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凋亡调控因子 Nrz 通过调节斑马鱼囊胚期的 Ca2+ 转运来控制细胞骨架动力学。

The apoptotic regulator Nrz controls cytoskeletal dynamics via the regulation of Ca2+ trafficking in the zebrafish blastula.

机构信息

CRCL U1052 INSERM, UMS 3443 CNRS, Centre Léon Bérard, 28 rue Laennec, 69008 Lyon, France.

出版信息

Dev Cell. 2011 May 17;20(5):663-76. doi: 10.1016/j.devcel.2011.03.016.

Abstract

Bcl-2 family members are key regulators of apoptosis. Their involvement in other cellular processes has been so far overlooked. We have studied the role of the Bcl-2 homolog Nrz in the developing zebrafish. Nrz was found to be localized to the yolk syncytial layer, a region containing numerous mitochondria and ER membranes. Nrz knockdown resulted in developmental arrest before gastrulation, due to free Ca(2+) increase in the yolk cell, activating myosin light chain kinase, which led to premature contraction of actin-myosin cables in the margin and separation of the blastomeres from the yolk cell. In the yolk syncytial layer, Nrz appears to prevent the release of Ca(2+) from the endoplasmic reticulum by directly interacting with the IP3R1 Ca(2+) channel. Thus, the Bcl-2 family may participate in early development, not only by controlling apoptosis but also by acting on cytoskeletal dynamics and cell movements via Ca(2+) fluxes inside the embryo.

摘要

Bcl-2 家族成员是细胞凋亡的关键调节因子。它们在其他细胞过程中的作用迄今为止一直被忽视。我们研究了 Bcl-2 同源物 Nrz 在发育中的斑马鱼中的作用。发现 Nrz 定位于卵黄合胞层,该区域含有许多线粒体和内质网膜。由于卵黄细胞中游离 Ca(2+)增加,激活肌球蛋白轻链激酶,导致边缘处的肌动球蛋白电缆过早收缩,卵黄细胞与胚裂球分离,导致 Nrz 敲低导致原肠胚形成前的发育停滞。在卵黄合胞层中,Nrz 似乎通过直接与 IP3R1 Ca(2+)通道相互作用来防止内质网释放 Ca(2+)。因此,Bcl-2 家族可能不仅通过控制细胞凋亡,而且还通过通过胚胎内的 Ca(2+)通量作用于细胞骨架动力学和细胞运动,参与早期发育。

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