Priority Research Centre for Reproductive Science, School of Environmental and Life Sciences, Discipline of Biological Sciences, The University of Newcastle, University Drive, Callaghan, NSW, 2308, Australia.
Priority Research Centre for Chemical Biology, School of Environmental and Life Sciences, The University of Newcastle, Callaghan, NSW, 2308, Australia.
BMC Biol. 2019 Apr 18;17(1):35. doi: 10.1186/s12915-019-0653-5.
The mammalian epididymis is responsible for the provision of a highly specialized environment in which spermatozoa acquire functional maturity and are subsequently stored in preparation for ejaculation. Making important contributions to both processes are epididymosomes, small extracellular vesicles released from the epididymal soma via an apocrine secretory pathway. While considerable effort has been focused on defining the cargo transferred between epididymosomes and spermatozoa, comparatively less is known about the mechanistic basis of these interactions. To investigate this phenomenon, we have utilized an in vitro co-culture system to track the transfer of biotinylated protein cargo between mouse epididymosomes and recipient spermatozoa isolated from the caput epididymis; an epididymal segment that is of critical importance for promoting sperm maturation.
Our data indicate that epididymosome-sperm interactions are initiated via tethering of the epididymosome to receptors restricted to the post-acrosomal domain of the sperm head. Thereafter, epididymosomes mediate the transfer of protein cargo to spermatozoa via a process that is dependent on dynamin, a family of mechanoenzymes that direct intercellular vesicle trafficking. Notably, upon co-culture of sperm with epididymosomes, dynamin 1 undergoes a pronounced relocation between the peri- and post-acrosomal domains of the sperm head. This repositioning of dynamin 1 is potentially mediated via its association with membrane rafts and ideally locates the enzyme to facilitate the uptake of epididymosome-borne proteins. Accordingly, disruption of membrane raft integrity or pharmacological inhibition of dynamin both potently suppress the transfer of biotinylated epididymosome proteins to spermatozoa.
Together, these data provide new mechanistic insight into epididymosome-sperm interactions with potential implications extending to the manipulation of sperm maturation for the purpose of fertility regulation.
哺乳动物的附睾负责提供一个高度特化的环境,使精子获得功能成熟,并随后储存起来,为射精做准备。附睾小体是从小体通过顶浆分泌途径释放的小细胞外囊泡,对这两个过程都有重要贡献。虽然人们已经在努力定义附睾小体和精子之间转移的货物,但对于这些相互作用的机制基础了解较少。为了研究这一现象,我们利用体外共培养系统来跟踪生物素化蛋白货物在小鼠附睾小体和从附睾头部分离的受体精子之间的转移;附睾头部对于促进精子成熟至关重要。
我们的数据表明,附睾小体与精子的相互作用是通过将附睾小体与限制在精子头部顶体后区的受体连接而启动的。此后,附睾小体通过一种依赖于动力蛋白的过程将蛋白货物转移到精子中,动力蛋白是一类机械酶,指导细胞间囊泡运输。值得注意的是,在精子与附睾小体共培养时,动力蛋白 1在精子头部的顶体后区和peri-acrosomal 区之间发生明显重定位。这种动力蛋白 1的重定位可能是通过其与膜筏的关联介导的,理想情况下将酶定位到有利于摄取附睾小体携带的蛋白质的位置。因此,破坏膜筏完整性或药理学抑制动力蛋白都能强烈抑制生物素化的附睾小体蛋白向精子的转移。
总之,这些数据为附睾小体与精子的相互作用提供了新的机制见解,这可能对为了控制生育而操纵精子成熟具有重要意义。