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细丝蛋白和磷脂酶C-ε是秀丽隐杆线虫受精囊钙信号传导所必需的。

Filamin and Phospholipase C-ε are required for calcium signaling in the Caenorhabditis elegans Spermatheca.

作者信息

Kovacevic Ismar, Cram Erin J

机构信息

Department of Biology; Northeastern University; Boston, MA USA.

出版信息

Worm. 2013 Jul 1;2(3):e25717. doi: 10.4161/worm.25717. Epub 2013 Jul 12.

DOI:10.4161/worm.25717
PMID:24778940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3875652/
Abstract

Mechanical properties of the microenvironment are fundamental in orchestrating normal tissue function, disease progression, and organismal development. Studies of mechanotransduction in cultured cells on artificial substrates have revealed underlying principles, but the in vivo roles of mechanotransduction remain unclear. We recently reported that the Caenorhabditis elegans spermatheca-a myoepithelial tube composed of a cell monolayer-may be mechanosensitive. Live imaging with the genetically encoded calcium indicator GCaMP revealed that oocyte-induced stretching of the spermatheca resulted in calcium oscillations and constriction of the tube. FLN-1/filamin, a mechanosensitive cytoskeletal scaffolding protein, is required to correctly trigger the calcium transients. PLC-1/phospholipase C-epsilon and ITR-1/IP3 receptor are required to produce the calcium transients, and may function downstream of filamin. In addition to providing important insights into the biology of C. elegans, our studies offer a novel and genetically tractable model for studying mechanotransduction in a myoepithelial tissue.

摘要

微环境的力学特性在协调正常组织功能、疾病进展和机体发育方面至关重要。对人工基质上培养细胞的机械转导研究揭示了其潜在原理,但机械转导在体内的作用仍不清楚。我们最近报道,秀丽隐杆线虫的受精囊——一种由单层细胞组成的肌上皮管——可能具有机械敏感性。使用基因编码的钙指示剂GCaMP进行的实时成像显示,卵母细胞诱导的受精囊拉伸导致钙振荡和管腔收缩。FLN-1/细丝蛋白是一种机械敏感的细胞骨架支架蛋白,是正确触发钙瞬变所必需的。PLC-1/磷脂酶C-ε和ITR-1/IP3受体是产生钙瞬变所必需的,可能在细丝蛋白下游发挥作用。除了为秀丽隐杆线虫生物学提供重要见解外,我们的研究还为研究肌上皮组织中的机械转导提供了一个新的且具有遗传易处理性的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303d/3875652/57a5c20ad8e2/worm-2-e25717-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303d/3875652/57a5c20ad8e2/worm-2-e25717-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303d/3875652/57a5c20ad8e2/worm-2-e25717-g1.jpg

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本文引用的文献

1
Filamin and phospholipase C-ε are required for calcium signaling in the Caenorhabditis elegans spermatheca.细丝蛋白和磷脂酶 C-ε 在秀丽隐杆线虫的受精囊钙离子信号转导中是必需的。
PLoS Genet. 2013 May;9(5):e1003510. doi: 10.1371/journal.pgen.1003510. Epub 2013 May 9.
2
Filamins in mechanosensing and signaling.Filamins 在机械感知和信号转导中的作用。
Annu Rev Biophys. 2012;41:227-46. doi: 10.1146/annurev-biophys-050511-102252. Epub 2012 Feb 23.
3
Structural and functional evaluation of C. elegans filamins FLN-1 and FLN-2.秀丽隐杆线虫肌联蛋白 FLN-1 和 FLN-2 的结构与功能评估。
PLoS One. 2011;6(7):e22428. doi: 10.1371/journal.pone.0022428. Epub 2011 Jul 25.
4
FLN-1/filamin is required for maintenance of actin and exit of fertilized oocytes from the spermatheca in C. elegans.FLN-1/filamin 在 C. elegans 中对于肌动蛋白的维持和受精卵从受精囊的排出是必需的。
Dev Biol. 2010 Nov 15;347(2):247-57. doi: 10.1016/j.ydbio.2010.08.005. Epub 2010 Aug 10.
5
Dual activation of phospholipase C-epsilon by Rho and Ras GTPases.Rho和Ras GTP酶对磷脂酶C-ε的双重激活作用。
J Biol Chem. 2008 Oct 31;283(44):29690-8. doi: 10.1074/jbc.M805038200. Epub 2008 Sep 2.
6
Phospholipase C-epsilon regulates epidermal morphogenesis in Caenorhabditis elegans.磷脂酶C-ε调节秀丽隐杆线虫的表皮形态发生。
PLoS Genet. 2008 Mar 28;4(3):e1000043. doi: 10.1371/journal.pgen.1000043.
7
Structural basis of filamin A functions.细丝蛋白A功能的结构基础。
J Cell Biol. 2007 Dec 3;179(5):1011-25. doi: 10.1083/jcb.200707073.
8
Molecular mechanics of filamin's rod domain.细丝蛋白杆状结构域的分子力学
Biophys J. 2008 Feb 1;94(3):1075-83. doi: 10.1529/biophysj.107.118802. Epub 2007 Oct 5.
9
Phospholipase C epsilon: linking second messengers and small GTPases.磷脂酶Cε:连接第二信使和小GTP酶
Trends Cell Biol. 2006 Dec;16(12):640-8. doi: 10.1016/j.tcb.2006.10.007. Epub 2006 Nov 7.
10
FilGAP, a Rho- and ROCK-regulated GAP for Rac binds filamin A to control actin remodelling.FilGAP是一种受Rho和ROCK调节的Rac的GAP,它与细丝蛋白A结合以控制肌动蛋白重塑。
Nat Cell Biol. 2006 Aug;8(8):803-14. doi: 10.1038/ncb1437. Epub 2006 Jul 23.