Cysteine-rich secretory protein 4 is an inhibitor of transient receptor potential M8 with a role in establishing sperm function

被引:88
作者
Gibbs, Gerard M. [2 ]
Orta, Gerardo [1 ]
Reddy, Thulasimala [2 ]
Koppers, Adam J. [2 ]
Martinez-Lopez, Pablo [1 ]
Luis de la Vega-Beltran, Jose [1 ]
Lo, Jennifer C. Y. [2 ]
Veldhuis, Nicholas [3 ]
Jamsai, Duangporn [2 ,4 ]
McIntyre, Peter [3 ]
Darszon, Alberto [1 ]
O'Bryan, Moira K. [2 ,4 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Genet Desarrollo & Fisiol Mol, Inst Biotecnol, Cuernavaca 62191, Morelos, Mexico
[2] Monash Univ, Dept Anat & Dev Biol, Clayton, Vic 3800, Australia
[3] Monash Univ, Australian Res Council Ctr Excellence Biotechnol, Clayton, Vic 3800, Australia
[4] Univ Melbourne, Dept Pharmacol, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会; 美国国家卫生研究院; 英国医学研究理事会;
关键词
cysteine-rich secretory proteins; antigen; 5; pathogenesis-related; 1; epididymal maturation; fertility; CRISP FAMILY; CYSTEINE-RICH-SECRETORY-PROTEIN-4; CRISP4; EPIDIDYMAL MATURATION; CRYSTAL-STRUCTURE; PROSTATE-CANCER; COLD SENSATION; CA2+ CHANNEL; ION CHANNELS; MOUSE; TRPM8;
D O I
10.1073/pnas.1015935108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cysteine-rich secretory proteins (CRISPs) are a group of four proteins in the mouse that are expressed abundantly in the male reproductive tract, and to a lesser extent in other tissues. Analysis of reptile CRISPs and mouse CRISP2 has shown that CRISPs can regulate cellular homeostasis via ion channels. With the exception of the ability of CRISP2 to regulate ryanodine receptors, the in vivo targets of mammalian CRISPs function are unknown. In this study, we have characterized the ion channel regulatory activity of epididymal CRISP4 using electrophysiology, cell assays, and mouse models. Through patch-clamping of testicular sperm, the CRISP4 CRISP domain was shown to inhibit the transient receptor potential (TRP) ion channel TRPM8. These data were confirmed using a stably transfected CHO cell line. TRPM8 is a major cold receptor in the body, but is found in other tissues, including the testis and on the tail and head of mouse and human sperm. Functional assays using sperm from wild-type mice showed that TRPM8 activation significantly reduced the number of sperm undergoing the progesterone-induced acrosome reaction following capacitation, and that this response was reversed by the coaddition of CRISP4. In accordance, sperm from Crisp4 null mice had a compromised ability to undergo to the progesterone-induced acrosome reaction. Collectively, these data identify CRISP4 as an endogenous regulator of TRPM8 with a role in normal sperm function.
引用
收藏
页码:7034 / 7039
页数:6
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