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鞭毛上的环核苷酸门控通道控制钙离子进入精子。

Cyclic nucleotide-gated channels on the flagellum control Ca2+ entry into sperm.

作者信息

Wiesner B, Weiner J, Middendorff R, Hagen V, Kaupp U B, Weyand I

机构信息

Forschungsinstitut für Molekulare Pharmakologie, D-10315 Berlin.

出版信息

J Cell Biol. 1998 Jul 27;142(2):473-84. doi: 10.1083/jcb.142.2.473.

DOI:10.1083/jcb.142.2.473
PMID:9679145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2133051/
Abstract

Cyclic nucleotide-gated (CNG) channels are key elements of cGMP- and cAMP-signaling pathways in vertebrate photoreceptor cells and in olfactory sensory neurons, respectively. These channels form heterooligomeric complexes composed of at least two distinct subunits (alpha and beta). The alpha subunit of cone photoreceptors is also present in mammalian sperm. Here we identify one short and several long less abundant transcripts of beta subunits in testis. The alpha and beta subunits are expressed in a characteristic temporal and spatial pattern in sperm and precursor cells. In mature sperm, the alpha subunit is observed along the entire flagellum, whereas the short beta subunit is restricted to the principal piece of the flagellum. These findings suggest that different forms of CNG channels coexist in the flagellum. Confocal microscopy in conjunction with the Ca2+ indicator Fluo-3 shows that the CNG channels serve as a Ca2+ entry pathway that responds more sensitively to cGMP than to cAMP. Assuming that CNG channel subtypes differ in their Ca2+ permeability, dissimilar localization of alpha and beta subunits may give rise to a pattern of Ca2+ microdomains along the flagellum, thereby providing the structural basis for control of flagellar bending waves.

摘要

环核苷酸门控(CNG)通道分别是脊椎动物光感受器细胞和嗅觉感觉神经元中cGMP和cAMP信号通路的关键元件。这些通道形成由至少两个不同亚基(α和β)组成的异源寡聚体复合物。视锥光感受器的α亚基也存在于哺乳动物精子中。在这里,我们在睾丸中鉴定出一种短的和几种长的丰度较低的β亚基转录本。α和β亚基在精子和前体细胞中以特征性的时间和空间模式表达。在成熟精子中,α亚基沿整个鞭毛都有观察到,而短的β亚基则局限于鞭毛的主段。这些发现表明不同形式的CNG通道在鞭毛中共存。共聚焦显微镜结合Ca2+指示剂Fluo-3显示,CNG通道作为Ca2+进入途径,对cGMP的反应比对cAMP更敏感。假设CNG通道亚型在Ca2+通透性上存在差异,α和β亚基的不同定位可能会在鞭毛上产生Ca2+微域模式,从而为控制鞭毛弯曲波提供结构基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/cf8f26d0754f/JCB9806033.f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/08ee5951e086/JCB9806033.f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/c2a81be66422/JCB9806033.f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/bf2fe5662166/JCB9806033.f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/5a8f423f0bff/JCB9806033.f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/83cdcc01ba67/JCB9806033.f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/4acae8e7bd43/JCB9806033.f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/b4451b3fe5e7/JCB9806033.f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/29c4cf4d0610/JCB9806033.f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/cf8f26d0754f/JCB9806033.f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/08ee5951e086/JCB9806033.f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/c2a81be66422/JCB9806033.f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/bf2fe5662166/JCB9806033.f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/5a8f423f0bff/JCB9806033.f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/83cdcc01ba67/JCB9806033.f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/4acae8e7bd43/JCB9806033.f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/b4451b3fe5e7/JCB9806033.f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/29c4cf4d0610/JCB9806033.f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/2133051/cf8f26d0754f/JCB9806033.f9.jpg

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