Evidence map›Paper›PMID 35411038›Full record

ArticleCell discovery2022

Distinct phases of adult microglia proliferation: a Myc-mediated early phase and a Tnfaip3-mediated late phase.

Wulin Tan, Po-Yi Paul Su, Jacqueline Leff, Xiang Gao, Jiao Chen, Andrew K Guan, Gokul Kalyanasundaram, Averil Ma, Zhonghui Guan

Open access · goldAbstract read
In one paragraph

Article in Cell discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

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  16. Proceedings of the National Academy of Sciences of the United States of America · 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

9 authors at 2 institutions in 2 countries.

Wulin Tan *Department of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Po-Yi Paul Su *Department of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Jacqueline LeffDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Xiang GaoDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Jiao ChenDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Andrew K GuanDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Gokul KalyanasundaramDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA.
Averil MaDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Zhonghui GuanDepartment of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, USA. zhonghui.guan@ucsf.edu.
University of California, San Francisco · USThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

Mechanism of microglia proliferationR01NS121144 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUAN, ZHONGHUI · 2021 to 2025
$2.0M
NINDS NIH HHS R01 NS121144U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS121144
6 · The paper itself

Abstract

Microgliosis is a hallmark of many neurological diseases, including Alzheimer's disease, stroke, seizure, traumatic brain and spinal cord injuries, and peripheral and optic nerve injuries. Recent studies have shown that the newly self-renewed microglia have specific neurological functions. However, the mechanism of adult microglia proliferation remains largely unclear. Here, with single-cell RNA sequencing, flow cytometry, and immunohistochemistry, we demonstrate that the sciatic nerve injury induced two distinct phases of microglia proliferation in mouse spinal cord, each with different gene expression profiles. We demonstrate that the transcription factor Myc was transiently upregulated in spinal cord microglia after nerve injury to mediate an early phase microglia proliferation. On the other hand, we reveal that the tumor-necrosis factor alpha-induced protein 3 (Tnfaip3) was downregulated to mediate the Myc-independent late-phase microglia proliferation. We show that cyclin dependent kinase 1, a kinase with important function in the M phase of the cell cycle, was involved only in the early phase. We reveal that although the early phase was neither necessary nor sufficient for the late phase proliferation, the late-phase suppressed the early phase microglia proliferation in the spinal cord. Finally, we demonstrate that the termination of spinal cord microglia proliferation required both Myc and Tnfaip3 to resume their baseline expression. Thus, we have delineated an interactive signaling network in the proliferation of differentiated microglia.

Identifiers

PMID35411038
PMCPMC9001707
OpenAlexW4223498518

What OpenQuestion holds

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LicenceCC BY
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.