Dose-dependent effect of triiodothyronine on the chondrogenic differentiation of mesenchymal stem cells from the bone marrow of female rats

J Pharm Pharmacol. 2018 Jan;70(1):89-100. doi: 10.1111/jphp.12842. Epub 2017 Nov 3.

Abstract

Objectives: Verify the in-vitro effect of triiodothyronine (T3) on the chondrogenic differentiation of female rat bone marrow mesenchymal stem cells (BMMSCs) over several time periods and at several doses.

Methods: CD54 + /CD73 + /CD90 + BMMSCs from Wistar female rats were cultured in chondrogenic medium with or without T3 (0.01; 1; 100; 1000 nm). At seven, 14 and 21 days, the cell morphology, chondrogenic matrix formation and expression of Sox9 and collagen II were evaluated.

Key findings: The dose of 100 nm did not alter the parameters evaluated in any of the periods studied. However, the 0.01 nm T3 dose improved the chondrogenic potential by increasing the chondrogenic matrix formation and expression of Sox9 and collagen II in at least one of the evaluated periods; the 1 nm T3 dose also improved the chondrogenic potential by increasing the chondrogenic matrix formation and the expression of collagen II in at least one of the evaluated periods. The 1000 nm T3 dose improved the chondrogenic potential by increasing the chondrogenic matrix formation and Sox9 expression in at least one of the evaluated periods.

Conclusions: T3 has a dose-dependent effect on the differentiation of BMMSCs from female rats.

Keywords: bone marrow; chondrogenic differentiation; female rats; thyroid hormone.

MeSH terms

  • Animals
  • Cell Differentiation / drug effects*
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrogenesis / drug effects*
  • Collagen Type II / genetics
  • Dose-Response Relationship, Drug
  • Female
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects*
  • Rats
  • Rats, Wistar
  • SOX9 Transcription Factor / genetics
  • Time Factors
  • Triiodothyronine / administration & dosage
  • Triiodothyronine / pharmacology*

Substances

  • Collagen Type II
  • SOX9 Transcription Factor
  • Sox9 protein, rat
  • Triiodothyronine