APOE Christchurch enhances a disease-associated microglial response to plaque but suppresses response to tau pathology

These findings highlight the ability of the ApoeCh variant to modulate microglial responses based on the type of pathology, enhancing DAM reactivity in amyloid models and dampening neuroinflammation to promote protection in tau models. This suggests that the Christchurch variant's protective effects likely involve multiple mechanisms, including changes in receptor binding and microglial programming.

Authors

Institutions

Publication Details

Journal
Molecular Neurodegeneration
Published
2025-01-22
DOI
https://doi.org/10.1186/s13024-024-00793-x
Citations
11
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
9.26

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

APOE Christchurch enhances a disease-associated microglial response to plaque but suppresses response to tau pathology

Sherilyn Collins, Ángela Gómez-Arboledas, Nellie Kwang, Nicholas T. Seyfried et al.
11 citations
Molecular Neurodegeneration
Neuroinflammation and Neurodegeneration Mechanisms
9.26
article

APOE Christchurch enhances a disease-associated microglial response to plaque but suppresses response to tau pathology

Sherilyn Collins, Ángela Gómez-Arboledas, Nellie Kwang, Nicholas T. Seyfried, Kai‐Xuan Shi, Frank M. LaFerla, Andrea J. Tenner, Zechuan Shi, Kristine M. Tran, Vivek Swarup, Shimako Kawauchi, Duc Minh Duong, Rocio A. Barahona, Kim N. Green, Celia Da Cunha, Grant R. MacGregor, Joshua A. Alcantara, Lindsay A. Hohsfield, Claire A. Butler, Kate I. Tsourmas, Shuling Wang, Cassandra Mar, Donna Chao, Jonathan Neumann, Amber Walker
article en
11 citations

Abstract

These findings highlight the ability of the ApoeCh variant to modulate microglial responses based on the type of pathology, enhancing DAM reactivity in amyloid models and dampening neuroinflammation to promote protection in tau models. This suggests that the Christchurch variant's protective effects likely involve multiple mechanisms, including changes in receptor binding and microglial programming.

Molecular NeurodegenerationVol. 20(1)
Emory University (US), University of California, Irvine (US), Abterra Biosciences (United States) (US)
National Institutes of Health, University of California, Irvine, National Institute on Aging, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 2%
Neuroinflammation and Neurodegeneration Mechanisms
9.26
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.