The Development of Molecular Biology of Osteoporosis

Int J Mol Sci. 2021 Jul 30;22(15):8182. doi: 10.3390/ijms22158182.

Abstract

Osteoporosis is one of the major bone disorders that affects both women and men, and causes bone deterioration and bone strength. Bone remodeling maintains bone mass and mineral homeostasis through the balanced action of osteoblasts and osteoclasts, which are responsible for bone formation and bone resorption, respectively. The imbalance in bone remodeling is known to be the main cause of osteoporosis. The imbalance can be the result of the action of various molecules produced by one bone cell that acts on other bone cells and influence cell activity. The understanding of the effect of these molecules on bone can help identify new targets and therapeutics to prevent and treat bone disorders. In this article, we have focused on molecules that are produced by osteoblasts, osteocytes, and osteoclasts and their mechanism of action on these cells. We have also summarized the different pharmacological osteoporosis treatments that target different molecular aspects of these bone cells to minimize osteoporosis.

Keywords: bone remodeling; bone therapeutics; osteoblasts; osteoclasts; osteocytes; osteoporosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Density Conservation Agents / pharmacology*
  • Bone Density Conservation Agents / therapeutic use
  • Bone Remodeling
  • Calcium-Regulating Hormones and Agents / pharmacology*
  • Calcium-Regulating Hormones and Agents / therapeutic use
  • Humans
  • Osteoclasts / drug effects
  • Osteoclasts / metabolism
  • Osteoporosis / drug therapy
  • Osteoporosis / metabolism*
  • Osteoporosis / pathology

Substances

  • Bone Density Conservation Agents
  • Calcium-Regulating Hormones and Agents