Ovariectomy decreases the mRNA levels of transforming growth factor-beta 1 and increases the mRNA levels of osteocalcin in rat bone in vivo

Biochem Biophys Res Commun. 1993 Aug 16;194(3):1228-33. doi: 10.1006/bbrc.1993.1954.

Abstract

Estrogen depletion causes postmenopausal osteoporosis. Here we report that steady state mRNA levels of transforming growth factor-beta 1 (TGF-beta 1) and osteocalcin in bone persistently decreased and increased, respectively, in vivo in estrogen-depleted rats after ovariectomy (OVX). 21 female Wistar rats (7-month-old) were randomized and underwent OVX or sham-operation, total RNA was extracted from tibiae and assessed by Northern blot analysis. OVX induced 70-80% decrease in TGF-beta 1 mRNA levels and 2- to 3-fold increase in mRNA levels of osteocalcin compared with controls three weeks after surgery. These changes persisted up to twelve weeks post-operation. OVX caused 15% reduction in femoral bone mineral density and 2-fold elevation in serum osteocalcin levels as early as two weeks post-operation. Moreover, estrogen depletion resulted in marked decrease and increase, respectively, in steady state mRNA levels of TGF-beta 1 and osteocalcin in vitro in osteoblastic rat osteosarcoma cells, ROS 17/2.8. Our results provide the first in vivo evidence that expression of TGF-beta and osteocalcin in bone is reciprocally regulated at the transcriptional level in estrogen deficient OVX rats and suggests that TGF-beta 1 may play a role in estrogen-dependent maintenance of normal bone density.

Publication types

  • Comparative Study

MeSH terms

  • Amino Acid Isomerases / biosynthesis
  • Amino Acid Isomerases / genetics
  • Animals
  • Bone Density
  • Bone Resorption / etiology
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics
  • Cells, Cultured
  • Estrogens / deficiency*
  • Female
  • Gene Expression Regulation
  • Osteocalcin / biosynthesis*
  • Osteocalcin / genetics
  • Osteoclasts / metabolism
  • Ovariectomy
  • Peptidylprolyl Isomerase
  • RNA, Messenger / biosynthesis*
  • Rats
  • Rats, Wistar
  • Tibia / metabolism*
  • Time Factors
  • Transforming Growth Factor beta / biosynthesis*
  • Transforming Growth Factor beta / genetics

Substances

  • Carrier Proteins
  • Estrogens
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Osteocalcin
  • Amino Acid Isomerases
  • Peptidylprolyl Isomerase