Transient receptor potential (TRPC) channels in human sperm:: expression, cellular localization and involvement in the regulation of flagellar motility

被引:99
作者
Castellano, LE
Treviño, CL
Rodríguez, D
Serrano, CJ
Pacheco, J
Tsutsumi, V
Felix, R
Darszon, A [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotechnol, Dept Genet Dev & Mol Physiol, Cuernavaca, Morelos, Mexico
[2] La Salle Univ, Sch Med, Mexico City, DF, Mexico
[3] IPN, CINVESTAV, Dept Expt Pathol, Mexico City 07738, DF, Mexico
[4] IPN, CINVESTAV, Dept Physiol Biophys & Neurosci, Mexico City 07738, DF, Mexico
关键词
Ca(2+) channel; capacitative Ca(2+) entry; transient receptor potential; TRPC; store operated channel; sperm motility;
D O I
10.1016/S0014-5793(03)00305-3
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
Capacitative Ca(2+) entry is a process whereby the activation of Ca(2+) influx through the plasma membrane is triggered by depletion of intracellular Ca(2+) stores. Some transient receptor potential (TRPC) proteins have been proposed as candidates for capacitative Ca(2+) channels. Recent evidence indicates that capacitative Ca(2+) entry participates in the sperm acrosome reaction (AR), an exocytotic process necessary for fertilization. In addition, several TRPCs have been detected heterogeneously distributed in mouse sperm, suggesting that they may participate in other functions such as motility. Using reverse transcription-polymerase chain reaction (RT-PCR) analysis, RNA messengers for TRPC1, 3, 6 and 7 were found in human spermatogenic cells. Confocal indirect immunofluorescence revealed the presence of TRPC1, 3, 4 and 6 differentially localized in the human sperm, and immunogold transmission electron microscopy indicated that TRPC epitopes are mostly associated to the surface of the cells. Because all of them were detected in the flagellum, TRPC channel antagonists were tested in sperm motility using a computer-assisted assay. Our results provide what is to our knowledge the first evidence that these channels may influence human sperm motility. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:69 / 74
页数:6
相关论文
共 26 条
[1]   DO NONSPERMATOZOAL CELLS MAINLY STEM FROM SPERMIOGENESIS - STUDY OF 106 FERTILE AND 102 SUBFERTILE MEN [J].
AUROUX, M ;
COLLIN, C ;
COUVILLERS, ML .
ARCHIVES OF ANDROLOGY, 1985, 14 (01) :73-80
[2]   Ion transport in sperm signaling [J].
Darszon, A ;
Beltrán, C ;
Felix, R ;
Nishigaki, T ;
Treviño, CL .
DEVELOPMENTAL BIOLOGY, 2001, 240 (01) :1-14
[3]   Ni2+ transport by the human Na+/Ca2+ exchanger expressed in Sf9 cells [J].
Egger, M ;
Ruknudin, A ;
Niggli, E ;
Lederer, WJ ;
Schulze, DH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (05) :C1184-C1192
[4]   Human fertilization with round and elongated spermatids [J].
Fishel, S ;
Green, S ;
Hunter, A ;
Lisi, F ;
Rinaldi, L ;
Lisi, R ;
McDermott, H .
HUMAN REPRODUCTION, 1997, 12 (02) :336-340
[5]   Regulation of mRNA stability in mammalian cells [J].
Guhaniyogi, J ;
Brewer, G .
GENE, 2001, 265 (1-2) :11-23
[6]   Inhibition of TRP3 channels by lanthanides -: Block from the cytosolic side of the plasma membrane [J].
Halaszovich, CR ;
Zitt, C ;
Jüngling, E ;
Lückhoff, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37423-37428
[7]   Hyperactivation of mammalian spermatozoa: function and regulation [J].
Ho, HC ;
Suarez, SS .
REPRODUCTION, 2001, 122 (04) :519-526
[8]   An inositol 1,4,5-trisphosphate receptor-gated intracellular Ca2+ store is involved in regulating sperm hyperactivated motility [J].
Ho, HC ;
Suarez, SS .
BIOLOGY OF REPRODUCTION, 2001, 65 (05) :1606-1615
[9]   Identification and localization of T-type voltage-operated calcium channel subunits in human male germ cells - Expression of multiple isoforms [J].
Jagannathan, S ;
Punt, EL ;
Gu, Y ;
Arnoult, C ;
Sakkas, D ;
Barratt, CLR ;
Publicover, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8449-8456
[10]   Lanthanides potentiate TRPC5 currents by an action at extracellular sites close to the pore mouth [J].
Jung, S ;
Mühle, A ;
Schaefer, M ;
Strotmann, R ;
Schultz, G ;
Plant, TD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :3562-3571