Caveolin-1 in extracellular matrix vesicles secreted from osteoblasts

Bone. 2007 Jul;41(1):52-8. doi: 10.1016/j.bone.2007.02.030. Epub 2007 Mar 14.

Abstract

Caveolin-1 is an essential and signature protein of caveolae, which are small invaginations of the plasma membrane enriched in cholesterol and sphingolipids. Although high levels of expression of caveolin-1 have been demonstrated in osteoblasts as well as endothelial cells, fibroblasts, and muscular cells, the role of caveolin-1 in osteoblasts has not been clarified. Here, we show that caveolin-1 is secreted from osteoblasts in the form of matrix vesicles; extracellular vesicles released from the plasma membrane of osteoblasts. In this study, caveolae and matrix vesicles were similarly enriched in cholesterol and sphingomyelin in fractions isolated from mineralizing MC3T3-E1 cells. Interestingly, in the MC3T3-E1 cells caveolin-1 was enriched in the matrix vesicle fraction as well as the caveolar membrane fraction, and the amount of caveolin-1 in the matrix vesicle fraction increased as differentiation progressed. Localization of caveolin-1 in matrix vesicles was also confirmed in murine tibia. Furthermore, overexpression of caveolin-1 enhanced matrix calcification in MC3T3-E1 cells, whereas knockdown of caveolin-1 diminished it. These results suggest that secreted caveolin-1 as a component of matrix vesicles may play an important role in osteoblast calcification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Alkaline Phosphatase / metabolism
  • Animals
  • Base Sequence
  • Calcification, Physiologic
  • Caveolin 1 / antagonists & inhibitors
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism*
  • Cell Differentiation
  • Cholesterol / metabolism
  • DNA Primers / genetics
  • Extracellular Matrix / metabolism
  • Gene Expression
  • Mice
  • Microscopy, Immunoelectron
  • Osteoblasts / metabolism*
  • Osteoblasts / ultrastructure
  • Phosphates / metabolism
  • RNA Interference
  • Secretory Vesicles / metabolism
  • Sphingomyelins / metabolism
  • Tibia / metabolism
  • Tibia / ultrastructure

Substances

  • Caveolin 1
  • DNA Primers
  • Phosphates
  • Sphingomyelins
  • Cholesterol
  • Alkaline Phosphatase