Skeletal diseases caused by mutations that affect collagen structure and function

Int J Biochem Cell Biol. 2013 Aug;45(8):1556-67. doi: 10.1016/j.biocel.2013.05.017. Epub 2013 May 21.

Abstract

Collagens form critical elements of extracellular matrices that provide mechanical strength to skeletal tissues and serve as a binding platform for cells of bone and cartilage. The formation of collagen-rich extracellular matrices is a complex process that involves intracellular and extracellular steps. Mutations in genes that encode individual chains of triple-helical collagens present in bone and cartilage are associated with heritable diseases of skeletal tissues. In addition, mutations in genes encoding proteins involved in the intracellular and extracellular modifications of collagens are also responsible for developing skeletal abnormalities. In this review, we will summarize the pathomechanisms of molecular and cellular consequences of mutations that alter collagen structure and function. Moreover, we will discuss the prospects and limitations of therapeutic approaches to minimize the effects of mutations that affect collagens of skeletal tissues.

Keywords: Bone; Cartilage; Collagen; ER stress; Heritable diseases.

Publication types

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

MeSH terms

  • Animals
  • Bone Diseases / genetics*
  • Bone Diseases / therapy
  • Cartilage / metabolism
  • Cartilage / pathology
  • Collagen / chemistry*
  • Collagen / genetics*
  • Collagen / metabolism
  • Discoidin Domain Receptors
  • Extracellular Matrix / metabolism
  • Humans
  • Mutation / genetics*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptors, Mitogen / genetics

Substances

  • Receptors, Mitogen
  • Collagen
  • Discoidin Domain Receptors
  • Receptor Protein-Tyrosine Kinases