Transient receptor potential-canonical 3 modulates sperm motility and capacitation-associated protein tyrosine phosphorylation via [Ca2+]i mobilization

被引:7
|
作者
Ru, Yanfei [1 ,2 ]
Zhou, Yuchuan [1 ]
Zhang, Yonglian [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Key Lab Mol Androl, State Key Lab Mol Biol,Inst Biochem & Cell Biol, Shanghai 200031, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100864, Peoples R China
[3] Shanghai Inst Planned Parenthood Res, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
TRPC3; Pyr3; sperm motility; capacitation; Ca2+](i); MOUSE SPERM; ACROSOME REACTION; HUMAN SPERMATOZOA; CALCIUM-CHANNELS; TRPC3; CHANNELS; INHIBITION; STORE; CELL; FERTILIZATION; MITOCHONDRIA;
D O I
10.1093/abbs/gmv025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ca2+ signaling is pivotal for sperm maturation, including the processes of motility, capacitation, and the acrosome reaction. As a Ca2+ conductor, transient receptor potential-canonical 3 (TRPC3) plays an important role in somatic cells. However, the function of TRPC3 in sperm is not well understood. Here, a pharmacological approach was used to investigate the role and mechanism of TPRC3 in sperm function. The TRPC3 antagonist Pyr3 could inhibit sperm motility and accelerate capacitation-associated protein tyrosine phosphorylation in a time- and dose-dependent manner, regardless of the presence or absence of Ca2+ in the incubation medium. Further investigation revealed that sperm [Ca2+](i) fell immediately once Pyr3 was added to Ca2+-free medium, and then gradually increased and returned to baseline levels. Moreover, the [Ca2+](i) levels markedly elevated when sperm were incubated for 30 min in the presence of Pyr3; this change was subsequently accompanied by a significant reduction in sperm mitochondrial membrane potential. This study suggested that TRPC3 can modulate sperm function via mobilization of sperm [Ca2+](i).
引用
收藏
页码:404 / 413
页数:10
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