Evidence map›Paper›PMID 26806720›Full record

ReviewExperimental hematology2016

Macrophages: Key regulators of steady-state and demand-adapted hematopoiesis.

Amanda McCabe, Katherine C MacNamara

Open access · greenAbstract readReview
In one paragraph

Review in Experimental hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 60 citations in OpenAlex.

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  14. The mechanisms of pathological extramedullary hematopoiesis in diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
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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

2 authors at 1 institution in 1 country.

Amanda McCabeCenter for Immunology and Microbial Disease, Albany Medical College, Albany, NY.
Katherine C MacNamaraCenter for Immunology and Microbial Disease, Albany Medical College, Albany, NY. Electronic address: macnamk@mail.amc.edu.
Albany Medical Center Hospital · US

Funding

HSC function during infectionR01GM105949 · NIGMS · ALBANY MEDICAL COLLEGE · PI MACNAMARA, KATHERINE C. · 2014 to 2018
$1.5M
NIGMS NIH HHS R01 GM105949
6 · The paper itself

Abstract

Hematopoietic stem cell (HSC) function is required for balanced blood production throughout life; it is thus essential to understand the mechanisms regulating this highly dynamic process. Bone marrow-resident macrophages (Mϕs) have recently emerged as an important component of the HSC niche, where they contribute to regulating HSC and progenitor cell (HSPC) mobilization and function. Here we review the role of macrophages (Mϕs) on immune cell production, HSPC pool size, and mobilization at steady state and under inflammatory conditions. Inflammation induces marked changes in hematopoiesis to restrict or promote generation of specific cell lineages, and this often has a negative impact on HSC function. Cytokines and growth factors induced during inflammation influence hematopoiesis by acting directly on HSPCs and/or by modulating niche cell function. We focus particular attention on the opposing effects of two key inflammatory proteins, interferon-γ and granulocyte-colony stimulating factor, in regulating bone marrow-resident macrophages (Mϕs) and HSPCs. Macrophages (Mϕs) are essential for tissue homeostasis, and here we highlight their emerging role as a central regulator of both steady-state and demand-adapted hematopoiesis.

Indexed as

HematopoiesisAnimalsBone Marrow CellsCell DifferentiationGranulocyte Colony-Stimulating FactorHematopoietic Stem CellsHumansMacrophagesPhenotypeStress, PhysiologicalGranulocyte Colony-Stimulating Factor

Identifiers

PMID26806720
PMCPMC4852701
OpenAlexW2259628957

What OpenQuestion holds

Textmetadata
LicenceTDM
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.