Congenital osteopetrotic mutations as probes of the origin, structure, and function of osteoclasts

Clin Orthop Relat Res. 1984 Oct:(189):239-63.

Abstract

Progress has been made in recent years on the cell biology of the osteoclast and the pathogenesis of congenital osteopetrosis. New information is critically evaluated and summarized with respect to the origin, structure, and function of osteoclasts with special reference to osteopetroses. A broader perspective emerges from which to consider the biology of osteoclasts, the heterogeneities in the osteopetroses, and the value of each in elucidating the other, along with treatment of the disorder.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adult
  • Animals
  • Bone Marrow Transplantation
  • Bone Resorption
  • Carbonic Anhydrases / deficiency
  • Dogs
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Killer Cells, Natural / immunology
  • Macrophages / immunology
  • Male
  • Mice
  • Mice, Mutant Strains
  • Osteoclasts / physiology*
  • Osteoclasts / ultrastructure
  • Osteopetrosis / congenital
  • Osteopetrosis / genetics*
  • Osteopetrosis / immunology
  • Osteopetrosis / therapy
  • Parabiosis
  • Parathyroid Hormone / blood
  • Rabbits
  • Rats
  • Spleen / transplantation

Substances

  • Parathyroid Hormone
  • Carbonic Anhydrases