Impaired chaperone-mediated autophagy leads to abnormal SORT1 (sortilin 1) turnover and CES1-dependent triglyceride hydrolysis.

You-Jin Choi, Yoon Ah Nam, Ji Ye Hyun, Jihyeon Yu, Yewon Mun, Sung Ho Yun, Wonseok Lee, Cheon Jun Park, Byung Woo Han, Byung-Hoon Lee
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Abstract

SORT1 (sortilin 1), a member of the the Vps10 (vacuolar protein sorting 10) family, is involved in hepatic lipid metabolism by regulating very low-density lipoprotein (VLDL) secretion and facilitating the lysosomal degradation of CES1 (carboxylesterase 1), crucial for triglyceride (TG) breakdown in the liver. This study explores whether SORT1 is targeted for degradation by chaperone-mediated autophagy (CMA), a selective protein degradation pathway that directs proteins containing KFERQ-like motifs to lysosomes via LAMP2A (lysosomal-associated membrane protein 2A). Silencing LAMP2A or HSPA8/Hsc70 with siRNA increased cytosolic SORT1 protein levels. Leupeptin treatment induced lysosomal accumulation of SORT1, unaffected by siLAMP2A co-treatment, indicating CMA-dependent degradation. Human SORT1 contains five KFERQ-like motifs (658VVTKQ662, 730VREVK734, 733VKDLK737, 734KDLKK738, and 735DLKKK739), crucial for HSPA8 recognition; mutating any single amino acid within these motifs decreased HSPA8 binding. Furthermore, compromised CMA activity resulted in elevated SORT1-mediated degradation of CES1, contributing to increased lipid accumulation in hepatocytes. Consistent with in vitro findings, LAMP2A knockdown in mice exacerbated high-fructose diet-induced fatty liver, marked by increased SORT1 and decreased CES1 levels. Conversely, LAMP2A overexpression promoted SORT1 degradation and CES1D accumulation, counteracting fasting-induced CES1D suppression through CMA activation. Our findings reveal that SORT1 is a substrate of CMA, highlighting its crucial role in directing CES1 to lysosomes. Consequently, disrupting CMA-mediated SORT1 degradation significantly affects CES1-dependent TG hydrolysis, thereby affecting hepatic lipid homeostasis.Abbreviations: APOB: apolipoprotein B; CES1: carboxylesterase 1; CMA: chaperone-mediated autophagy; HSPA8/Hsc70: heat shock protein family A (Hsp70) member 8; LAMP2A: lysosomal associated membrane protein 2A; LDL-C: low-density lipoprotein-cholesterol; PLIN: perilipin; SORT1: sortilin 1; TG: triglyceride; VLDL: very low-density lipoprotein; Vps10: vacuolar protein sorting 10.

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伴侣介导的自噬受损导致SORT1 (sortilin 1)的异常转换和ces1依赖性甘油三酯水解。
SORT1 (sortilin 1)是Vps10(液泡蛋白分选10)家族的一员,通过调节极低密度脂蛋白(VLDL)的分泌和促进CES1(羧化酯酶1)的溶酶体降解参与肝脏脂质代谢,CES1(羧化酯酶1)对肝脏甘油三酯(TG)的分解至关重要。本研究探讨了SORT1是否会被伴侣介导的自噬(CMA)降解,CMA是一种选择性的蛋白质降解途径,通过LAMP2A(溶酶体相关膜蛋白2A)将含有kferq样基序的蛋白质引导到溶酶体。用siRNA沉默LAMP2A或HSPA8/Hsc70增加细胞质SORT1蛋白水平。leeptin处理诱导SORT1溶酶体积累,不受siLAMP2A共处理的影响,表明cma依赖性降解。人类SORT1包含5个kferq样基元(658VVTKQ662、730VREVK734、733VKDLK737、734KDLKK738和735DLKKK739),对HSPA8识别至关重要;突变这些基序中的任何一个氨基酸都会降低HSPA8的结合。此外,CMA活性受损导致sort1介导的CES1降解升高,导致肝细胞脂质积累增加。与体外研究结果一致,小鼠中LAMP2A敲低加剧了高果糖饮食诱导的脂肪肝,其特征是SORT1升高,CES1水平降低。相反,LAMP2A过表达促进SORT1降解和CES1D积累,通过CMA激活抵消禁食诱导的CES1D抑制。我们的研究结果表明SORT1是CMA的底物,突出了其在将CES1引导到溶酶体中的关键作用。因此,破坏cma介导的SORT1降解会显著影响ces1依赖性TG水解,从而影响肝脏脂质稳态。
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