4.5 Article

Effects of Strontium on Collagen Content and Expression of Related Genes in Rat Chondrocytes Cultured In Vitro

Journal

BIOLOGICAL TRACE ELEMENT RESEARCH
Volume 153, Issue 1-3, Pages 212-219

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12011-013-9640-9

Keywords

Strontium; Chondrocyte; MMP-13; Type II collagen; IGF-1

Funding

  1. Program for New Century Excellent Talents in University [NCET-11-0199]
  2. NSFC-Yunnan province [U0836601]
  3. National Key Technology RD Program [2012BAD12B03]
  4. National Natural Science Foundation of China [30600441, 30972212, 30871897, 31072178]
  5. Science Fund for Distinguished Young Scholars of Jilin University [201100009]

Ask authors/readers for more resources

Strontium stimulates cartilage matrix formation in vitro. However, the mechanisms governing these effects have not yet been extensively reported. In this study, chondrocytes were isolated from rat articular cartilage by enzymatic digestion and cultured for 24-72 h with 1-5 mM strontium. We investigated the effects of different concentrations of strontium on collagen content, type II collagen, insulin-like growth factor (IGF-1) and matrix metalloproteinase (MMP)-13 expression in rat cultured articular chondrocytes in vitro. The collagen content of the chondrocytes, determined as hydroxyproline, was measured by a colorimetry method. Type II collagen, IGF-1, and MMP-13 mRNA abundance and protein expression levels were determined by real-time polymerase chain reaction (real-time PCR) and western blot, respectively. The results showed that collagen content from the chondrocytes extracellular matrix increased with increasing strontium concentration. Moreover, 3 and 5 mM strontium strongly stimulated protein expression and mRNA levels of type II collagen and IGF-1. Conversely, MMP-13 expression in chondrocytes decreased dose-dependently with increasing strontium concentration. These results should provide insight into the ability of strontium to promote chondrocyte extracellular matrix synthesis. Strontium could promote collagen synthesis and suppress collagen degradation via the repression of MMP-13 expression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available