Differential effects of SORL1 deficiency on the endo-lysosomal network in human neurons and microglia

被引:4
作者
Mishra, Swati [1 ,3 ]
Jayadev, Suman [2 ,3 ]
Young, Jessica E. [1 ,3 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98109 USA
[2] Univ Washington, Dept Neurol, Seattle, WA 98109 USA
[3] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98109 USA
关键词
SORL1; Alzheimer's disease; endosomal trafficking; neurons; microglia; SPORADIC ALZHEIMERS-DISEASE; AMYLOID PRECURSOR PROTEIN; A-BETA; ENDOCYTIC PATHWAY; RETROMER COMPLEX; GENE SORL1; AUTOPHAGY; SYSTEM; RISK; RECEPTOR;
D O I
10.1098/rstb.2022.0389
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The endosomal gene SORL1 is a strong Alzheimer's disease (AD) risk gene that harbours loss-of-function variants causative for developing AD. The SORL1 protein SORL1/SORLA is an endosomal receptor that interacts with the multi-protein sorting complex retromer to traffic various cargo through the endo-lysosomal network (ELN). Impairments in endo-lysosomal trafficking are an early cellular symptom in AD and a novel therapeutic target. However, the cell types of the central nervous system are diverse and use the ELN differently. If this pathway is to be effectively therapeutically targeted, understanding how key molecules in the ELN function in various cell types and how manipulating them affects cell-type specific responses relative to AD is essential. Here, we discuss an example where deficiency of SORL1 expression in a human model leads to stress on early endosomes and recycling endosomes in neurons, but preferentially leads to stress on lysosomes in microglia. The differences observed in these organelles could relate to the unique roles of these cells in the brain as neurons are professional secretory cells and microglia are professional phagocytic cells. Experiments to untangle these differences are fundamental to advancing the understanding of cell biology in AD and elucidating important pathways for therapeutic development. Human-induced pluripotent stem cell models are a valuable platform for such experiments. This article is part of a discussion meeting issue 'Understanding the endo-lysosomal network in neurodegeneration'.
引用
收藏
页数:7
相关论文
共 75 条
[1]   A genetically modified minipig model for Alzheimer's disease with SORL1 haploinsufficiency [J].
Andersen, Olav M. ;
Bogh, Nikolaj ;
Landau, Anne M. ;
Ploen, Gro G. ;
Jensen, Anne Mette G. ;
Monti, Giulia ;
Ulhoi, Benedicte P. ;
Nyengaard, Jens R. ;
Jacobsen, Kirsten R. ;
Jorgensen, Margarita M. ;
Holm, Ida E. ;
Kristensen, Marianne L. ;
Alstrup, Aage Kristian O. ;
Hansen, Esben S. S. ;
Teunissen, Charlotte E. ;
Breidenbach, Laura ;
Droescher, Mathias ;
Liu, Ying ;
Pedersen, Hanne S. ;
Callesen, Henrik ;
Luo, Yonglun ;
Bolund, Lars ;
Brooks, David J. ;
Laustsen, Christoffer ;
Small, Scott A. ;
Mikkelsen, Lars F. ;
Sorensen, Charlotte B. .
CELL REPORTS MEDICINE, 2022, 3 (09)
[2]   Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein [J].
Andersen, OM ;
Reiche, J ;
Schmidt, V ;
Gotthardt, M ;
Spoelgen, R ;
Behlke, J ;
von Arnim, CAF ;
Breiderhoff, T ;
Jansen, P ;
Wu, X ;
Bales, KR ;
Cappai, R ;
Masters, CL ;
Gliemann, J ;
Mufson, EJ ;
Hyman, BT ;
Paul, SM ;
Nykjær, A ;
Willnow, TE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (38) :13461-13466
[3]   Mitochondria, lysosomes, and dysfunction: their meaning in neurodegeneration [J].
Audano, Matteo ;
Schneider, Anja ;
Mitro, Nico .
JOURNAL OF NEUROCHEMISTRY, 2018, 147 (03) :291-309
[4]  
Bellenguez CEA, 2020, medRxiv, V2020, DOI [10.1101/2020.10.0120200659, DOI 10.1101/2020.10.0120200659]
[5]  
Bhattacharyya R, 2022, SCI REP-UK, V12, DOI 10.1038/s41598-022-07372-4
[6]   Intracellular Toll-like Receptors [J].
Blasius, Amanda L. ;
Beutler, Bruce .
IMMUNITY, 2010, 32 (03) :305-315
[7]   Neuroinflammatory paradigms in lysosomal storage diseases [J].
Bosch, Megan E. ;
Kielian, Tammy .
FRONTIERS IN NEUROSCIENCE, 2015, 9
[8]   The P2X7 Receptor in Microglial Cells Modulates the Endolysosomal Axis, Autophagy, and Phagocytosis [J].
Campagno, Keith E. ;
Mitchell, Claire H. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2021, 15
[9]   Endocytic pathway abnormalities precede amyloid β deposition in sporadic Alzheimer's disease and Down syndrome -: Differential effects of APOE genotype and presenilin mutations [J].
Cataldo, AM ;
Peterhoff, CM ;
Troncosco, JC ;
Gomez-Isla, T ;
Hyman, BT ;
Nixon, RA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (01) :277-286
[10]   Aβ localization in abnormal endosomes:: association with earliest Aβ elevations in AD and Down syndrome [J].
Cataldo, AM ;
Petanceska, S ;
Terio, NB ;
Peterhoff, CM ;
Durham, R ;
Mercken, M ;
Mehta, PD ;
Buxbaum, J ;
Haroutunian, V ;
Nixon, RA .
NEUROBIOLOGY OF AGING, 2004, 25 (10) :1263-1272