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顶体胞吐作用,一种特殊类型的受调控分泌。

Acrosomal exocytosis, a special type of regulated secretion.

作者信息

Mayorga Luis S, Tomes Claudia N, Belmonte Silvia A

机构信息

Laboratorio de Biología Celular y Molecular, Instituto de Histología y Embriología (IHEM-CONICET), Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Mendoza, Argentina.

出版信息

IUBMB Life. 2007 Apr-May;59(4-5):286-92. doi: 10.1080/15216540701222872.

Abstract

The acrosome is a single secretory granule present in the head of mammalian--and other animal groups--sperm. Secretion of this granule is an absolute requirement for physiological fertilization. Acrosome exocytosis is a synchronized and tightly regulated all-or-nothing process, with no recycling of membranes. In the last few years, it has been shown that acrosomal exocytosis is mediated by a molecular mechanism that is homologous to that reported in the secretion of neuroendocrinal cells. Moreover, because of its particular characteristics, acrosomal exocytosis is a unique mammalian model for the study of the different steps of the membrane fusion cascade. Combining results in intact and permeabilized sperm, the following sequence of events has been proposed. In resting sperm, SNARE proteins are locked in inactive cis complexes. Sperm activation causes a calcium increase in the cytoplasm that promotes the production of cAMP and activates Rab3A. Afterwards, NSF and alphaSNAP disassemble cis complexes and the free SNAREs are then able to reassemble in loose trans complexes. Membrane fusion is arrested at this stage until calcium is released from inside the acrosome by inositol 1,4,5-trisphosphate-sensitive calcium channels to trigger the final steps of membrane fusion, which require fully assembled trans SNARE complexes and the calcium sensor synaptotagmin. This working model is still incomplete and tentative. Its improvement will be important to share light on this and other processes of regulated exocytosis. Moreover, it will bring new perspectives into the field of sperm-related fertility and sterility.

摘要

顶体是存在于哺乳动物及其他动物类群精子头部的单个分泌颗粒。该颗粒的分泌是生理性受精的绝对必要条件。顶体胞吐作用是一个同步且受到严格调控的全或无过程,不存在膜的再循环。在过去几年中,已表明顶体胞吐作用由一种与神经内分泌细胞分泌中所报道的分子机制同源的分子机制介导。此外,由于其特殊特性,顶体胞吐作用是研究膜融合级联不同步骤的独特哺乳动物模型。结合完整精子和透化精子的研究结果,提出了以下事件序列。在静止精子中,SNARE蛋白被锁定在无活性的顺式复合物中。精子激活导致细胞质中钙增加,促进cAMP的产生并激活Rab3A。随后,NSF和αSNAP拆解顺式复合物,游离的SNAREs随后能够重新组装成松散的反式复合物。膜融合在此阶段被阻断,直到通过肌醇1,4,5 -三磷酸敏感的钙通道从顶体内部释放钙,以触发膜融合的最终步骤,这需要完全组装好的反式SNARE复合物和钙传感器突触结合蛋白。这个工作模型仍然不完整且具有推测性。其改进对于阐明这一过程以及其他受调控的胞吐作用过程将具有重要意义。此外,它将为精子相关的生育和不育领域带来新的视角。

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