Evidence map›Paper›PMID 37267513›Full record

ArticleBlood2023

Limited plasticity of monocyte fate and function associated with epigenetic scripting at the level of progenitors.

Catherine Rhee, Elizabeth W Scadden, Lai Ping Wong, Giulia Schiroli, Michael C Mazzola, Phillip L Chea, Hiroki Kato, Friedrich F Hoyer, Meeta Mistry, Bum-Kyu Lee and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 9 citations in OpenAlex.

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  10. Ly6CCells · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Catherine RheeCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-1613-1975
Elizabeth W ScaddenCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.
Lai Ping WongDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA.
Giulia SchiroliCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-9812-8728
Michael C MazzolaCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-3000-7997
Phillip L CheaCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.
Hiroki KatoCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-4021-3356
Friedrich F HoyerCenter for Systems Biology, Massachusetts General Hospital, Boston, MA.
Meeta MistryBioinformatics Core, Harvard TH Chan School of Public Health, Boston, MA.ORCID 0000-0002-5830-9479
Bum-Kyu LeeInstitute for Cellular and Molecular Biology, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX.ORCID 0000-0001-7835-419X
Jonghwan KimInstitute for Cellular and Molecular Biology, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX.ORCID 0000-0002-9919-9843
Matthias NahrendorfCenter for Systems Biology, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-4021-1887
Michael K MansourDivision of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0001-8892-8695
David B SykesCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-9788-0221
Ruslan I SadreyevDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA.
David T ScaddenCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0001-9821-7133
Harvard University · USMassachusetts General Hospital · USThe University of Texas at Austin · US

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER P DUGGAN · 1994 to 2026
$31.6M
Transcriptional and epigenetic heterogeneity of stem/progenitor cellsP01HL131477 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI David T Scadden · 2017 to 2026
$24.6M
PROJECT 4: Somatic evolution of the hematopoietic system in cardiovascular diseaseP01HL142494 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Matthias Nahrendorf · 2019 to 2026
$19.5M
The role of spleen tyrosine kinase (syk) in neutrophil responses to pathogenic fungi.R01AI132638 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MANSOUR, MICHAEL K · 2018 to 2021
$1.6M
NHLBI NIH HHS P01 HL131477NHLBI NIH HHS P01 HL142494NIAID NIH HHS R01 AI132638NIDDK NIH HHS P30 DK040561
6 · The paper itself

Abstract

Myeloid cell heterogeneity is known, but whether it is cell-intrinsic or environmentally-directed remains unclear. Here, an inducible/reversible system pausing myeloid differentiation allowed the definition of clone-specific functions that clustered monocytes into subsets with distinctive molecular features. These subsets were orthogonal to the classical/nonclassical categorization and had inherent, restricted characteristics that did not shift under homeostasis, after irradiation, or with infectious stress. Rather, their functional fate was constrained by chromatin accessibility established at or before the granulocyte-monocyte or monocyte-dendritic progenitor level. Subsets of primary monocytes had differential ability to control distinct infectious agents in vivo. Therefore, monocytes are a heterogeneous population of functionally restricted subtypes defined by the epigenome of their progenitors that are differentially selected by physiologic challenges with limited plasticity to transition from one subset to another.

Indexed as

GranulocytesMonocytesCell DifferentiationEpigenesis, GeneticEpigenomeMyeloid Progenitor Cells

Identifiers

PMID37267513
PMCPMC10447620
OpenAlexW4379184776

What OpenQuestion holds

Textmetadata
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.