Evidence map›Paper›PMID 33661886›Full record

ArticlePLoS biology2021

CD74 is a regulator of hematopoietic stem cell maintenance.

Shirly Becker-Herman, Milena Rozenberg, Carmit Hillel-Karniel, Naama Gil-Yarom, Mattias P Kramer, Avital Barak, Lital Sever, Keren David, Lihi Radomir, Hadas Lewinsky and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  10. Surfactant Protein-C Regulates Alveolar Type 2 Epithelial Cell Lineages via the CD74 Receptor.Journal of respiratory biology and translational medicine · 2024
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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

15 authors at 3 institutions in 2 countries.

Shirly Becker-HermanDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Milena RozenbergDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Carmit Hillel-KarnielDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Naama Gil-YaromDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Mattias P KramerDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Avital BarakDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Lital SeverDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Keren DavidDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9497-6527
Lihi RadomirDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Hadas LewinskyDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Michal LeviDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9889-9442
Gilgi FriedlanderIlana and Pascal Mantoux Institute for Bioinformatics and Nancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, Israel.
Richard BucalaInternal Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.
Amnon PeledHadassah Hebrew University Hospital, Goldyne Savad Institute of Gene Therapy, Jerusalem, Israel.
Idit ShacharDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-0004-6159
Weizmann Institute of Science · ILHadassah Medical Center · ILYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Hematopoietic stem and progenitor cells (HSPCs) are a small population of undifferentiated cells that have the capacity for self-renewal and differentiate into all blood cell lineages. These cells are the most useful cells for clinical transplantations and for regenerative medicine. So far, it has not been possible to expand adult hematopoietic stem cells (HSCs) without losing their self-renewal properties. CD74 is a cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF), and its mRNA is known to be expressed in HSCs. Here, we demonstrate that mice lacking CD74 exhibit an accumulation of HSCs in the bone marrow (BM) due to their increased potential to repopulate and compete for BM niches. Our results suggest that CD74 regulates the maintenance of the HSCs and CD18 expression. Its absence leads to induced survival of these cells and accumulation of quiescent and proliferating cells. Furthermore, in in vitro experiments, blocking of CD74 elevated the numbers of HSPCs. Thus, we suggest that blocking CD74 could lead to improved clinical insight into BM transplant protocols, enabling improved engraftment.

Indexed as

AdultAnimalsAntigens, Differentiation, B-LymphocyteBone Marrow CellsBone Marrow TransplantationCell LineageFemaleHealthy VolunteersHematopoietic Stem CellsHistocompatibility Antigens Class IIHumansIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMaleMiceMice, Inbred C57BLAntigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IIIntramolecular Oxidoreductasesinvariant chainMacrophage Migration-Inhibitory FactorsMIF protein, human

Identifiers

PMID33661886
PMCPMC7963458
OpenAlexW3135580491

What OpenQuestion holds

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LicenceCC BY
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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.