Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota 58201, United States of America.
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota 58201, United States of America.
Neurobiol Dis. 2020 Feb;134:104670. doi: 10.1016/j.nbd.2019.104670. Epub 2019 Nov 9.
Endosomes and lysosomes (endolysosomes) are membrane bounded organelles that play a key role in cell survival and cell death. These acidic intracellular organelles are the principal sites for intracellular hydrolytic activity required for the maintenance of cellular homeostasis. Endolysosomes are involved in the degradation of plasma membrane components, extracellular macromolecules as well as intracellular macromolecules and cellular fragments. Understanding the physiological significance and pathological relevance of endolysosomes is now complicated by relatively recent findings of physical and functional interactions between endolysosomes with other intracellular organelles including endoplasmic reticulum, mitochondria, plasma membranes, and peroxisomes. Indeed, evidence clearly indicates that endolysosome dysfunction and inter-organellar signaling occurs in different neurodegenerative diseases including Alzheimer's disease (AD), HIV-1 associated neurocognitive disease (HAND), Parkinson's disease (PD) as well as various forms of brain cancer such as glioblastoma multiforme (GBM). These findings open new areas of cell biology research focusing on understanding the physiological actions and pathophysiological consequences of inter-organellar communication. Here, we will review findings of others and us that endolysosome de-acidification and dysfunction coupled with impaired inter-organellar signaling is involved in the pathogenesis of AD, HAND, PD, and GBM. A more comprehensive appreciation of cell biology and inter-organellar signaling could lead to the development of new drugs to prevent or cure these diseases.
内体和溶酶体(内溶酶体)是膜结合的细胞器,在细胞存活和细胞死亡中发挥关键作用。这些酸性细胞内细胞器是维持细胞内环境稳定所需的细胞内水解活性的主要部位。内溶酶体参与质膜成分、细胞外大分子以及细胞内大分子和细胞碎片的降解。现在,内溶酶体与其他细胞内细胞器(包括内质网、线粒体、质膜和过氧化物酶体)之间的物理和功能相互作用的相对较新发现,使得对内溶酶体的生理意义和病理相关性的理解变得更加复杂。事实上,有证据清楚地表明,在不同的神经退行性疾病中,包括阿尔茨海默病(AD)、HIV-1 相关神经认知疾病(HAND)、帕金森病(PD)以及各种形式的脑癌,如多形性胶质母细胞瘤(GBM),内溶酶体功能障碍和细胞器间信号传递都会发生。这些发现开辟了细胞生物学研究的新领域,重点研究细胞器间通讯的生理作用和病理生理学后果。在这里,我们将回顾其他人的研究发现,我们自己的研究发现表明,内溶酶体去酸化和功能障碍以及细胞器间信号传递受损与 AD、HAND、PD 和 GBM 的发病机制有关。更全面地了解细胞生物学和细胞器间信号传递可能会导致开发新的药物来预防或治疗这些疾病。