Evidence map›Paper›PMID 29279050›Full record

ArticleBiological research2017

Expression regulation and functional analysis of RGS2 and RGS4 in adipogenic and osteogenic differentiation of human mesenchymal stem cells.

Alma Madrigal, Lun Tan, Yuanxiang Zhao

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 21 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

3 authors at 2 institutions in 1 country.

Alma MadrigalBiological Sciences Department, California State Polytechnic University at Pomona, 3801 W. Temple Ave., Pomona, CA, 91768, USA.
Lun TanBiological Sciences Department, California State Polytechnic University at Pomona, 3801 W. Temple Ave., Pomona, CA, 91768, USA.
Yuanxiang ZhaoBiological Sciences Department, California State Polytechnic University at Pomona, 3801 W. Temple Ave., Pomona, CA, 91768, USA. zhao@cpp.edu.ORCID http://orcid.org/0000-0003-1611-4590
California State Polytechnic University · USCity Of Hope National Medical Center · US

Funding

Integration of Research, Mentoring, Role Modeling and Professional Skill-Building to Prepare Students for PhD Programs in Biomedical ResearchR25GM113748 · NIGMS · CALIFORNIA STATE POLY U POMONA · PI ADLER, JILL · 2015 to 2019
$2.4M
Molecular and Cellular Profiling of Human AdipogensisSC3GM116720 · NIGMS · CALIFORNIA STATE POLY U POMONA · PI ZHAO, YUANXIANG · 2016 to 2019
$435k
Adipogenic Toxicity Study of Obesogenic DrugsSC3GM094078 · NIGMS · CALIFORNIA STATE POLY U POMONA · PI ZHAO, YUANXIANG · 2010 to 2013
$416k
National Institutes of Health 1SC3GM094078National Institutes of Health 1SC3GM116720NIGMS NIH HHS R25 GM113748NIGMS NIH HHS SC3 GM094078NIGMS NIH HHS SC3 GM116720
6 · The paper itself

Abstract

backgroundUnderstanding the molecular basis underlying the formation of bone-forming osteocytes and lipid-storing adipocytes will help provide insights into the cause of disorders originating in stem/progenitor cells and develop therapeutic treatments for bone- or adipose-related diseases. In this study, the role of RGS2 and RGS4, two members of the regulators of G protein signaling (RGS) family, was investigated during adipogenenic and osteogenenic differentiation of human mesenchymal stem cells (hMSCs).

resultsExpression of RGS2 and RGS4 were found to be inversely regulated during adipogenesis induced by dexamethasone (DEX) and 3-isobutyl-methylxanthine, regardless if insulin was present, with RGS2 up-regulated and RGS4 down-regulated in response to adipogenic induction. RGS2 expression was also up-regulated during osteogenesis at a level similar to that induced by treatment of DEX alone, a shared component of adipogenic and osteogenic differentiation inducing media, but significantly lower than the level induced by adipogenic inducing media. RGS4 expression was down-regulated during the first 48 h of osteogenesis but up-regulated afterwards, in both cases at levels similar to that induced by DEX alone. Expression knock-down using small interfering RNA against RGS2 resulted in decreased differentiation efficiency during both adipogenesis and osteogenesis. On the other hand, expression knock-down of RGS4 also resulted in decreased adipogenic differentiation but increased osteogenic differentiation.

conclusionsRGS2 and RGS4 are differentially regulated during adipogenic and osteogenic differentiation of hMSCs. In addition, both RGS2 and RGS4 play positive roles during adipogenesis but opposing roles during osteogenesis, with RGS2 as a positive regulator and RGS4 as a negative regulator. These results imply that members of RGS proteins may play multifaceted roles during human adipogenesis and osteogenesis to balance or counterbalance each other's function during those processes.

Indexed as

AdipogenesisGene Expression RegulationHumansMesenchymal Stem CellsOsteocytesOsteogenesisRGS ProteinsTime FactorsRGS4 proteinRGS ProteinsAdipogenesisHuman mesenchymal stem cells (hMSCs)OsteogenesisRGS2RGS4

Identifiers

PMID29279050
PMCPMC5742872
OpenAlexW2778656946

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LicenceCC BY
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Registered trials

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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.