Biology of bone morphogenetic protein in bone repair and regeneration: A role for autologous blood coagulum as carrier

Bone. 2020 Dec:141:115602. doi: 10.1016/j.bone.2020.115602. Epub 2020 Aug 22.

Abstract

BMPs were purified from demineralized bone matrix based on their ability to induce new bone in vivo and they represent a large member of the TGF-β superfamily of proteins. BMPs serve as morphogenic signals for mesenchymal stem cell migration, proliferation and subsequently differentiation into cartilage and bone during embryonic development. A BMP when implanted with a collagenous carrier in a rat subcutaneous site is capable of inducing new bone by mimicking the cellular events of embryonic bone formation. Based on this biological principle, BMP2 and BMP7 containing collagenous matrix as carrier have been developed as bone graft substitutes for spine fusion and long bone fractures. Here, we describe a novel autologous bone graft substitute that contains BMP6 delivered within an autologous blood coagulum as carrier and summarize the biology of osteogenic BMPs in the context of bone repair and regeneration specifically the critical role that carrier plays to support osteogenesis.

Keywords: BMP; BMP carrier; Bone formation; Bone repair.

Publication types

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

MeSH terms

  • Animals
  • Biology
  • Bone Morphogenetic Protein 2*
  • Bone Morphogenetic Protein 7
  • Bone Morphogenetic Proteins
  • Bone Regeneration
  • Bone Substitutes*
  • Cell Differentiation
  • Osteogenesis
  • Rats
  • Transforming Growth Factor beta

Substances

  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Protein 7
  • Bone Morphogenetic Proteins
  • Bone Substitutes
  • Transforming Growth Factor beta