He Yumin, Su Jingyun, Gao Hongrui, Li Jianzhong, Feng Zemeng, Yin Yulong
Animal Nutrition and Human Health Laboratory, College of Life Sciences, Hunan Normal University, Changsha 410081, China.
Hunan Provincial Key Laboratory of Animal Nutritional Physiology and Metabolic Process, Key Laboratory of Agro-Ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, National Engineering Laboratory for Pollution Control and Waste Utilization in Livestock and Poultry Production, Hunan Provincial Engineering Research Canter for Healthy Livestock and Poultry Production, Scientific Observational and Experimental Station of Animal Nutrition and Feed Science in South-Central, Ministry of Agriculture, Changsha 410125, China.
Metabolites. 2022 Aug 12;12(8):740. doi: 10.3390/metabo12080740.
GPRC6A, an important member of the G-protein-coupled receptor superfamily, has been widely studied in body health maintenance and related diseases. However, it is still controversial whether GPRC6A plays a vital role in glucose homeostasis, and the role of GPRC6A on amino acid homeostasis has not been reported. In this study, GPRC6A was knocked out in C57BL6 mice, and we found that GPRC6A plays an important role in the glucose metabolism, mainly affecting the glucose clearance capacity and gluconeogenesis in mice. GPRC6A plays an important role in maintaining amino acid homeostasis under dietary restrictions, and this may be realized by participating in the regulation of autophagy. Since a large amount of amino acid is lost from urine in aged GPRC6A mice, it is possible that GPRC6A regulates amino acid homeostasis by affecting the integrity of tissue structure. GPRC6A is involved in the regulation of mTORC1 activation but is not necessary for mTORC1 activation under sufficient nutritional supply. In the absence of exogenous amino acids, the loss of GPRC6A induces the GCN2 pathway activation and excessive autophagy of cells, leading to the overactivation of mTORC1, which may be detrimental to body health and cell survival. In summary, this study provides a theoretical and experimental basis for the metabolic process of GPRC6A in body growth and health.
GPRC6A是G蛋白偶联受体超家族的重要成员,已在机体健康维持及相关疾病方面得到广泛研究。然而,GPRC6A在葡萄糖稳态中是否发挥关键作用仍存在争议,且GPRC6A在氨基酸稳态方面的作用尚未见报道。在本研究中,我们在C57BL6小鼠中敲除了GPRC6A,发现GPRC6A在葡萄糖代谢中发挥重要作用,主要影响小鼠的葡萄糖清除能力和糖异生。GPRC6A在饮食限制条件下维持氨基酸稳态中起重要作用,这可能是通过参与自噬调节来实现的。由于老年GPRC6A小鼠尿液中大量氨基酸流失,GPRC6A有可能通过影响组织结构完整性来调节氨基酸稳态。GPRC6A参与mTORC1激活的调节,但在营养供应充足时对mTORC1激活并非必需。在缺乏外源性氨基酸时,GPRC6A缺失会诱导GCN2途径激活和细胞过度自噬,导致mTORC1过度激活,这可能对机体健康和细胞存活有害。总之,本研究为GPRC6A在机体生长和健康中的代谢过程提供了理论和实验依据。