133.2005.07022.x
ISSN: 0007-0963
Appears in Collections:Closed Access (Chemical Engineering)

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