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GIV/Girdin,一种 Gαi/s 的非受体调节剂,调节精子获能过程中的时空信号转导,并且是雄性生育所必需的。

GIV/Girdin, a non-receptor modulator for Gαi/s, regulates spatiotemporal signaling during sperm capacitation and is required for male fertility.

机构信息

Department of Pathology, School of Medicine, University of California San Diego, San Diego, United States.

Department of Cellular and Molecular Medicine, School of Medicine, University of California San Diego, San Diego, United States.

出版信息

Elife. 2021 Aug 19;10:e69160. doi: 10.7554/eLife.69160.

DOI:10.7554/eLife.69160
PMID:34409938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8376251/
Abstract

For a sperm to successfully fertilize an egg, it must first undergo capacitation in the female reproductive tract and later undergo acrosomal reaction (AR) upon encountering an egg surrounded by its vestment. How premature AR is avoided despite rapid surges in signaling cascades during capacitation remains unknown. Using a combination of conditional knockout (cKO) mice and cell-penetrating peptides, we show that GIV (), a guanine nucleotide-exchange modulator (GEM) for trimeric GTPases, is highly expressed in spermatocytes and is required for male fertility. GIV is rapidly phosphoregulated on key tyrosine and serine residues in human and murine spermatozoa. These phosphomodifications enable GIV-GEM to orchestrate two distinct compartmentalized signaling programs in the sperm tail and head; in the tail, GIV enhances PI3K→Akt signals, sperm motility and survival, whereas in the head it inhibits cAMP surge and premature AR. Furthermore, GIV transcripts are downregulated in the testis and semen of infertile men. These findings exemplify the spatiotemporally segregated signaling programs that support sperm capacitation and shed light on a hitherto unforeseen cause of infertility in men.

摘要

为了使精子成功受精卵子,它必须首先在女性生殖道中经历获能,然后在遇到被其外衣包围的卵子时经历顶体反应 (AR)。尽管在获能过程中信号级联迅速增加,但如何避免过早的 AR 仍然未知。我们使用条件性敲除 (cKO) 小鼠和穿透肽的组合,表明 GIV(),一种三聚体 GTP 酶的鸟嘌呤核苷酸交换调节剂 (GEM),在精母细胞中高度表达,并且是雄性生育所必需的。GIV 在人类和鼠精子中的关键酪氨酸和丝氨酸残基上迅速受到磷酸化调节。这些磷酸化修饰使 GIV-GEM 能够在精子尾部和头部协调两个不同的分隔信号程序;在尾部,GIV 增强了 PI3K→Akt 信号、精子运动和存活,而在头部,它抑制了 cAMP 激增和过早的 AR。此外,GIV 转录本在不育男性的睾丸和精液中下调。这些发现体现了支持精子获能的空间和时间分隔的信号程序,并揭示了男性不育的一个迄今尚未预料到的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/a60f93973148/elife-69160-fig8.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/a60f93973148/elife-69160-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/33c13b41d9e8/elife-69160-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/ea7084ea9e5a/elife-69160-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/67c9d919e1d2/elife-69160-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/e2d2f96eac22/elife-69160-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/bd1ea1f5ddb2/elife-69160-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/ea23b7e5ae52/elife-69160-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/6319a2a237dc/elife-69160-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/5601df7fbef8/elife-69160-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/23561030637e/elife-69160-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/d602b135f1c5/elife-69160-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/b23c2647e0a0/elife-69160-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a82/8376251/a60f93973148/elife-69160-fig8.jpg

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