Evidence map›Paper›PMID 35025109›Full record

ArticleGlia2022

MAC2 is a long-lasting marker of peripheral cell infiltrates into the mouse CNS after bone marrow transplantation and coronavirus infection.

Lindsay A Hohsfield, Kate I Tsourmas, Yasamine Ghorbanian, Amber R Syage, Sung Jin Kim, Yuting Cheng, Susana Furman, Matthew A Inlay, Thomas E Lane, Kim N Green

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 31 citations in OpenAlex.

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  18. Elevated Galectin-3 Is Associated with Aging, Multiple Sclerosis, and Oxidized Phosphatidylcholine-Induced Neurodegeneration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Lindsay A HohsfieldDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Kate I TsourmasDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Yasamine GhorbanianSue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, California, USA.
Amber R SyageDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Sung Jin KimDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Yuting ChengDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Susana FurmanDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.
Matthew A InlaySue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, California, USA.ORCID 0000-0002-0451-2076
Thomas E LaneDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.ORCID 0000-0003-0392-0825
Kim N GreenDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, California, USA.ORCID 0000-0002-6049-6744
University of California, Irvine · US

Funding

UC Irvine MODEL-ADU54AG054349 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Kim Green · 2017 to 2026
$71.9M
Origins, properties, and therapeutic potential of cells that repopulate the microglia-depleted adult brainR01NS083801 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Kim Green · 2014 to 2026
$5.6M
Chemokines and Viral-Induced Neurologic DiseaseR01NS041249 · NINDS · UNIVERSITY OF UTAH · PI LANE, THOMAS E · 2002 to 2019
$5.4M
Defining mechanisms of disease and repair in a viral model of multiple sclerosisR35NS116835 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Thomas E Lane · 2020 to 2026
$5.0M
Training Program in Stem Cell Translational Medicine for Neurological DisordersT32NS082174 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PETER John DONOVAN, Leslie Michels Thompson · 2013 to 2026
$3.3M
Microglia are necessary for cortical plaque formation in Alzheimer's diseaseRF1AG056768 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GREEN, KIM · 2018 to 2018
$2.7M
The lipid amidase NAAA as a therapeutic target for Alzheimer's diseaseRF1AG065329 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GREEN, KIM, PIOMELLI, DANIELE · 2020 to 2020
$2.3M
Viral-induced axonopathy: mechanisms of damage and repairR01NS091939 · NINDS · UNIVERSITY OF UTAH · PI FUJINAMI, ROBERT S, LANE, THOMAS E · 2016 to 2020
$1.7M
Alzheimer's Association AARF-16-442762NIA NIH HHS RF1 AG056768NIA NIH HHS RF1 AG065329NIA NIH HHS U54 AG054349NIH HHS NS082174NINDS NIH HHS R01 NS041249NINDS NIH HHS R01 NS083801NINDS NIH HHS R01 NS091939NINDS NIH HHS R35 NS116835NINDS NIH HHS T32 NS082174
6 · The paper itself

Abstract

Microglia are the primary resident myeloid cells of the brain responsible for maintaining homeostasis and protecting the central nervous system (CNS) from damage and infection. Monocytes and monocyte-derived macrophages arising from the periphery have also been implicated in CNS pathologies, however, distinguishing between different myeloid cell populations in the CNS has been difficult. Here, we set out to develop a reliable histological marker that can assess distinct myeloid cell heterogeneity and functional contributions, particularly in the context of disease and/or neuroinflammation. scRNAseq from brains of mice infected with the neurotropic JHM strain of the mouse hepatitis virus (JHMV), a mouse coronavirus, revealed that Lgals3 is highly upregulated in monocyte and macrophage populations, but not in microglia. Subsequent immunostaining for galectin-3 (encoded by Lgals3), also referred to as MAC2, highlighted the high expression levels of MAC2 protein in infiltrating myeloid cells in JHMV-infected and bone marrow (BM) chimeric mice, in stark contrast to microglia, which expressed little to no staining in these models. Expression of MAC2 was found even 6-10 months following BM-derived cell infiltration into the CNS. We also demonstrate that MAC2 is not a specific label for plaque-associated microglia in the 5xFAD mouse model, but only appears in a distinct subset of these cells in the presence of JHMV infection or during aging. Our data suggest that MAC2 can serve as a reliable and long-lasting histological marker for monocyte/macrophages in the brain, identifying an accessible approach to distinguishing resident microglia from infiltrating cells in the CNS under certain conditions.

Indexed as

Bone Marrow TransplantationCoronavirus InfectionsAnimalsBrainMacrophagesMiceMice, Inbred C57BLMicrogliaAlzheimer's diseasebrainLgals3MAC2microgliamonocytesmouse coronavirus

Identifiers

PMID35025109
PMCPMC8930563
OpenAlexW4206521136

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.