Evidence map›Paper›PMID 35732333›Full record

ArticleImmunoHorizons2022

RXRα Regulates the Development of Resident Tissue Macrophages.

Jordan Philpott, Simon Kazimierczyk, Parimal Korgaonkar, Evan Bordt, Jaclyn Zois, Chithirachelvi Vasudevan, Di Meng, Ishan Bhatia, Naifang Lu, Brittany Jimena and 3 more

Abstract read
In one paragraph

Article in ImmunoHorizons, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. 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

13 authors.

Jordan PhilpottMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.
Simon KazimierczykMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.
Parimal KorgaonkarCenter for Computational and Integrative Biology, Massachusetts General Hospital, Boston MA.
Evan BordtLurie Center for Autism, Mass General Hospital for Children, Charlestown, MA 02129; and.
Jaclyn ZoisMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.
Chithirachelvi VasudevanMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.ORCID 0000-0002-7520-6930
Di MengMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.
Ishan BhatiaMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.ORCID 0000-0002-9104-3633
Naifang LuCenter for Computational and Integrative Biology, Massachusetts General Hospital, Boston MA.ORCID 0000-0002-8922-8372
Brittany JimenaMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.
Caryn PorterCenter for Computational and Integrative Biology, Massachusetts General Hospital, Boston MA.
Bobby J CherayilMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA.ORCID 0000-0002-6602-3374
Nitya JainMucosal Immunology and Biology Research Center, Mass General Hospital for Children, Charlestown, MA; njain@ccib.mgh.harvard.edu.ORCID 0000-0002-6423-4485

Funding

Cross-talk between iron metabolism and intestinal inflammationR01AI089700 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI CHERAYIL, BOBBY JOSEPH · 2011 to 2020
$4.4M
Maternal Microbial Influences on Early-life Thymic T cell developmentR01AI154626 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, NITYA · 2020 to 2022
$1.5M
Effects of Salmonella infection on bone marrow macrophage progenitorsR21AI155593 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI CHERAYIL, BOBBY JOSEPH · 2021 to 2022
$460k
Deciphering the role of IGF2BP3 in early life T cell developmentR21AI153548 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, NITYA · 2020 to 2021
$455k
NIAID NIH HHS R01 AI089700NIAID NIH HHS R01 AI154626NIAID NIH HHS R21 AI153548NIAID NIH HHS R21 AI155593
6 · The paper itself

Abstract

Resident tissue macrophages (RTMs) develop from distinct waves of embryonic progenitor cells that seed tissues before birth. Tissue-specific signals drive a differentiation program that leads to the functional specialization of RTM subsets. Genetic programs that regulate the development of RTMs are incompletely understood, as are the mechanisms that enable their maintenance in adulthood. In this study, we show that the ligand-activated nuclear hormone receptor, retinoid X receptor (RXR)α, is a key regulator of murine RTM development. Deletion of RXRα in hematopoietic precursors severely curtailed RTM populations in adult tissues, including the spleen, peritoneal cavity, lung, and liver. The deficiency could be traced to the embryonic period, and mice lacking RXRα in hematopoietic lineages had greatly reduced numbers of yolk sac and fetal liver macrophages, a paucity that persisted into the immediate postnatal period.

Indexed as

MacrophagesYolk SacAnimalsCell DifferentiationLiverMiceSpleen

Identifiers

PMID35732333
PMCPMC9316889

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.