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Department of Brain Sciences
Laboratory of Neurodegenerative Diseases and Aging
1. Journal Articles
Dysregulated Plasma Membrane Turnover Underlying Dendritic Pathology in Neurodegenerative Diseases
Chung, Chang Geon
;
Park, Sung Soon
;
Park, Jeong Hyang
;
Lee, Sung Bae
Department of Brain Sciences
Laboratory of Neurodegenerative Diseases and Aging
1. Journal Articles
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Title
Dysregulated Plasma Membrane Turnover Underlying Dendritic Pathology in Neurodegenerative Diseases
DGIST Authors
Chung, Chang Geon
;
Park, Sung Soon
;
Park, Jeong Hyang
;
Lee, Sung Bae
Issued Date
2020-10
Citation
Chung, Chang Geon. (2020-10). Dysregulated Plasma Membrane Turnover Underlying Dendritic Pathology in Neurodegenerative Diseases. doi: 10.3389/fncel.2020.556461
Type
Article
Article Type
Review
Author Keywords
plasma membrane turnover
;
dendritic pathology
;
neurodegenerative diseases
;
Rab GTPases
;
dendritic secretory pathway
;
dendritic endocytic pathway
Keywords
CLATHRIN-COATED VESICLES
;
ER-EXIT SITES
;
ENDOPLASMIC-RETICULUM
;
RAB GTPASES
;
SPINE LOSS
;
SECRETORY TRAFFICKING
;
ENDOSOMAL TRAFFICKING
;
ALZHEIMERS-DISEASE
;
AMPA RECEPTORS
;
MOUSE MODEL
ISSN
1662-5102
Abstract
Due to their enormous surface area compared to other cell types, neurons face unique challenges in properly handling supply and retrieval of the plasma membrane (PM)—a process termed PM turnover—in their distal areas. Because of the length and extensiveness of dendritic branches in neurons, the transport of materials needed for PM turnover from soma to distal dendrites will be inefficient and quite burdensome for somatic organelles. To meet local demands, PM turnover in dendrites most likely requires local cellular machinery, such as dendritic endocytic and secretory systems, dysregulation of which may result in dendritic pathology observed in various neurodegenerative diseases (NDs). Supporting this notion, a growing body of literature provides evidence to suggest the pathogenic contribution of dysregulated PM turnover to dendritic pathology in certain NDs. In this article, we present our perspective view that impaired dendritic endocytic and secretory systems may contribute to dendritic pathology by encumbering PM turnover in NDs. © 2020 Chung, Park, Park and Lee.
URI
http://hdl.handle.net/20.500.11750/12520
DOI
10.3389/fncel.2020.556461
Publisher
Frontiers Media S.A.
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Lee, Sung Bae
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Department of Brain Sciences
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