Evidence map›Paper›PMID 32714570›Full record

ArticleCell death discovery2020

Establishment of bone marrow-derived M-CSF receptor-dependent self-renewing macrophages.

Hesham Nasser, Partho Adhikary, Amira Abdel-Daim, Osamu Noyori, Jutatip Panaampon, Ryusho Kariya, Seiji Okada, Wenjuan Ma, Masaya Baba, Hitoshi Takizawa and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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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 at 6 institutions in 3 countries.

Hesham Nasser *Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.
Partho Adhikary *Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.ORCID 0000-0002-3755-0810
Amira Abdel-Daim *Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.ORCID 0000-0002-2151-4233
Osamu NoyoriJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.
Jutatip PanaamponJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.
Ryusho KariyaJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.
Seiji OkadaJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.ORCID 0000-0003-3124-5206
Wenjuan MaInternational Research Center for Medical Sciences, Kumamoto University, Kumamoto, 860-0811 Japan.
Masaya BabaInternational Research Center for Medical Sciences, Kumamoto University, Kumamoto, 860-0811 Japan.
Hitoshi TakizawaInternational Research Center for Medical Sciences, Kumamoto University, Kumamoto, 860-0811 Japan.
Mariko YamaneInstitute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, 860-0811 Japan.
Hitoshi NiwaInstitute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, 860-0811 Japan.
Shinya SuzuJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, 860-0811 Japan.
Kumamoto University · JPKumamoto Health Science University · JPKumamoto Industrial Research Institute · JPRIKEN Center for Biosystems Dynamics Research · JPSuez Canal University · EGUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have revealed that tissue macrophages are derived from yolk sac precursors or fetal liver monocytes, in addition to bone marrow monocytes. The relative contribution of these cells to the tissue macrophage pool is not fully understood, but embryo-derived cells are supposed to be more important because of their capacity to self-renew. Here, we show the presence of adult bone marrow-derived macrophages that retain self-renewing capacity. The self-renewing macrophages were readily obtained by long-term culture of mouse bone marrow cells with macrophage colony-stimulating factor (M-CSF), a key cytokine for macrophage development. They were non-tumorigenic and proliferated in the presence of M-CSF in unlimited numbers. Despite several differences from non-proliferating macrophages, they retained many features of cells of the monocytic lineage, including the differentiation into dendritic cells or osteoclasts. Among the transcription factors involved in the self-renewal of embryonic stem cells, Krüppel-like factor 2 (KLF2) was strongly upregulated upon M-CSF stimulation in the self-renewing macrophages, which was accompanied by the downregulation of MafB, a transcription factor that suppresses KLF2 expression. Indeed, knockdown of KLF2 led to cell cycle arrest and diminished cell proliferation in the self-renewing macrophages. Our new cell model would be useful to unravel differences in phenotype, function, and molecular mechanism of proliferation among self-renewing macrophages with different origins.

Indexed as

Cell growthInnate immune cells

Identifiers

PMID32714570
PMCPMC7378060
OpenAlexW3044497834

What OpenQuestion holds

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LicenceCC BY
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.