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|Title:||The role of the activin system in keloid pathogenesis|
|Keywords:||α-smooth muscle actin|
Transforming growth factor-β
|Citation:||Mukhopadhyay, A., Sui, Y.C., Lim, I.J., Phillips, D.J., Phan, T.T. (2007-04). The role of the activin system in keloid pathogenesis. American Journal of Physiology - Cell Physiology 292 (4) : C1331-C1338. ScholarBank@NUS Repository. https://doi.org/10.1152/ajpcell.00373.2006|
|Abstract:||Keloid scars represent a pathological response to cutaneous injury under the regulation of many growth factors. Activin-A, a dimeric protein and a member of the transforming growth factor-β superfamily, has been shown to regulate various aspects of cell growth and differentiation in the repair of the skin mesenchyme and the epidermis. Thus our aim was to study the role of activin and its antagonist, follistatin, in keloid pathogenesis. Increased mRNA expression for activin was observed in keloid scar tissue by performing RNase protection assay. Immunohistochemistry showed increased localization of both activin-A and follistatin in the basal layer of epidermis of keloid tissue compared with normal tissue. ELISA demonstrated a 29-fold increase in concentration of activin-A and an ≃5-fold increase in follistatin in conditioned media in keloid fibroblasts compared with normal fibroblasts. Although keloid keratinocytes produced 25% more follistatin than normal keratinocytes, the amounts of activin-A, in contrast, was ≃77% lower. Proliferation of fibroblasts was stimulated when treated with exogenous activin-A (46% increase in keloids fibroblasts) or following co-culture with hβAHaCaT cells (66% increase). Activin-A upregulated key extracellular matrix components, namely collagen, fibronectin, and α-smooth muscle actin, in normal and keloid fibroblasts. Co-treatment of follistatin with activin-A blocked the stimulatory effects of activin on extracellular matrix components. These findings emphasize the importance of the activin system in keloid biology and pathogenesis and suggest a possible therapeutic potential of follistatin in the prevention and treatment of keloids. Copyright © 2007 the American Physiological Society.|
|Source Title:||American Journal of Physiology - Cell Physiology|
|Appears in Collections:||Staff Publications|
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