Evidence map›Paper›PMID 27400795›Full record

ArticleStem cells translational medicine2016

Mesenchymal Stem Cells Modulate the Functional Properties of Microglia via TGF-β Secretion.

Min Young Noh, Su Min Lim, Ki-Wook Oh, Kyung-Ah Cho, Jinseok Park, Kyung-Suk Kim, Su-Jung Lee, Min-Soo Kwon, Seung Hyun Kim

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. miR-214-3p and NCKAP1: A microglial functional dimension of Alzheimer's progression.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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  11. Article
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  14. Csf1Experimental biology and medicine (Maywood, N.J.) · 2025
    Article
  15. Extracellular Vesicles from Mesenchymal Stem Cells Reverse Neuroinflammation and Restore Motor Coordination in Hyperammonemic Rats.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2024
    Article
  16. Article
  17. Article
  18. Review
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10 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

9 authors at 3 institutions in 1 country.

Min Young NohCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Su Min LimCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Ki-Wook OhCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Kyung-Ah ChoCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Jinseok ParkCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Kyung-Suk KimBioengineering Institute, CORESTEM Inc., Seoul, Republic of Korea.
Su-Jung LeeCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Min-Soo KwonDepartment of Pharmacology, School of Medicine, CHA University, Gyeonggi-do, Republic of Korea minsoo100@cha.ac.kr kimsh1@hanyang.ac.kr.
Seung Hyun KimCell Therapy Center and Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea minsoo100@cha.ac.kr kimsh1@hanyang.ac.kr.
Hanyang University · KRCHA University · KRCorestem (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

: The regulation of microglial cell phenotype is a potential therapeutic intervention in neurodegenerative disease. Previously, we reported that transforming growth factor-β (TGF-β) levels in mesenchymal stromal cells (MSCs) could be used as potential biological markers to predict the effectiveness of autologous MSC therapy in patients with amyotrophic lateral sclerosis. However, the underlying mechanism of TGF-β in MSCs was not fully elucidated in determining the functional properties of microglia. In this study, we aimed to clarify the role of TGF-β that is involved in MSC effectiveness, especially focusing on microglia functional properties that play a pivotal role in neuroinflammation. We found that MSC-conditioned media (MSC-CM) inhibited proinflammatory cytokine expression, restored alternative activated microglia phenotype markers (fractalkine receptor, mannose receptor, CD200 receptor), and enhanced phagocytosis in lipopolysaccharide (LPS)-stimulated microglia. In addition, TGF-β in MSC-CM played a major role in these effects by inhibiting the nuclear factor-κB pathway and restoring the TGF-β pathway in LPS-stimulated microglia. Recombinant TGF-β also induced similar effects to MSC-CM in LPS-stimulated microglia. Therefore, we propose that MSCs can modulate the functional properties of microglia via TGF-β secretion, switching them from a classically activated phenotype to an inflammation-resolving phenotype. The latter role may be associated with the inhibition of neuroinflammatory processes in neurodegenerative disorders. SIGNIFICANCE: The results of this study showed that microglia functional properties may be modulated depending on the composition and quantity of mesenchymal stromal cell (MSC)-secreting factors. Transforming growth factor (TGF)-β is proposed as a modulator of microglia functional properties among MSC-secreting factors, and this study aligns with a previous clinical study by these same authors. TGF-β releasing capacity could be an important factor enhancing the therapeutic efficacy of MSCs in clinical trials.

Indexed as

Mesenchymal stem cellsMicrogliaNeurodegenerative diseasesTGF-β

Identifiers

PMID27400795
PMCPMC5070497
OpenAlexW2470262022

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.