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哺乳动物中的支持细胞-生殖细胞通讯网络。

The Sertoli-germ cell communication network in mammals.

作者信息

Jégou B

机构信息

GERM/INSERM CJF 91-04, Campus de Beaulieu, Université de Rennes I, Bretagne, France.

出版信息

Int Rev Cytol. 1993;147:25-96.

PMID:8225836
Abstract

As soon as scientists began to study testicular structure and function, the concept emerged that SCs and GCs communicate. We now know that the seminiferous epithelium is certainly one of the most complex tissues and that the structural and functional supports of SC-GC communication are extremely elaborate. At all stages of sexual maturation, somatic cells and GCs have developed a formidable set of communication devices that are involved in attachment, displacement, cell shaping, and cell-cell transfer of molecules and cellular materials. Some of the best morphologists since the nineteenth century have studied the anatomical basis of the SC-GC dialogue and have laid the foundations to the understanding of the spermatogenic process. Further experimental efforts are still being made. In particular, new data are emerging that have enabled scientists to go beyond the descriptional or deductive aspects and to tackle the mechanical aspects. From the functional point of view, significant progress has been made in deciphering SC-GC cell language. The unique strategic position of the SC allows this cell type to receive, integrate, and emit all the signals required for the spermatogenic process to or from the extratubular compartment (e.g., FSH, testosterone), the peritubular cells (e.g., P-Mod-S), and GCs themselves. Its location also allows it to coordinate GC activity in both the transversal and the longitudinal axes of the seminiferous tubule. The SC barrier and SC products create the physical and chemical microenvironments required for the completion of each of the different steps of spermatogenesis. In addition to the tubule fluid, the SC products directly or indirectly implicated in GC control are proteins, peptides, and steroid(s) involved in germ cell proliferation, differentiation, and metabolism; transport/binding proteins; proteases; extracellular matrix components; energy metabolites; antiproteases; and various membrane components. Sertoli cell polarization results from the existence of SC-SC occluding junctions. The products required for the mitotic phase of spermatogenesis may principally be secreted basally, whereas those required for meiotic division, spermiogenesis, and sperm cells may preferentially be secreted apically. The interaction between SC factors and GCs is mediated by GC membrane receptors and different endocytic processes. The GC secondary pathway(s) involved in SC action remains a mystery. Germ cell markers that would enable a precise assessment of SC influence are lacking. Changes in the composition of the GC complement and in GC size and shape, as well as GC divisions and migration, profoundly affect SC morphology and function.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

一旦科学家们开始研究睾丸的结构和功能,支持细胞(SCs)和生殖细胞(GCs)之间存在交流的概念便应运而生。我们现在知道,生精上皮无疑是最为复杂的组织之一,而支持细胞与生殖细胞间交流的结构和功能支撑极其精细。在性成熟的各个阶段,体细胞和生殖细胞都已形成了一套强大的交流机制,涉及分子和细胞物质的附着、移位、细胞塑形以及细胞间传递。自19世纪以来,一些最优秀的形态学家研究了支持细胞与生殖细胞对话的解剖学基础,为理解生精过程奠定了基础。目前仍在进行进一步的实验研究。特别是,新的数据不断涌现,使科学家们能够超越描述性或推断性层面,着手研究机械方面的问题。从功能角度来看,在解读支持细胞与生殖细胞的细胞语言方面已取得了重大进展。支持细胞独特的战略位置使其能够接收、整合并发出生精过程所需的所有信号,这些信号来自或传向管周间隙(如促卵泡激素、睾酮)、睾丸间质细胞(如P-Mod-S)以及生殖细胞自身。其位置还使其能够在生精小管的横向和纵向轴上协调生殖细胞的活动。支持细胞屏障和支持细胞产物为生精过程各个不同步骤的完成创造了物理和化学微环境。除了小管液外,直接或间接参与生殖细胞调控的支持细胞产物包括参与生殖细胞增殖、分化和代谢的蛋白质、肽和类固醇;转运/结合蛋白;蛋白酶;细胞外基质成分;能量代谢产物;抗蛋白酶以及各种膜成分。支持细胞的极化源于支持细胞间紧密连接的存在。生精有丝分裂期所需的产物可能主要从基底部分泌,而减数分裂、精子形成和精子细胞所需的产物可能优先从顶端分泌。支持细胞因子与生殖细胞之间的相互作用由生殖细胞膜受体和不同的内吞过程介导。参与支持细胞作用的生殖细胞二级信号通路仍是个谜。目前缺乏能够精确评估支持细胞影响的生殖细胞标志物。生殖细胞组成、大小和形状的变化,以及生殖细胞的分裂和迁移,都会深刻影响支持细胞的形态和功能。(摘要截选至400字)

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