Cuervo Ana Maria, Bergamini Ettore, Brunk Ulf T, Dröge Wulf, Ffrench Martine, Terman Alexei
Department of Anatomy and Structural Biology, Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Autophagy. 2005 Oct-Dec;1(3):131-40. doi: 10.4161/auto.1.3.2017. Epub 2005 Oct 13.
A decrease in the turnover of cellular components and the intracellular accumulation of altered macromolecules and organelles are features common to all aged cells. Diminished autophagic activity plays a major role in these age-related manifestations. In this work we review the molecular defects responsible for the malfunctioning of two forms of autophagy, macroautophagy and chaperone-mediated autophagy, in old mammals, and highlight general and cell-type specific consequences of dysfunction of the autophagic system with age. Dietary caloric restriction and antilipolytic agents have been proven to efficiently stimulate autophagy in old rodents. These and other possible experimental restorative efforts are discussed.
细胞成分周转的减少以及改变的大分子和细胞器在细胞内的积累是所有衰老细胞共有的特征。自噬活性降低在这些与衰老相关的表现中起主要作用。在这项工作中,我们回顾了导致老年哺乳动物中两种自噬形式(巨自噬和伴侣介导的自噬)功能失调的分子缺陷,并强调了自噬系统功能随年龄增长而出现的一般和细胞类型特异性后果。饮食热量限制和抗脂解剂已被证明能有效刺激老年啮齿动物的自噬。我们还讨论了这些以及其他可能的实验性恢复措施。