Suppr超能文献

Ras/细胞外信号调节激酶而非Akt信号通路参与利塞膦酸盐诱导的U937细胞凋亡及其被细胞松弛素B抑制的过程。

Involvement of Ras/extracellular signal-regulated kinase, but not Akt pathway in risedronate-induced apoptosis of U937 cells and its suppression by cytochalasin B.

作者信息

Fujita Hirofumi, Utsumi Toshihiko, Muranaka Shikibu, Ogino Tetsuya, Yano Hiromi, Akiyama Jitsuo, Yasuda Tatsuji, Utsumi Kozo

机构信息

Institute of Medical Science, Kurashiki Medical Center, Kurashiki 710-8522, Japan.

出版信息

Biochem Pharmacol. 2005 Jun 15;69(12):1773-84. doi: 10.1016/j.bcp.2005.03.006.

Abstract

Although risedronate, a nitrogen containing bisphosphonate (BPs), strongly inhibits bone resorption by enhanced apoptosis of osteoclasts, its mechanism remained unclear. In this study, we investigated the molecular mechanism of risedronate-induced apoptosis of U937 cells, with a focus on extracellular signal-regulated kinase 1/2 (ERK 1/2) and protein kinase B (Akt) pathways, mitochondria-mediated apoptosis, and the effect of disruption of the actin cytoskeleton. Risedronate facilitated the relocation of Ras from membrane to cytosol through inhibited isoprenylation. Accordingly, risedronate suppressed the phosphorylation of ERK 1/2, a downstream survival signaling kinase of Ras, affected the intracellular distribution of Bcl-xL, and induced the mitochondrial membrane depolarization, cytochrome c release, activated caspase cascade and DNA fragmentation. The risedronate-induced apoptosis was effectively suppressed with cyclosporine A plus trifluoperazine, potent inhibitors of mitochondrial membrane permeability transition (MPT). The risedronate-induced apoptosis was independent of Akt, another cAMP-dependent survival signaling kinase. Risedronate facilitated dephosphorylation of Bad at Ser112, an ERK phosphorylation site, but not at Ser136, an Akt phosphorylation site. All of these apoptosis-related changes induced by risedronate were strongly suppressed by cytochalasin B, an inhibitor of actin filament polymerization. These results indicate that risedronate-induced apoptosis in U937 cells involves Ras/ERK, but not Akt signaling pathway, and is dependent on MPT, and that disruption of the actin cytoskeleton inhibits the risedronate-induced apoptosis at its early step.

摘要

尽管含氮双膦酸盐(BPs)利塞膦酸盐通过增强破骨细胞凋亡来强烈抑制骨吸收,但其机制仍不清楚。在本研究中,我们研究了利塞膦酸盐诱导U937细胞凋亡的分子机制,重点关注细胞外信号调节激酶1/2(ERK 1/2)和蛋白激酶B(Akt)信号通路、线粒体介导的凋亡以及肌动蛋白细胞骨架破坏的影响。利塞膦酸盐通过抑制异戊二烯化促进Ras从膜向胞质溶胶的重新定位。相应地,利塞膦酸盐抑制了Ras的下游存活信号激酶ERK 1/2的磷酸化,影响了Bcl-xL的细胞内分布,并诱导线粒体膜去极化、细胞色素c释放、激活半胱天冬酶级联反应和DNA片段化。环孢素A加三氟拉嗪(线粒体膜通透性转换(MPT)的有效抑制剂)可有效抑制利塞膦酸盐诱导的凋亡。利塞膦酸盐诱导的凋亡独立于另一种cAMP依赖性存活信号激酶Akt。利塞膦酸盐促进了Bad在Ser112(一个ERK磷酸化位点)的去磷酸化,但在Ser136(一个Akt磷酸化位点)未促进其去磷酸化。利塞膦酸盐诱导的所有这些凋亡相关变化均被肌动蛋白丝聚合抑制剂细胞松弛素B强烈抑制。这些结果表明,利塞膦酸盐诱导U937细胞凋亡涉及Ras/ERK信号通路,但不涉及Akt信号通路,且依赖于MPT,并且肌动蛋白细胞骨架的破坏在早期阶段抑制了利塞膦酸盐诱导的凋亡。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验