Patra Srimanta, Patil Shankargouda, Klionsky Daniel J, Bhutia Sujit K
Cancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Division of Oral Pathology, Department of Maxillofacial Surgery and Diagnostic Sciences, College of Dentistry, Jazan University, Jazan, Saudi Arabia.
J Cell Physiol. 2023 Feb;238(2):287-305. doi: 10.1002/jcp.30928. Epub 2022 Dec 11.
Recent developments in lysosome biology have transformed our view of lysosomes from static garbage disposals that can also act as suicide bags to decidedly dynamic multirole adaptive operators of cellular homeostasis. Lysosome-governed signaling pathways, proteins, and transcription factors equilibrate the rate of catabolism and anabolism (autophagy to lysosomal biogenesis and metabolite pool maintenance) by sensing cellular metabolic status. Lysosomes also interact with other organelles by establishing contact sites through which they exchange cellular contents. Lysosomal function is critically assessed by lysosomal positioning and motility for cellular adaptation. In this setting, mechanistic target of rapamycin kinase (MTOR) is the chief architect of lysosomal signaling to control cellular homeostasis. Notably, lysosomes can orchestrate explicit cell death mechanisms, such as autophagic cell death and lysosomal membrane permeabilization-associated regulated necrotic cell death, to maintain cellular homeostasis. These lines of evidence emphasize that the lysosomes serve as a central signaling hub for cellular homeostasis.
溶酶体生物学的最新进展已经改变了我们对溶酶体的看法,从原本被认为是静态的垃圾处理场所,偶尔也充当“自杀袋”,转变为细胞内稳态中绝对动态的多角色适应性调控者。溶酶体调控的信号通路、蛋白质和转录因子通过感知细胞代谢状态,平衡分解代谢和合成代谢的速率(从自噬到溶酶体生物发生以及代谢物池维持)。溶酶体还通过建立接触位点与其他细胞器相互作用,借此交换细胞内容物。溶酶体的功能通过其定位和运动性进行关键评估,以实现细胞适应。在这种情况下,雷帕霉素激酶(MTOR)的机制靶点是溶酶体信号传导控制细胞内稳态的主要设计者。值得注意的是,溶酶体可以精心安排明确的细胞死亡机制,如自噬性细胞死亡和溶酶体膜通透性相关的程序性坏死性细胞死亡,以维持细胞内稳态。这些证据强调溶酶体是细胞内稳态的核心信号枢纽。