Department of Developmental and Molecular Biology, Institute for Aging Studies, Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Proc Natl Acad Sci U S A. 2012 Mar 20;109(12):E705-14. doi: 10.1073/pnas.1113036109. Epub 2012 Feb 13.
Cytosolic proteins can be selectively delivered to lysosomes for degradation through a type of autophagy known as chaperone-mediated autophagy (CMA). CMA contributes to intracellular quality control and to the cellular response to stress. Compromised CMA has been described in aging and in different age-related disorders. CMA substrates cross the lysosomal membrane through a translocation complex; consequently, changes in the properties of the lysosomal membrane should have a marked impact on CMA activity. In this work, we have analyzed the impact that dietary intake of lipids has on CMA activity. We have found that chronic exposure to a high-fat diet or acute exposure to a cholesterol-enriched diet both have an inhibitory effect on CMA. Lysosomes from livers of lipid-challenged mice had a marked decrease in the levels of the CMA receptor, the lysosome-associated membrane protein type 2A, because of loss of its stability at the lysosomal membrane. This accelerated degradation of lysosome-associated membrane protein type 2A, also described as the mechanism that determines the decline in CMA activity with age, results from its increased mobilization to specific lipid regions at the lysosomal membrane. Comparative lipidomic analyses revealed qualitative and quantitative changes in the lipid composition of the lysosomal membrane of the lipid-challenged animals that resemble those observed with age. Our findings identify a previously unknown negative impact of high dietary lipid intake on CMA and underscore the importance of diet composition on CMA malfunction in aging.
细胞质蛋白可以通过一种称为伴侣介导的自噬(CMA)的自噬类型被选择性递送至溶酶体进行降解。CMA 有助于细胞内的质量控制和细胞对压力的反应。在衰老和不同的与年龄相关的疾病中,已经描述了 CMA 的功能受损。CMA 底物通过易位复合物穿过溶酶体膜;因此,溶酶体膜性质的变化应该对 CMA 活性有显著影响。在这项工作中,我们分析了饮食中脂质摄入对 CMA 活性的影响。我们发现,慢性高脂肪饮食或急性富含胆固醇的饮食暴露都会对 CMA 产生抑制作用。由于其在溶酶体膜上的稳定性丧失,脂质挑战小鼠肝脏中的溶酶体的 CMA 受体,即溶酶体相关膜蛋白 2A 水平显著降低。这种溶酶体相关膜蛋白 2A 的加速降解,也被描述为决定 CMA 活性随年龄下降的机制,是由于其在溶酶体膜上特定脂质区域的增加而导致的。比较脂质组学分析显示,脂质挑战动物的溶酶体膜的脂质组成发生了定性和定量变化,类似于与年龄相关的变化。我们的发现确定了高膳食脂质摄入对 CMA 的先前未知的负面影响,并强调了饮食成分对衰老时 CMA 功能障碍的重要性。