Evidence map›Paper›PMID 19772890›Full record

ArticleExperimental hematology2009

Mesenchymal stem cell-educated macrophages: a novel type of alternatively activated macrophages.

Jaehyup Kim, Peiman Hematti

Open access · greenAbstract read
In one paragraph

Article in Experimental hematology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 396 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
396citing papers in PubMed, 1 pooled it
13.3field-weighted citation impact, top 1% 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

396 citing papers in PubMed, 1 synthesis or guideline pooled it, 769 citations in OpenAlex.

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  20. Bone: A Neglected Endocrine Organ?Journal of clinical medicine · 2024
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336 more citing papers are in PubMed but not listed here.

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.

Jaehyup KimDepartment of Medicine, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53705-2275, USA.
Peiman Hematti
University of Wisconsin–Madison · US

Funding

Embryonic Stem Cell Derived HSC Transplantation in Rhesus Macaque ModelK08HL081076 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI HEMATTI, PEIMAN · 2007 to 2011
$682k
NHLBI NIH HHS HL081076NHLBI NIH HHS K08 HL081076
6 · The paper itself

Abstract

objectiveMesenchymal stem cells (MSCs) are capable of modulating the immune system through interaction with a wide range of immune cells. This study investigates the hypothesis that interaction of MSCs with macrophages could play a significant role in their antiinflammatory/immune modulatory effects. MATERIALS AND

methodsMSCs were derived from bone marrow and monocytes were isolated from peripheral blood of healthy donors. We cultured human monocytes for 7 days without any added cytokines to generate macrophages, and then cocultured them for 3 more days with culture-expanded MSCs. We used cell surface antigen expression and intracellular cytokine expression patterns to study the immunophenotype of macrophages at the end of this coculture period, and phagocytic assays to investigate their functional activity in vitro.

resultsMacrophages cocultured with MSCs consistently showed high-level expression of CD206, a marker of alternatively activated macrophages. Furthermore, these macrophages expressed high levels of interleukin (IL)-10 and low levels of IL-12, as determined by intracellular staining, typical of alternatively activated macrophages. However, macrophages cocultured with MSCs also expressed high levels of IL-6 and low levels of tumor necrosis factor-alpha (TNF-alpha) compared to controls. Functionally, macrophages cocultured with MSCs showed a higher level of phagocytic activity.

conclusionsWe describe a novel type of human macrophage generated in vitro after coculture with MSCs that assumes an immunophenotype defined as IL-10-high, IL-12-low, IL-6-high, and TNF-alpha-low secreting cells. These MSC-educated macrophages may be a unique and novel type of alternatively activated macrophage with a potentially significant role in tissue repair.

Indexed as

Bone Marrow CellsCells, CulturedCoculture TechniquesFlow CytometryHumansImmunophenotypingInterleukin-10Interleukin-12Interleukin-6Lectins, C-TypeMacrophagesMannose-Binding LectinsMannose ReceptorMesenchymal Stem CellsPhagocytesPhagocytosisInterleukin-10Interleukin-12Interleukin-6Lectins, C-TypeMannose-Binding LectinsMannose ReceptorReceptors, Cell SurfaceTumor Necrosis Factor-alpha

Identifiers

PMID19772890
PMCPMC2783735
OpenAlexW2069399162

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.