Walensky L D, Snyder S H
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Cell Biol. 1995 Aug;130(4):857-69. doi: 10.1083/jcb.130.4.857.
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 (IP3R) identified a specific 260 kD band in 1% Triton X-100 extracts of rat, hamster, mouse and dog sperm. In each species, IP3R immunostaining localized to the acrosome cap. Scatchard analysis of [3H]IP3 binding to rat sperm sonicates revealed a curvilinear plot with high affinity (Kd = 26 nM, Bmax = 30 pmol/mg) and low affinity (Kd = 1.6 microM, Bmax = 550 pmol/mg) binding sites, reflecting among the highest receptor densities in mammalian tissue. Immunoelectron microscopy confirmed the acrosomal localization in rat sperm. The IP3R fractionated with acrosomes by discontinuous sucrose gradient centrifugation and was enriched in the medium of acrosome-reacted sperm. ATP-dependent 45Ca2+ loading of digitonin permeabilized rat sperm was decreased by 45% in the presence of 10 microM IP3. The IP3-mediated release of calcium was blocked by heparin. Thapsigargin, a sequiterpene lactone inhibitor of the microsomal Ca(2+)-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 IP3R 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.
钙流是哺乳动物精子顶体反应所必需的,顶体反应是一种由卵子结合引发的胞吐事件,会导致精子细胞内钙含量急剧上升。钙依赖性膜融合导致酶的释放,这些酶在受精过程中促进精子穿透透明带。我们已经对哺乳动物精子中肌醇1,4,5-三磷酸(IP3)门控钙通道和磷酸肌醇信号系统的上游成分进行了表征。肽抗体将Gαq/11和磷脂酶C(PLCβ1)的β1亚型共定位到小鼠精子的顶体前部区域。使用针对纯化的脑IP3受体(IP3R)的多克隆抗体进行的蛋白质印迹分析在大鼠、仓鼠、小鼠和狗精子的1% Triton X-100提取物中鉴定出一条特异性的260 kD条带。在每个物种中,IP3R免疫染色都定位于顶体帽。对[3H]IP3与大鼠精子超声裂解物结合的Scatchard分析显示出一条曲线,具有高亲和力(Kd = 26 nM,Bmax = 30 pmol/mg)和低亲和力(Kd = 1.6 μM,Bmax = 550 pmol/mg)结合位点,这反映了哺乳动物组织中最高的受体密度之一。免疫电子显微镜证实了IP3R在大鼠精子中的顶体定位。通过不连续蔗糖梯度离心,IP3R与顶体一起分级分离,并在顶体反应的精子介质中富集。在10 μM IP3存在的情况下,洋地黄皂苷通透的大鼠精子的ATP依赖性45Ca2+负载量降低了45%。IP3介导的钙释放被肝素阻断。毒胡萝卜素是一种微粒体Ca(2+)-ATPase的倍半萜内酯抑制剂,它刺激小鼠精子顶体反应的程度与Ca2+离子载体A23187相同。咖啡因和ryanodine未能影响钙积累,这表明毒胡萝卜素是通过一个对IP3敏感的储存库起作用的。哺乳动物精子顶体前部区域中存在Gαq/11、PLCβ1和功能性IP3R,以及毒胡萝卜素对顶体反应的诱导,表明IP3门控钙释放参与了哺乳动物的顶体反应。