Research Center for Molecular Mechanisms of Aging and Age Related Diseases, Moscow Institute of Physics and Technology (National Research University), Dolgoprudny, Russia.
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russia.
J Cell Physiol. 2021 Sep;236(9):6496-6506. doi: 10.1002/jcp.30324. Epub 2021 Feb 11.
The receptor for advanced glycation end products (RAGE) is a signal receptor first shown to be activated by advanced glycation end products, but also by a variety of signal molecules, including pathological advanced oxidation protein products and β-amyloid. However, most of the RAGE activators have multiple intracellular targets, making it difficult to unravel the exact pathway of RAGE activation. Here, we show that the cell-impermeable RAGE fragment sequence (60-76) of the V-domain of the receptor is able to activate RAGE present on the plasma membrane of neurons and, preferentially, astrocytes. This leads to the exocytosis of vesicular glutamate transporter vesicles and the release of glutamate from astrocytes, which stimulate NMDA and AMPA/kainate receptors, resulting in calcium signals predominantly in neurons. Thus, we show a specific mechanism of RAGE activation by the RAGE fragment and propose a mechanism by which RAGE activation can contribute to the neuronal-astrocytic communication in physiology and pathology.
晚期糖基化终产物受体(RAGE)是一种信号受体,最初被证明可被晚期糖基化终产物激活,但也可被多种信号分子激活,包括病理性氧化蛋白产物和β-淀粉样蛋白。然而,大多数 RAGE 激活剂具有多个细胞内靶标,这使得难以阐明 RAGE 激活的确切途径。在这里,我们表明受体 V 结构域的细胞不可渗透的 RAGE 片段序列(60-76)能够激活神经元和优先激活星形胶质细胞上的细胞膜上的 RAGE。这导致囊泡谷氨酸转运体囊泡的胞吐作用和谷氨酸从星形胶质细胞释放,从而刺激 NMDA 和 AMPA/kainate 受体,导致钙信号主要在神经元中。因此,我们展示了 RAGE 片段激活 RAGE 的特定机制,并提出了 RAGE 激活如何有助于生理和病理条件下神经元-星形胶质细胞通讯的机制。