Evidence map›Paper›PMID 37813836›Full record

ArticleNature communications2023

Polarized microtubule remodeling transforms the morphology of reactive microglia and drives cytokine release.

Max Adrian, Martin Weber, Ming-Chi Tsai, Caspar Glock, Olga I Kahn, Lilian Phu, Tommy K Cheung, William J Meilandt, Christopher M Rose, Casper C Hoogenraad

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
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  6. Article
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  10. Microglial polarization in retinal neovascularization: Friend or foe?Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  11. iScience · 2026
    Article
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  15. Article
  16. Article
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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.

Max AdrianDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA.ORCID 0000-0002-4926-1258
Martin WeberDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA.
Ming-Chi TsaiDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA.ORCID 0000-0002-6216-8672
Caspar GlockDepartment of OMNI Bioinformatics, Genentech Inc., South San Francisco, CA, 94080, USA.
Olga I KahnDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA.
Lilian PhuDepartment of Microchemistry, Proteomics and Lipidomics, South San Francisco, CA, 94080, USA.
Tommy K CheungDepartment of Microchemistry, Proteomics and Lipidomics, South San Francisco, CA, 94080, USA.
William J MeilandtDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA.
Christopher M RoseDepartment of Microchemistry, Proteomics and Lipidomics, South San Francisco, CA, 94080, USA.ORCID 0000-0002-7502-3368
Casper C HoogenraadDepartment of Neuroscience, Genentech, Inc., South San Francisco, CA, 94080, USA. hoogenraad.casper@gene.com.ORCID 0000-0002-2666-0758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglial reactivity is a pathological hallmark in many neurodegenerative diseases. During stimulation, microglia undergo complex morphological changes, including loss of their characteristic ramified morphology, which is routinely used to detect and quantify inflammation in the brain. However, the underlying molecular mechanisms and the relation between microglial morphology and their pathophysiological function are unknown. Here, proteomic profiling of lipopolysaccharide (LPS)-reactive microglia identifies microtubule remodeling pathways as an early factor that drives the morphological change and subsequently controls cytokine responses. We find that LPS-reactive microglia reorganize their microtubules to form a stable and centrosomally-anchored array to facilitate efficient cytokine trafficking and release. We identify cyclin-dependent kinase 1 (Cdk-1) as a critical upstream regulator of microtubule remodeling and morphological change in-vitro and in-situ. Cdk-1 inhibition also rescues tau and amyloid fibril-induced morphology changes. These results demonstrate a critical role for microtubule dynamics and reorganization in microglial reactivity and modulating cytokine-mediated inflammatory responses.

Indexed as

CytokinesMicrogliaLipopolysaccharidesMicrotubulesProteomicsCytokinesLipopolysaccharides

Identifiers

PMID37813836
PMCPMC10562429

What OpenQuestion holds

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Registered trials

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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.