Contrasting skeletal phenotypes in mice with an identical mutation targeted to thyroid hormone receptor alpha1 or beta

Mol Endocrinol. 2005 Dec;19(12):3045-59. doi: 10.1210/me.2005-0224. Epub 2005 Jul 28.

Abstract

Thyroid hormone (T(3)) regulates bone turnover and mineralization in adults and is essential for skeletal development. Surprisingly, we identified a phenotype of skeletal thyrotoxicosis in T(3) receptor beta(PV) (TRbeta(PV)) mice in which a targeted frameshift mutation in TRbeta results in resistance to thyroid hormone. To characterize mechanisms underlying thyroid hormone action in bone, we analyzed skeletal development in TRalpha1(PV) mice in which the same PV mutation was targeted to TRalpha1. In contrast to TRbeta(PV) mice, TRalpha1(PV) mutants exhibited skeletal hypothyroidism with delayed endochondral and intramembranous ossification, severe postnatal growth retardation, diminished trabecular bone mineralization, reduced cortical bone deposition, and delayed closure of the skull sutures. Skeletal hypothyroidism in TRalpha1(PV) mutants was accompanied by impaired GH receptor and IGF-I receptor expression and signaling in the growth plate, whereas GH receptor and IGF-I receptor expression and signaling were increased in TRbeta(PV) mice. These data indicate that GH receptor and IGF-I receptor are physiological targets for T(3) action in bone in vivo. The divergent phenotypes observed in TRalpha1(PV) and TRbeta(PV) mice arise because the pituitary gland is a TRbeta-responsive tissue, whereas bone is TRalpha responsive. These studies provide a new understanding of the complex relationship between central and peripheral thyroid status.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Density / genetics
  • Bone Development / genetics*
  • Bone and Bones / chemistry
  • Bone and Bones / cytology
  • Frameshift Mutation
  • Hyperthyroidism / genetics*
  • Hyperthyroidism / metabolism
  • Hypothyroidism / genetics*
  • Hypothyroidism / metabolism
  • Mice
  • Mice, Mutant Strains
  • Osteogenesis / genetics
  • Phenotype
  • Pituitary Gland / metabolism
  • Receptor, IGF Type 1 / genetics
  • Receptor, IGF Type 1 / metabolism
  • Receptors, Somatotropin / genetics
  • Receptors, Somatotropin / metabolism
  • Thyroid Hormone Receptors alpha / analysis
  • Thyroid Hormone Receptors alpha / genetics*
  • Thyroid Hormone Receptors beta / analysis
  • Thyroid Hormone Receptors beta / genetics*
  • Triiodothyronine / metabolism

Substances

  • Receptors, Somatotropin
  • Thyroid Hormone Receptors alpha
  • Thyroid Hormone Receptors beta
  • Triiodothyronine
  • Receptor, IGF Type 1