大鼠中枢神经系统高级糖化终产物受体(RAGE)的核表达和细胞质表达。

Jesús A. Mosquera-Sulbaran, A. Pedreáñez, Yenddy Carrero, Catherina Peña
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摘要

高级糖化终产物受体(RAGE)是一种跨膜蛋白,与细胞表面的配体相互作用后,参与诱导炎症过程和氧化应激。细胞表面的钙化是与配体相互作用的必要条件。本研究旨在利用免疫荧光技术确定 RAGE 在诺马勒大鼠大脑和小脑不同部位的表达情况。研究人员分析了七叶脑皮层(分子层/颗粒层:M/GL;锥体层:PL)和下丘脑,以及小脑的分子层(CML)和颗粒层(CGL)。在大脑皮层和小脑中普遍观察到 RAGE 阳性 nu-clei 细胞。在 M/GL 中,观察到细胞核和细胞质中不同程度阳性的细胞,相邻细胞外间隙中伴有 RAGE 阳性物质,神经垛中也有 RAGE 阳性物质。PL中的锥体神经元出现不同程度的核RAGE阳性物质出芽,细胞核和细胞质也出现不同程度的阳性。下丘脑中有大量细胞核旁和胞质中出现 RAGE 阳性颗粒,但细胞核仍为阴性。在CML中观察到许多阳性细胞核,而在CGL中则很少。这些数据表明,健康大鼠的细胞核和细胞质中储存有 RAGE,并推测在病理情况下这种分子可能会转移到细胞表面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nuclear and cytoplasmic expressions of the receptor for advanced glycation end products (RAGE) in the rat central nervous system.
The receptor for advanced glycation end products (RAGE) is a transmembrane protein involved in the induction of inflammatory processes and oxidative stress after interacting with its ligands on the cell surface. Lo-calization on the cell surface is necessary for interaction with the ligands. This study aimed to determine the expression of RAGE in different parts of the nor-mal rat brain and cerebellum using the immunofluorescence technique. Sev-eralcerebral cortex layers (molecular/granular layers: M/GL; pyramidal layer: PL) and the hypothalamus were analyzed, as well as the molecular layer (CML) and the granular layer (CGL) of the cerebellum. Cells with RAGE-positive nu-clei were generally observed in the brain’s cerebral cortex and cerebellum. In the M/GL, cells with different degrees of positivity in the nucleus and cyto-plasm accompanied by RAGE-positive material in the adjacent extracellular space were observed, and RAGE-positive material in the neuropile. Pyramidal neurons presenting various degrees of nuclear RAGE-positive material budding and cells with different degrees of nuclear and cytoplasmic positivity were ob-served in PL. The hypothalamus showed a high number of cells with RAGE-positive granules adjacent to the nucleus and in the cytoplasm; nuclei remained negative. Many positive nuclei were observed in CML; they were scarce in CGL. These data suggest the storage of RAGE at the nuclear and cytoplasmic levels in healthy rats and hypothesize the possible translocation of this molecule to the cell surface in pathological conditions.
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