Abstract
Many studies have described changes in the hepatic extracellular matrix (ECM) and the cells involved in its production during liver injury [1, 2]. In acute liver damage, there may be complete parenchymal regeneration, scar formation, or a combination of both, and fibrogenesis seems to be transient [3]. Several cells of the liver can produce various ECM components. However, the hepatic stellate cell (HSC, also known as Ito or fat-storing cell) is the main source of ECM [24, 25] and has been shown to play a role in fibrogenesis for wound repair in acute injury of the liver [2, 18]. The HSCs can proliferate and rapidly express α smooth muscle (SM) actin, which is indicative of the cell’s involvement in matrix deposition [2, 25–27].
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Tuchweber, B., Desmoulière, A., Costa, A.M.A., Yousef, I.M., Gabbiani, G. (1999). Myofibroblastic Differentiation and Extracellular Matrix Deposition in Early Stages of Cholestatic Fibrosis in Rat Liver. In: Desmoulière, A., Tuchweber, B. (eds) Tissue Repair and Fibrosis. Current Topics in Pathology, vol 93. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-58456-5_11
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DOI: https://doi.org/10.1007/978-3-642-58456-5_11
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