Kruidering M, van de Water B, Zhan Y, Baelde J J, Heer E, Mulder G J, Stevens J L, Nagelkerke J F
Division of Toxicology, Leiden/Amsterdam Center for Drug Research, Leiden University, P.O. Box 9503, 2300 RA Leiden, The Netherlands.
Cell Death Differ. 1998 Jul;5(7):601-14. doi: 10.1038/sj.cdd.4400392.
In primary cultures of porcine proximal tubular kidney cells and LLC-PK1 cells cisplatin (5 - 50 microM) caused apoptosis and cell detachment; in both systems cell detachment occurred, preceded by a loss of cytoskeletal F-actin stress fibers within 4 - 6 h, and a reduction of mRNA encoding for fibronectin, collagen a2 type (IV) and laminin B2 within 17 - 41 h. Prevention of F-actin damage by phalloidin prevented nuclear fragmentation, suggesting a relation between F-actin damage and apoptosis. Overexpression of Bcl-2 also prevented apoptosis, but did not prevent damage to the F-actin skeleton or the reduction of mRNA expression of the matrix proteins. These results suggest that Bcl-2 overexpression interferes with apoptotic signals downstream of F-actin. The relevance of these results for cell detachment in kidney toxicity is discussed.
在猪近端肾小管细胞和LLC - PK1细胞的原代培养中,顺铂(5 - 50微摩尔)可导致细胞凋亡和脱落;在这两个系统中,细胞均出现脱落,在4 - 6小时内细胞骨架F - 肌动蛋白应力纤维丧失,在17 - 41小时内纤连蛋白、IV型胶原α2和层粘连蛋白B2的编码mRNA减少。用鬼笔环肽预防F - 肌动蛋白损伤可防止核碎裂,提示F - 肌动蛋白损伤与细胞凋亡之间存在关联。Bcl - 2的过表达也可防止细胞凋亡,但不能防止F - 肌动蛋白骨架的损伤或基质蛋白mRNA表达的降低。这些结果表明,Bcl - 2过表达干扰了F - 肌动蛋白下游的凋亡信号。文中讨论了这些结果与肾脏毒性中细胞脱落的相关性。