Constitutive expression of calreticulin in osteoblasts inhibits mineralization

J Cell Biol. 1995 Dec;131(5):1351-9. doi: 10.1083/jcb.131.5.1351.

Abstract

Recent studies have shown that the multifunctional protein calreticulin can localize to the cell nucleus and regulate gene transcription via its ability to bind a protein motif in the DNA-binding domain of nuclear hormone receptors. A number of known modulators of bone cell function, including vitamin D, act through this receptor family, suggesting that calreticulin may regulate their action in bone cells. We have used a gain-of-function strategy to examine this putative role of calreticulin in MC3T3-E1 osteoblastic cells. Purified calreticulin inhibited the binding of the vitamin D receptor to characterized vitamin D response elements in gel retardation assays. This inhibition was due to direct protein-protein interactions between the vitamin D receptor and calreticulin. Expression of calreticulin transcripts declined during MC3T3-E1 osteoblastic differentiation. MC3T3-E1 cells were transfected with calreticulin expression vectors; stably transfected cell lines overexpressing recombinant calreticulin were established and assayed for vitamin D-induced gene expression and the capacity to mineralize. Constitutive calreticulin expression inhibited basal and vitamin D-induced expression of the osteocalcin gene, whereas osteopontin gene expression was unaffected. This pattern mimicked the gene expression pattern observed in parental cells before down-regulation of endogenous calreticulin expression. In long-term cultures of parental or vector-transfected cells, 1 alpha,25-dihydroxyvitamin D3 (1,25[OH]2D3) induced a two- to threefold stimulation of 45Ca accumulation into the matrix layer. Constitutive expression of calreticulin inhibited the 1,25(OH)2D3-induced 45Ca accumulation. This result correlated with the complete absence of mineralization nodules in long-term cultures of calreticulin-transfected cells. These data suggest that calreticulin can regulate bone cell function by interacting with specific nuclear hormone receptor-mediated pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Calcification, Physiologic / physiology*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / physiology*
  • Calreticulin
  • Cell Differentiation
  • Cell Line
  • Gene Expression Regulation
  • Molecular Sequence Data
  • Osteoblasts / physiology*
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteopontin
  • Protein Binding
  • Receptors, Calcitriol / metabolism
  • Receptors, Retinoic Acid / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Retinoid X Receptors
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / physiology*
  • Sialoglycoproteins / genetics
  • Sialoglycoproteins / metabolism
  • Transcription Factors / metabolism
  • Vitamin D-Binding Protein / metabolism

Substances

  • Calcium-Binding Proteins
  • Calreticulin
  • Receptors, Calcitriol
  • Receptors, Retinoic Acid
  • Recombinant Fusion Proteins
  • Retinoid X Receptors
  • Ribonucleoproteins
  • Sialoglycoproteins
  • Transcription Factors
  • Vitamin D-Binding Protein
  • Osteocalcin
  • Osteopontin