The role of GRASPs in morphological alterations of Golgi apparatus: mechanisms and effects

被引:11
|
作者
Ji, Guang [1 ,2 ]
Ji, Hui [2 ]
Mo, Xiaoye [1 ]
Li, Ting [1 ]
Yu, Yaduo [3 ]
Hu, Zhiping [1 ]
机构
[1] Cent S Univ, Xiangya Hosp 2, Dept Neurol, Changsha 410011, Hunan, Peoples R China
[2] Hebei Med Univ, Hosp 2, Dept Neurol, Shijiazhuang 050000, Peoples R China
[3] Virginia Commonwealth Univ, Dept Radiat Oncol, Richmond, VA 23298 USA
关键词
Golgi apparatus; GRASP; morphological alteration; neurodegenerative disease; stress; POLO-LIKE KINASE; MATRIX PROTEIN GM130; AMYOTROPHIC-LATERAL-SCLEROSIS; CASPASE-MEDIATED CLEAVAGE; CELL-FREE SYSTEM; ENDOPLASMIC-RETICULUM; MITOTIC PHOSPHORYLATION; REGULATES GOLGI; NEURODEGENERATIVE DISEASES; UNCONVENTIONAL SECRETION;
D O I
10.1515/revneuro-2013-0020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Golgi apparatus (GA) is a pivotal organelle in cell metabolism, functioning not only in the processing and transportation of cargoes but also in ion homeostasis, cell apoptosis, and stress sensing. We are interested in the intricate role of GA and the recently present novel concept of ` GA stress'. GA shows various morphological alterations in many neurodegenerative diseases and cell apoptosis induced by biochemical reagents, mechanisms in which oxidative stress is strongly involved. In turn, the structural changes and morphological alterations of the GA could also transduce stress signals. Therefore, besides the biochemical changes, more attention should be paid to the morphological alterations of the GA itself during pathological processes and diseases. The Golgi reassembly and stacking proteins (GRASPs) have been identified as important components acting in the transformation of Golgi structure, and they may thus affect the Golgi functions and cell behavior. In this review, we will discuss the intricate role of the GRASPs in remodeling the GA morphology and focus on their mechanisms and effects in the processes of Golgi stacking, mitosis, cell apoptosis, and cargo secretion. We would also like to provide a further prospective of their potential biological values in neurodegenerative diseases.
引用
收藏
页码:485 / 497
页数:13
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