Evidence map›Paper›PMID 21890638›Full record

ArticleThe Journal of biological chemistry2011

Expression patterns and function of chromatin protein HMGB2 during mesenchymal stem cell differentiation.

Noboru Taniguchi, Beatriz Caramés, Emily Hsu, Stephanie Cherqui, Yasuhiko Kawakami, Martin Lotz

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

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  6. Structure and Functions of HMGB2 Protein.International journal of molecular sciences · 2023
    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

6 authors at 2 institutions in 1 country.

Noboru TaniguchiDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037.
Beatriz CaramésDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037.
Emily HsuDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037.
Stephanie CherquiDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037.
Yasuhiko KawakamiStem Cell Institute and Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota 55455.
Martin LotzDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037. Electronic address: mlotz@scripps.edu.
Scripps Research Institute · USUniversity of Minnesota · US

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI FINN, M.G. · 2001 to 2010
$80.3M
TISSUE ACQUISITION, MORPHOLOGY, AND CELL CULTUREP01AG007996 · NIA · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI SAH, ROBERT L · 1989 to 2016
$26.0M
HMGB2 in cartilage homeostasis, aging and osteoarthritisR01AR056026 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI LOTZ, MARTIN K · 2009 to 2013
$2.0M
BD LSR II Special Order SystemS10RR027557 · NCRR · SCRIPPS RESEARCH INSTITUTE, THE · PI POLLARD, KENNETH MICHAEL · 2010 to 2010
$500k
NCRR NIH HHS RR027557NCRR NIH HHS S10 RR027557NIAMS NIH HHS AR056026NIAMS NIH HHS R01 AR056026NIA NIH HHS AG007996NIA NIH HHS P01 AG007996NIGMS NIH HHS GM62116NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

The superficial zone (SZ) of articular cartilage is critical in maintaining tissue function and homeostasis and represents the site of the earliest changes in osteoarthritis (OA). The expression of chromatin protein HMGB2 is restricted to the SZ, which contains cells expressing mesenchymal stem cell (MSC) markers. Age-related loss of HMGB2 and gene deletion are associated with reduced SZ cellularity and early onset OA. This study addressed HMGB2 expression patterns in MSC and its role during differentiation. HMGB2 was detected at higher levels in human MSC as compared with human articular chondrocytes, and its expression declined during chondrogenic differentiation of MSC. Lentiviral HMGB2 transduction of MSC suppressed chondrogenesis as reflected by an inhibition of Col2a1 and Col10a1 expression. Conversely, in bone marrow MSC from Hmgb2(-/-) mice, Col10a1 was more strongly expressed than in wild-type MSC. This is consistent with in vivo results from mouse growth plates showing that Hmgb2 is expressed in proliferating and prehypertrophic zones but not in hypertrophic cartilage where Col10a1 is strongly expressed. Osteogenesis was also accelerated in Hmgb2(-/-) MSC. The expression of Runx2, which plays a major role in late stage chondrocyte differentiation, was enhanced in Hmgb2(-/-) MSC, and HMGB2 negatively regulated the stimulatory effect of Wnt/β-catenin signaling on the Runx2 proximal promoter. These results demonstrate that HMGB2 expression is inversely correlated with the differentiation status of MSC and that HMGB2 suppresses chondrogenic differentiation. The age-related loss of HMGB2 in articular cartilage may represent a mechanism responsible for the decline in adult cartilage stem cell populations.

Indexed as

Adult Stem CellsAnimalsCartilage, ArticularCell DifferentiationChondrocytesChondrogenesisCore Binding Factor Alpha 1 SubunitGene Expression RegulationHMGB2 ProteinHumansMesenchymal Stem CellsMiceMice, KnockoutOsteogenesisPromoter Regions, GeneticWnt Signaling PathwayCore Binding Factor Alpha 1 SubunitHMGB2 ProteinRUNX2 protein, humanRunx2 protein, mouse

Identifiers

PMID21890638
PMCPMC3308860
OpenAlexW1991655436

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.