Evidence map›Paper›PMID 33165955›Full record

ArticleJournal of cellular physiology2021

Retinoic acid increases phagocytosis of myelin by macrophages.

Siyu Wu, Lorenzo Romero-Ramírez, Jörg Mey

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  6. Marine drugs · 2023
    Article
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  9. The roles of microglia and astrocytes in myelin phagocytosis in the central nervous system.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Review
  10. 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

3 authors.

Siyu WuLaboratorio Regeneración Neuronal e Inmunidad Innata, Hospital Nacional de Parapléjicos, Toledo, Spain.
Lorenzo Romero-RamírezLaboratorio Regeneración Neuronal e Inmunidad Innata, Hospital Nacional de Parapléjicos, Toledo, Spain.ORCID 0000-0002-8974-6698
Jörg MeyLaboratorio Regeneración Neuronal e Inmunidad Innata, Hospital Nacional de Parapléjicos, Toledo, Spain.ORCID 0000-0002-8919-3149

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic injuries of the central nervous system (CNS) are followed by the accumulation of cellular debris including proteins and lipids from myelinated fiber tracts. Insufficient phagocytic clearance of myelin debris influences the pathological process because it induces inflammation and blocks axonal regeneration. We investigated whether ligands of nuclear receptor families retinoic acid receptors (RARs), retinoid X receptors, peroxisome proliferator-activated receptors, lipid X receptors, and farnesoid X receptors increase myelin phagocytosis by murine bone marrow-derived macrophages and Raw264.7 cells. Using in vitro assays with 3,3'-dioctadecyloxacarbocyanine perchlorate- and pHrodo-labeled myelin we found that the transcriptional activator all-trans retinoic acid (RA)enhanced endocytosis of myelin involving the induction of tissue transglutaminase-2. The RAR-dependent increase of phagocytosis was not associated with changes in gene expression of receptors FcγR1, FcγR2b, FcγR3, TREM2, DAP12, CR3, or MerTK. The combination of RA and myelin exposure significantly reduced the expression of M1 marker genes inducible nitric oxide synthase and interleukin-1β and increased expression of transmembrane proteins CD36 and ABC-A1, which are involved in lipid transport and metabolism. The present results suggest an additional mechanism for therapeutic applications of RA after CNS trauma. It remains to be studied whether endogenous RA-signaling regulates phagocytosis in vivo.

Indexed as

PhagocytosisAnimalsGene Expression RegulationInflammationMacrophagesMaleMiceMice, Inbred C57BLMicrogliaMyelin SheathPhenotypeRAW 264.7 CellsReceptors, Cytoplasmic and NuclearReceptors, Retinoic AcidTretinoinReceptors, Cytoplasmic and NuclearReceptors, Retinoic AcidTretinoinbone marrow-derived macrophagesinflammationmyelin phagocytosisRARRaw264.7 cellsretinoic acidtransglutaminase

Identifiers

PMID33165955
PMCPMC7984038

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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.