Long-term Forskolin Stimulation Induces AMPK Activation and Thereby Enhances Tight junction Formation in Human Placental Trophoblast BeWo Cells

被引:32
作者
Egawa, M. [1 ]
Kamata, H. [1 ]
Kushiyama, A. [2 ]
Sakoda, H. [3 ,4 ]
Fujishiro, M. [3 ,4 ]
Horike, N. [4 ,5 ]
Yoneda, M. [1 ]
Nakatsu, Y. [1 ]
Ying, Guo [1 ]
Jun, Zhang [1 ]
Tsuchiya, Y. [1 ]
Takata, K. [6 ]
Kurihara, H. [4 ,5 ]
Asano, T. [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Div Mol & Med Sci, Dept Med Chem,Minami Ku, Hiroshima 7348551, Japan
[2] Asahi Life Fdn, Inst Adult Dis, Tiyoda Ku, Tokyo 1000005, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Internal Med, Bunkyo Ku, Tokyo 1130033, Japan
[4] Univ Tokyo, Fac Med, Bunkyo Ku, Tokyo 1130033, Japan
[5] Univ Tokyo, Grad Sch Med, Dept Physiol Chem & Metab, Tokyo 1130033, Japan
[6] Gunma Univ, Dept Cell Biol, Inst Cellular & Mol Regulat, Gunma 3718512, Japan
关键词
BeWo cells; Forskolin; Tight junction; AMPK;
D O I
10.1016/j.placenta.2008.09.008
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
BeWo cells, derived from human choriocarcinoma, have been known to respond to forskolin or cAMP analogues by differentiating into multinucleated cells- like syncytiotrophoblasts on the surfaces of chorionic villi of the human placenta. In this study, we demonstrated that long-term treatment with forskolin enhances the tight junction (TJ) formation in human placental BeWo cells. Interestingly, AMPK activation and phosphorylation of acetyl-CoA carboxylase (ACC), a molecule downstream from AMPK, were induced by long-term incubation (> 12 h) with forskolin, despite not being induced by acute stimulation with forskolin. In addition, co-incubation with an AMPK inhibitor, compound C, as well as overexpression of an AMPK dominant negative Mutant inhibited forskolin-induced TJ formation. Thus, although the molecular mechanism underlying AMPK activation via the forskolin Stimulation is unclear, the TJ formation induced by forskolin is likely to be mediated by the AMPK pathway. Taking into consideration that TJs are present in the normal human placenta, this mechanism may be important for forming the placental barrier system between the fetal and maternal circulations. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1003 / 1008
页数:6
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