Institute of Animal Sciences, University of Agriculture, Faisalabad, Pakistan.
Department of Animal Sciences, University of Illinois at Urbana-Champaign, 1207 West Gregory Drive, Urbana, IL, USA.
Biol Reprod. 2017 Feb 1;96(2):352-365. doi: 10.1095/biolreprod.116.143735.
Formation of complexes between soluble N-ethylmaleimide-sensitive-factor attachment protein receptor (SNARE) proteins on opposing membranes is the minimal requirement for intracellular membrane fusion. The SNARE, syntaxin 2, is found on the sperm plasma membrane and a second SNARE, vesicle associated membrane protein 2 (VAMP2, also known as synaptobrevin 2, SYB2), is on the apposing outer acrosomal membrane. During the acrosome reaction, the outer acrosomal membrane fuses at hundreds of points with the plasma membrane. We hypothesized that syntaxin 2 and VAMP2 redistribute within their respective membranes prior to the acrosome reaction to form trans-SNARE complexes and promote membrane fusion. Immunofluorescence and superresolution structured illumination microscopy were used to localize syntaxin 2 and VAMP2 in mouse sperm during capacitation. Initially, syntaxin 2 was found in puncta throughout the acrosomal region. At 60 and 120 min of capacitation, syntaxin 2 was localized in puncta primarily in the apical ridge. Although deletion of bicarbonate during incubation had no effect, syntaxin 2 puncta were relocated in the restricted region in less than 20% of sperm incubated without albumin. In contrast, VAMP2 was already found in puncta within the apical ridge prior to capacitation. The puncta containing syntaxin 2 and VAMP2 did not precisely co-localize at 0 or 60 min of capacitation time. In summary, syntaxin 2 shifted its location to the apical ridge on the plasma membrane during capacitation in an albumin-dependent manner but VAMP2 was already localized to the apical ridge. Puncta containing VAMP2 did not co-localize with those containing syntaxin 2 during capacitation; therefore, formation of trans-SNARE complexes containing these SNAREs does not occur until after capacitation, immediately prior to acrosomal exocytosis.
可溶性 N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)蛋白在相对膜上形成复合物是细胞内膜融合的最低要求。SNARE 蛋白 syntaxin 2 存在于精子质膜上,另一种 SNARE 蛋白囊泡相关膜蛋白 2(VAMP2,也称为突触融合蛋白 2,SYB2)存在于相对的顶体外膜上。在顶体反应过程中,外顶体膜与质膜融合数百个点。我们假设 syntaxin 2 和 VAMP2 在顶体反应之前在其各自的膜内重新分布,以形成跨 SNARE 复合物并促进膜融合。免疫荧光和超分辨率结构照明显微镜用于在小鼠精子获能过程中定位 syntaxin 2 和 VAMP2。最初,syntaxin 2 发现在顶体区域的整个点。在获能 60 和 120 分钟时,syntaxin 2 主要位于顶端脊的点中定位。尽管在孵育过程中去除碳酸氢盐没有影响,但在没有白蛋白孵育的情况下,不到 20%的精子中 syntaxin 2 点重新定位在限制区域。相比之下,VAMP2 在前顶体脊内的点中在获能之前已经存在。在获能 0 或 60 分钟时,含有 syntaxin 2 和 VAMP2 的点没有精确共定位。总之,syntaxin 2 在白蛋白依赖性方式下向质膜的顶端脊转移其位置,但 VAMP2 已经定位到顶端脊。在获能期间,含有 VAMP2 的点与含有 syntaxin 2 的点不共定位;因此,含有这些 SNARE 的跨 SNARE 复合物的形成直到获能后,即顶体外排之前才发生。