INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS SELECTIVELY LOCALIZED TO THE ACROSOMES OF MAMMALIAN SPERM

被引:231
|
作者
WALENSKY, LD
SNYDER, SH
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PHARMACOL & MOLEC SCI,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT PSYCHIAT & BEHAV SCI,BALTIMORE,MD 21205
来源
JOURNAL OF CELL BIOLOGY | 1995年 / 130卷 / 04期
关键词
D O I
10.1083/jcb.130.4.857
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Calcium flux is required for the mammalian sperm acrosome reaction, an exocytotic event triggered by egg binding, which results in a dramatic rise in sperm intracellular calcium. Calcium-dependent membrane fusion results in the release of enzymes that facilitate sperm penetration through the zona pellucida during fertilization. We have characterized inositol 1,4,5-trisphosphate (IP3)-gated calcium channels and upstream components of the phosphoinositide signaling system in mammalian sperm. Peptide antibodies colocalized G alpha(q/11) and the beta 1 isoform of phospholipase C (PLC beta 1) to the anterior acrosomal region of mouse sperm. Western blotting using a polyclonal antibody directed against purified brain IP3 receptor (IP(3)R) identified a specific 260 kD band in 1% Triton X-100 extracts of rat, hamster, mouse and dog sperm. In each species, IP(3)R immunostaining localized to the acrosome cap. Scatchard analysis of [H-3]IP3 binding to rat sperm sonicates revealed a curvilinear plot with high affinity (K-d = 26 nM, B-max = 30 pmol/mg) and low affinity (K-d = 1.6 mu M, B-max = 550 pmol/mg) binding sites, reflecting among the highest receptor densities in mammalian tissue. Immunoelectron microscopy confirmed the acrosomal localization in rat sperm. The IP(3)R fractionated with acrosomes by discontinuous sucrose gradient centrifugation and was enriched in the medium of acrosome-reacted sperm. ATP-dependent Ca-45(2+) loading of digitonin permeabilized rat sperm was decreased by 45% in the presence of 10 mu M IP3. The IP3-mediated release of calcium was blocked by heparin. Thapsigargin, a sequi-terpene lactone inhibitor of the microsomal Ca2+- ATPase, stimulated the acrosome reaction of mouse sperm to the same extent as the Ca2+ ionophore, A23187. The failure of caffeine and ryanodine to affect calcium accumulation suggested that thapsigargin acted through an IP3-sensitive store. The presence of G alpha(q/11), PLC beta 1 and a functional IP(3)R in the anterior acrosomal region of mammalian sperm, as well as thapsigargin's induction of the acrosome reaction, implicate IP3-gated calcium release in the mammalian acrosome reaction.
引用
收藏
页码:857 / 869
页数:13
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