Dhanabal M, Ramchandran R, Waterman M J, Lu H, Knebelmann B, Segal M, Sukhatme V P
Renal Division, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215, USA.
J Biol Chem. 1999 Apr 23;274(17):11721-6. doi: 10.1074/jbc.274.17.11721.
Endostatin, a carboxyl-terminal fragment of collagen XVIII, has been shown to regress tumors in mice. In this study, we have analyzed the mechanism of endostatin action on endothelial cells and nonendothelial cells. Endostatin treatment of cow pulmonary artery endothelial cells caused apoptosis, as demonstrated by three methods, annexin V-fluorescein isothiocyanate staining, caspase 3, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end-labeling assay. Moreover, addition of endostatin led to a marked reduction of the Bcl-2 and Bcl-XL anti-apoptotic protein, whereas Bax protein levels were unaffected. These effects were not seen in several nonendothelial cells. Collectively, these findings provide important mechanistic insight into endostatin action.
内皮抑素是胶原蛋白 XVIII 的羧基末端片段,已被证明可使小鼠肿瘤消退。在本研究中,我们分析了内皮抑素作用于内皮细胞和非内皮细胞的机制。用三种方法(膜联蛋白 V-异硫氰酸荧光素染色、半胱天冬酶 3 和末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记分析)证明,用内皮抑素处理牛肺动脉内皮细胞会导致细胞凋亡。此外,添加内皮抑素会导致抗凋亡蛋白 Bcl-2 和 Bcl-XL 显著减少,而 Bax 蛋白水平未受影响。在几种非内皮细胞中未观察到这些效应。总的来说,这些发现为内皮抑素的作用机制提供了重要的见解。