FC-γ-受体参与的牛胎儿生理信号系统的现代概念

D. M. Masіuk
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引用次数: 0

摘要

本文就牛胎儿空肠细胞Fc-γ受体的表达及循环利用的研究进展作一综述。在此基础上,提出了Fc-γ受体参与的牛胎儿生理信号系统的现代概念。这些结果表明,在整个胎期内,牛肠细胞Fc-γ- r的表达与年龄相关,肠细胞质膜基底外侧和根尖区域具有Fc-γ-结合活性的不同分子量多肽含量的动态变化,并对各组IgG受体具有一定的特征。研究表明,牛胎期空肠肠细胞质膜对fc - γ - r表达的调控受胎儿发育相关机制的调控。所获得的研究结果及其深入分析,使得对FcγR在牛胚胎期的生理功能提出一个科学的概念成为可能。特别是,它们通过母体-胎盘-胎儿链转运信号,是调节肠细胞发育的关键信号系统之一,识别免疫球蛋白和抗原的特异性信号,在羊水中IgG的胞吞和再循环进入胎儿循环中发挥重要作用,并形成胎儿适应宫内功能体的免疫机制,为出生后的抗原压力做好准备。因此,在质膜上表现出Fc-γ结合活性的多肽的表达调控、定位和鉴定,使Fc-γ r参与形成信号系统,控制胎儿的屏障和免疫功能的发育成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modern concept of physiological signaling systems in cattle fetuses with the participation of FC-γ-receptors
The article presents a literature review on the modification of expression and recycling of Fc-γ-receptors of fetal jejunal enterocytes in cattle. Based on the analyzed data, a modern concept of physiological signaling systems in cattle fetuses with the participation of Fc-γ receptors has been developed. These results indicated age-related modulation of FcγR intestinal cells expression during the entire fetal period of cattle, and the dynamics of changes in the content of polypeptides with different molecular weights that exhibit Fc-γ-binding activity in the basolateral and apical regions of the enterocyte’s plasma membrane and have certain characteristic features for each groups of receptors for IgG. It has been proven that the regulation of FcγR expression by plasma membrane of jejunal enterocytes in cattle during the fetal period of ontogenesis is controlled by mechanisms associated with fetal development. The obtained research results and their in-depth analysis made it possible to propose a scientific concept on the physiological functions of FcγR during the fetal period of cattle ontogenesis. In particular, they translocate signals by the mother-placenta-fetus chain, form one of the key signaling systems for regulating the development of enterocytes, recognize specific signals from immunoglobulins and antigens, play an important role in the transcytosis and recycling of IgG from the amniotic fluid into fetal circulation, and form the immune mechanisms of the fetus for the intrauterine functioning body adaptation and prepare it for antigenic pressure after birth. So, the expression modulation, localization and identification of polypeptides on the plasma membrane that exhibit Fc-γ-binding activity, makes it possible to form a signaling system and control the development of barrier and immune functions in the fetus with the participation of FcγR.
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