自噬
糖酵解
生物
细胞生物学
贝肯1
ULK1
厌氧糖酵解
丝氨酸
激酶
磷酸化
平衡
丙酮酸激酶
生物化学
乳酸脱氢酶
安普克
蛋白激酶A
新陈代谢
酶
细胞凋亡
作者
Weixia Sun,Mengshu Jia,Yingyan Feng,Xiawei Cheng
出处
期刊:Autophagy
[Informa]
日期:2023-08-18
卷期号:19 (12): 3240-3241
被引量:14
标识
DOI:10.1080/15548627.2023.2246356
摘要
Lactate is a glycolysis product that is produced from pyruvate by LDH (lactate dehydrogenase) and plays an important role in physiological and pathological processes. However, whether lactate regulates autophagy is still unknown. We recently reported that LDHA is phosphorylated at serine 196 by ULK1 (unc-51 like kinase 1) under nutrient-deprivation conditions, promoting lactate production. Then, lactate mediates PIK3C3/VPS34 lactylation at lysine 356 and lysine 781 via acyltransferase KAT5/TIP60. PIK3C3/VPS34 lactylation enhances the association of PIK3C3/VPS34 with BECN1 (beclin 1, autophagy related), ATG14 and UVRAG, increases PIK3C3/VPS34 lipid kinase activity, promotes macroautophagy/autophagy and facilitates the endolysosomal degradation pathway. PIK3C3/VPS34 hyperlactylation induces autophagy and plays an essential role in skeletal muscle homeostasis and cancer progression. Overall, this study describes an autophagy regulation mechanism and the integration of two highly conserved life processes: glycolysis and autophagy.
科研通智能强力驱动
Strongly Powered by AbleSci AI