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乳酸是连接糖酵解和自噬的桥梁,通过乳酰化作用实现。

Lactate is a bridge linking glycolysis and autophagy through lactylation.

机构信息

School of Pharmacy, Optogenetics & Synthetic Biology Interdisciplinary Research Center, State Key Laboratory of Bioreactor Engineering, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, East China University of Science and Technology, Shanghai, China.

出版信息

Autophagy. 2023 Dec;19(12):3240-3241. doi: 10.1080/15548627.2023.2246356. Epub 2023 Aug 18.

Abstract

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.

摘要

乳酸是糖酵解的产物,由 LDH(乳酸脱氢酶)从丙酮酸生成,在生理和病理过程中发挥重要作用。然而,乳酸是否调节自噬尚不清楚。我们最近报道,在营养缺乏条件下,ULK1(UNC-51 样激酶 1)使 LDHA 丝氨酸 196 磷酸化,促进乳酸生成。然后,乳酸通过酰基转移酶 KAT5/TIP60 将 PIK3C3/VPS34 赖氨酸 356 和赖氨酸 781 乳酰化。PIK3C3/VPS34 乳酰化增强了 PIK3C3/VPS34 与 BECN1(自噬相关)、ATG14 和 UVRAG 的结合,增加了 PIK3C3/VPS34 脂质激酶活性,促进巨自噬/自噬,并促进内溶酶体降解途径。PIK3C3/VPS34 过度乳酰化诱导自噬,并在骨骼肌稳态和癌症进展中发挥重要作用。总的来说,这项研究描述了一种自噬调控机制,并整合了两个高度保守的生命过程:糖酵解和自噬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/10621282/4cf22ce28544/KAUP_A_2246356_F0001_C.jpg

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