生物
蛋白酵素
组织蛋白酶
溶酶体
细胞生物学
胞浆
细胞凋亡
程序性细胞死亡
细胞器
细胞外
细胞内
自噬
细胞
半胱氨酸蛋白酶
生物化学
酶
作者
Maruša Hafner Česen,Katarina Pegan,Aleš Špes,Boris Turk
标识
DOI:10.1016/j.yexcr.2012.03.005
摘要
Lysosomes are the major cell digestive organelles that were discovered over 50 years ago. They contain a number of hydrolases that help them to degrade intracellular and extracellular material delivered. Among the hydrolases, the cathepsins, a group of proteases enclosed in the lysosomes, have a major role. About a decade ago, the cathepsins were found to participate in apoptosis. Following their release into the cytosol, they cleave Bid and degrade antiapoptotic Bcl-2 proteins, thereby triggering the mitochondrial pathway of apoptosis, with the lysosomal membrane permeabilization being the critical step in this pathway. Lysosomal dysfunction is linked with several diseases, including cancer and neurodegenerative disorders, thereby providing a potential for therapeutic applications. In this review lysosomes and lysosomal proteases involvement in apoptosis and their possible pharmaceutical targeting are discussed.
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