Acta Med. 2005, 48: 137-144
https://doi.org/10.14712/18059694.2018.41
Expression of Cytoskeletal Proteins in Hepatic Stellatecells Isolated from Normal and Cirrhotic Rat Liver
References
1. Hepatology 1998; 28:404–411.
< M, Baringhaus KH, Gerl M, Günzler V, Kanta J, Schmidts L, Stapf M, Tschank G, Weidman K, Werner U. Selective inihibition of hepatic collagen accumulation in experimental liver fibrosis in rats by a new prolyl 4–hydroxylase inhibitor. https://doi.org/10.1002/hep.510280217>
2. Biol Cell 1996; 87:65–73.
< G, Hamprecht B, Gebhardt R. Glial fibrillary acidic protein as a marker of perisinusoidal stellate cells that can distinguish between the normal and myofibroblast- like phenotypes. https://doi.org/10.1111/j.1768-322X.1996.tb00967.x>
3. Hepatology 1999; 30:761–769.
< AM, Wright MC, Hay RT, Arthur MJP, Hughes T, Bahr MJ, Degitz K, Mann DA. Persistent activation of nuclear factor-κB in cultured rat hepatic stellate cells involves the induction of potentially novel Rel-like factors and prolonged changes in the expression of IκB family proteins. https://doi.org/10.1002/hep.510300327>
4. J Biol Chem 1989; 264:10756–10762.
SL, Roll FJ, Bozles J, Arenson DM, Bissell DM. Maintenance of differentiated phenotype of cultured rat hepatic lipocytes by basement membrane matrix.
5. New England J Med 1993; 328:1828–1835.
< SL. The cellular basis of hepatic fibrosis. Mechanisms and treatment strategies. https://doi.org/10.1056/NEJM199304223281620>
6. J Hepatol 1989; 9:59–68.
< A, Vrijsen R, Rauterberg J, Burt A, Schellinck, Wisse E. In vitro differentiation of fat-storing cells parallels marked increase of collagen synthesis and secretion. https://doi.org/10.1016/0168-8278(89)90076-7>
7. Hepatology 1998; 27:590–598.
< A, Niki T, Hellemans K, De Craemer D, Van Den Berg K, Lazou JM, Stange G, Van De Winkel, De Bleser P. Purification of rat hepatic stellate cells by side scatter-activated cell sorting. https://doi.org/10.1002/hep.510270238>
8. Cell Tissue Res 1998; 292:447–452.
< AM. The cell biology of liver fibrogenesis – an imbalance of proliferation, growth arrest and apoptosis of myofibroblasts. https://doi.org/10.1007/s004410051073>
9. Exp Cell Res 1982; 139:468–472.
< DL, Sefelaar AM, de Leeuw. Fat-storing cells of the rat liver. https://doi.org/10.1016/0014-4827(82)90283-X>
10. Li D, Friedman SL. Hepatic stellate cells: morphology, function, and regulation. In: Arias IM, Boyer JL, Chisari FV, Fausto N, Schachter D, Shafritz DA, eds. The Liver: Biology and Pathobiology. Philadelphia: Lippincott Williams and Wilkins, 2001: 455–468.
11. Hepato-Gastroenterol 1996; 43:72–91.
J, Geerts A, Burt AD. Pathobiology of hepatic stellate cells.
12. J Hepatol 1996; 24:719–730.
< K, Knittel T, Aurisch S, Fellmer P, Ramadori G.. Glial fibrillary acidic protein – a cell type specific marker for Ito cells in vivo and in vitro. https://doi.org/10.1016/S0168-8278(96)80269-8>
13. Exp Cell Res 2004; 301:1–7.
< D, Li Z. Desmin: a major intermediate filament protein essential for the structural integrity and function of muscle. https://doi.org/10.1016/j.yexcr.2004.08.004>
14. Hepatology 1983; 3:112–120.
< R. Is cirrhosis of the liver experimentally produced by CCl4 an adequate model of human cirrhosis? https://doi.org/10.1002/hep.1840030118>
15. Pharmac Ther 1995; 66:387–412.
< M. Novel insights into the biology and physiology of the Ito cell. https://doi.org/10.1016/0163-7258(94)00072-B>
16. Semin Liver Dis 1999; 19:397–410.
< M, Gentilini P. Biology of hepatic stellate cells and their possible relevance in the pathogenesis of portal hypertension in cirrhosis. https://doi.org/10.1055/s-2007-1007128>
17. Virchows Arch B Cell Pathol 1990; 59:349–357.
< G, Veit T, Schwögler S, Dienes HP, Knittel T, Rieder H, Meyer zum Büschenfelde KH. https://doi.org/10.1007/BF02899424>
18. Cell Motil Cytoskeleton 1992; 22:227–234.
< DC, Friedman SL. Cytoskeleton of liver perisinusoidal cells (lipocytes) in normal and pathological conditions. https://doi.org/10.1002/cm.970220402>
19. Med Electron Microsc 2004; 37:3–15.
< H. Structure and function of hepatic stellate cells. https://doi.org/10.1007/s00795-003-0230-3>
20. J Cell Biol 1991; 112:1205–1213.
< DE, Shelanski ML, Liem RKH. Suppression by antisense mRNA demonstrates a requirement for the glial fibrillary acidic protein in the formation of stable astrocytic processes in response to neurons. https://doi.org/10.1083/jcb.112.6.1205>
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