Leung Miguel Ricardo, Ravi Ravi Teja, Gadella Bart M, Zeev-Ben-Mordehai Tzviya
Bijvoet Centre for Biomolecular Research, Utrecht University, Utrecht, Netherlands.
The Division of Structural Biology, Wellcome Centre for Human Genetics, The University of Oxford, Oxford, United Kingdom.
Front Cell Dev Biol. 2021 Dec 10;9:765673. doi: 10.3389/fcell.2021.765673. eCollection 2021.
To become fertilization-competent, mammalian sperm must undergo a complex series of biochemical and morphological changes in the female reproductive tract. These changes, collectively called capacitation, culminate in the exocytosis of the acrosome, a large vesicle overlying the nucleus. Acrosomal exocytosis is not an all-or-nothing event but rather a regulated process in which vesicle cargo disperses gradually. However, the structural mechanisms underlying this controlled release remain undefined. In addition, unlike other exocytotic events, fusing membranes are shed as vesicles; the cell thus loses the entire anterior two-thirds of its plasma membrane and yet remains intact, while the remaining nonvesiculated plasma membrane becomes fusogenic. Precisely how cell integrity is maintained throughout this drastic vesiculation process is unclear, as is how it ultimately leads to the acquisition of fusion competence. Here, we use cryoelectron tomography to visualize these processes in unfixed, unstained, fully hydrated sperm. We show that paracrystalline structures within the acrosome disassemble during capacitation and acrosomal exocytosis, representing a plausible mechanism for gradual dispersal of the acrosomal matrix. We find that the architecture of the sperm head supports an atypical membrane fission-fusion pathway that maintains cell integrity. Finally, we detail how the acrosome reaction transforms both the micron-scale topography and the nanoscale protein landscape of the sperm surface, thus priming the sperm for fertilization.
为了具备受精能力,哺乳动物的精子必须在雌性生殖道内经历一系列复杂的生化和形态变化。这些变化统称为获能,最终导致顶体(覆盖在细胞核上的一个大囊泡)的胞吐作用。顶体胞吐不是一个全或无的事件,而是一个调节过程,其中囊泡内容物逐渐分散。然而,这种控制释放背后的结构机制仍不明确。此外,与其他胞吐事件不同,融合的膜以囊泡的形式脱落;细胞因此失去了其质膜前2/3的全部,但仍保持完整,而剩余的非囊泡化质膜则变得具有融合性。在整个剧烈的囊泡化过程中,细胞完整性究竟是如何维持的尚不清楚,其最终如何导致获得融合能力也不清楚。在这里,我们使用冷冻电子断层扫描技术来观察未固定、未染色、完全水合的精子中的这些过程。我们发现,顶体内的准晶体结构在获能和顶体胞吐过程中会解体,这代表了顶体基质逐渐分散的一种合理机制。我们发现精子头部的结构支持一种非典型的膜裂变-融合途径,该途径可维持细胞完整性。最后,我们详细阐述了顶体反应如何改变精子表面的微米级地形和纳米级蛋白质景观,从而使精子为受精做好准备。