Level D· Scientific groundwork from lab and animal studiesLaboratory StudyPubMed

The Role of Calcium in Differentiation of Human Adipose-Derived Stem Cells to Adipocytes.

Goudarzi F., Mohammadalipour A., Khodadadi I., Karimi S., Mostoli R., Bahabadi M.

Laboratory Study, published in Mol Biotechnol (2018) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
Mol Biotechnol (2018)
Country
Switzerland
Reported sample size
—
Source database
PubMed
PMID
29488128
DOI
10.1007/s12033-018-0071-x
Citations
22

Abstract (original English)

Differentiation process of mesenchymal stem cells (MSCs) into adipocyte is involved in obesity. Multiple factors such as Ca 2+ play important roles in different stages of this process. Because of the complicated roles of Ca 2+ in adipogenesis, the aim of present investigation was to study the influx and efflux of Ca 2+ into and out of the cells during adipogenesis. Adipose-derived MSCs were used to differentiate into adipocytes. MSCs were exposed to 2.5 mM Ca 2+ or 1.8 mM Ca 2+ plus calcium ionophore, A23187, for 3 days. Lipid staining, triglycerides (TG) content, and glyceraldehyde phosphate dehydrogenase (GAPDH) activity were evaluated to confirm the efficiency of the differentiation. Gene expression of GLUT4, PPARγ2, RAR-α, and calreticulin, as well as the protein levels of GLUT4 and PPARγ2 were determined. Ca 2+ and in particular Ca 2+ plus A23187 significantly lowered the efficiency of differentiation accompanied by decrease in intracellular TG deposits, GAPDH activity and alleviation of gene, and protein levels of GLUT4 and PPARγ2. While calreticulin and RAR-α were remarkably upregulated in A23187 group. This study showed the inhibitory effects of calcium in adipogenesis. Additionally, it indicated the greater inhibitory effect of calreticulin and RAR-α in controlling adipogenesis by higher levels of calcium.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

How we grade evidence
AdipocytesAdipogenesisAdipose TissueCalcimycinCalciumCell DifferentiationCells, CulturedGlyceraldehyde-3-Phosphate DehydrogenasesHumansMesenchymal Stem Cells

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