Browsing by Author "Lin, Chia-Ying"

Now showing 1 - 6 of 6

Mammalian Ste20-like protein kinase 3 induces a caspase-independent apoptotic pathway
(2010-01-01)
Lin, Chia-Ying
;
Wu, Hung-Yi
;
Wang, Pei-Ling
;
Yuan, Chiun-Jye
;
生物科技學系
In this study, it was shown that the mammalian sterile 20-like serine/threonine protein kinase 3 (Mst3) plays an essential role in the staurosporine-induced apoptosis of HeLa cells. The staurosporine-induced apoptosis was reduced by around 65% by the selective knockdown of Mst3 in stable clones, HeLa(siMst3). Although caspases were shown to be involved in the Mst3-mediated apoptosis, only 15-20% of staurosporine-induced apoptosis was suppressed by the caspase inhibitor, z-DEVD-fmk. Accordingly, Mst3 was proposed to trigger a caspase-independent apoptotic pathway in response to staurosporine. Interestingly, staurosporine greatly induced the mitochondrial membrane potential transition in HeLa cells, but had no effect in Hela(siMst3). The role of Mst3 in controlling the mitochondrial integrity was therefore proposed, presumably through the regulation of Bax. Furthermore, it was shown that staurosporine promoted the nuclear translocation of apoptosis-inducing factor and endonuclease G in HeLa cells. The nuclease activity associated with endonuclease G was also enhanced in response to staurosporine. However, both staurosporine-induced nuclear translocation of apoptosis-inducing factor and endonuclease G and the nuclease activity associated with endonuclease G were markedly reduced in Hela(siMst3). These results suggest that Mst3 may respond to staurosporine to trigger the caspase-independent apoptotic pathway by regulating the nuclear translocation of apoptosis-inducing factor and endonuclease G, and the nuclease activity associated with endonuclease G. (C) 2009 Elsevier Ltd. All rights reserved.
Mammalian Ste20-like protein kinase 3 mediates trophoblast apoptosis in spontaneous delivery
(2008-02-01)
Wu, Hung-Yi
;
Lin, Chia-Ying
;
Lin, Tze-Yi
;
Chen, Tai-Chang
;
Yuan, Chiun-Jye
The placenta is essential in transferring gases and nutrients from the mother to the developing fetus. Trophoblast apoptosis may cause labor or other pregnancy-related disorders. This study demonstrated the essential role of Mst3, a human Ste20-like protein kinase, in the oxidative stress-induced apoptosis of trophoblasts of term placenta in normal spontaneous delivery. Oxidative stress, but not hormones released during labor such as prostaglandin E-1, oxytocin or angiotensin II, induces the expression of Mst3 and apoptosis of human term placenta after elective Cesarean section without labor pain. The role of Mst3 in oxidative stress-induced apoptosis was further demonstrated in the 3A-sub-E, a human trophoblast cell line. The H2O2-induced apoptosis of 3A-sub-E cells was largely suppressed by overexpressed Mst3(KR), the kinase-dead mutant or by selective knockdown of endogenous Mst3. Further studies showed that Jun N-terminal kinase (JNK) may participate in the signaling pathway of H2O2-induced apoptosis by mediating the level of Mst3. Subsequently, caspase 3 and other downstream apoptotic components may be activated by Mst3 and trigger the apoptotic process in human trophoblasts.
Mammalian Ste20-like protein kinase 3 plays a role in hypoxia-induced apoptosis of trophoblast cell line 3A-sub-E
(2011-05-01)
Wu, Hung-Yi
;
Lin, Chia-Ying
;
Chen, Tai-Chang
;
Pan, Shien-Tung
;
Yuan, Chiun-Jye
Mammalian Ste20-like protein kinase 3 (Mst3) is a key player in inducing apoptosis in a variety of cell types and has recently been shown to participate in the signaling pathway of hypoxia-induced apoptosis of human trophoblast cell line 3A-sub-E (3A). It is believed that oxidative stress may occur during hypoxia and induce the expression of Mst3 in 3A cells via the activation of c-Jun N-terminal protein kinase 1 (JNK1). This hypothesis was demonstrated by the suppressive effect of DL-alpha-lipoic acid, a reactive oxygen species scavenger, in hypoxia-induced responses of 3A cells such as Mst3 expression, nitrotyrosine formation. JNK1 activation and apoptosis. Similar results were also observed in trophoblasts of human placental explants in both immunohistochemical studies and immunoblot analyses. These suggested that the activation of Mst3 might trigger the apoptotic process in trophoblasts by activating caspase 3 and possibly other apoptotic pathways. The role of nitric oxide synthase (NOS) and NADPH oxidase (NOX) in hypoxia-induced Mst3 up-regulation was also demonstrated by the inhibitory effect of N(G)-nitro-L-arginine and apocynin, which inhibits NOS and NOX, respectively. Oxidative stress was postulated to be induced by NOS and NOX in 3A cells during hypoxia. In conclusion, hypoxia induces oxidative stress in human trophoblasts by activating NOS and NOX. Subsequently, Mst3 is up-regulated and plays an important role in hypoxia-induced apoptosis of human trophoblasts. (C) 2011 Elsevier Ltd. All rights reserved.
Mst3 Plays an Important Role in Hypoxia-induced placental Apoptosis in Preeclampsia
(2009-04-01)
Yuan, Chiun-Jye
;
Wu, Hung-Yi
;
Lin, Chia-Ying
;
生物科技學系
;
Department of Biological Science and Technology
Mst3 plays an important role in the hypoxia-induced apoptosis of human trophoblasts
(2010-04-01)
Wu, Hung-Yi
;
Lin, Chia-Ying
;
Pan, Shien-Tung
;
Yuan, Chiun-Jye
;
交大名義發表
Role of Mst3 in oxidative phosphorylation
(2010-04-01)
Lin, Chia-Ying
;
Wu, Hung-Yi
;
Yuan, Chiun-Jye
;
交大名義發表
;
National Chiao Tung University