The overall goal of this research is to understand the sperm function regulation by calcium, cyclic nucleotides and ion channels at the molecular level. This proposal focuses on the roles of a sperm tail ion channel (CatSper1) we discovered. CatSper1 from human and mice is only expressed in testis. The protein in sperm is strikingly localized in the principal piece membrane. Mice deficient in CatSper1 show no gross phenotypes except that males are completely infertile. The cyclic AMP-induced calcium influx into sperm is deficient in CatSper1-null mice. Because of its restricted protein expression in sperm tail and because of its restricted knockout phenotype in male fertility, CatSper1 represents an excellent target for safe non-hormonal male contraceptives.
Aim 1 will determine the physiological roles of CatSper1 in male fertility. CatSper1-deficient males will be examined in detail and the reason(s) for male infertility will be determined.
Aim 2 will uncover the molecular mechanism underlying the CatSper1 function regulation during spermatogenesis and sperm maturation. Four hypotheses will be tested: a. the CatSper1 protein expression is regulated; b. the protein's plasma membrane localization is regulated; c. the protein is modified; and d. the composition of the channel core protein complex is modulated.
Aim 3 will test the current model concerning the roles of the cyclic nucleotide-gated (CNG) ion channels in the sperm cAMP-induced calcium influx.
Aim 4 will test the hypothesis that the CatSper1 channel mediates a """"""""cAMP- calcium positive feedback loop"""""""" in that cAMP causes calcium influx through the channel and the resulting calcium increase, in turn, causes cAMP to rise. Results from this study will allow us to understand the ion mechanism underlying sperm motility and may lay the foundation for the future development of drugs for infertility treatment and for male contraceptives.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD047578-02
Application #
6917066
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Rankin, Tracy L
Project Start
2004-07-01
Project End
2009-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
2
Fiscal Year
2005
Total Cost
$320,963
Indirect Cost
Name
University of Pennsylvania
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Lishko, Polina V; Kirichok, Yuriy; Ren, Dejian et al. (2012) The control of male fertility by spermatozoan ion channels. Annu Rev Physiol 74:453-75
Ren, Dejian (2011) Calcium signaling in sperm: help from prostasomes. Sci Signal 4:pe27
Xia, Jingsheng; Ren, Dejian (2009) The BSA-induced Ca2+ influx during sperm capacitation is CATSPER channel-dependent. Reprod Biol Endocrinol 7:119
Wang, Haikun; Liu, Jin; Cho, Kwang-Hyun et al. (2009) A novel, single, transmembrane protein CATSPERG is associated with CATSPER1 channel protein. Biol Reprod 81:539-44
Xia, Jingsheng; Ren, Dejian (2009) Egg coat proteins activate calcium entry into mouse sperm via CATSPER channels. Biol Reprod 80:1092-8
Xia, Jingsheng; Reigada, David; Mitchell, Claire H et al. (2007) CATSPER channel-mediated Ca2+ entry into mouse sperm triggers a tail-to-head propagation. Biol Reprod 77:551-9