Capillary vessel network integration by inserting a vascular pedicle enhances bone formation in tissue-engineered bone using interconnected porous hydroxyapatite ceramics

Tissue Eng. 2004 May-Jun;10(5-6):789-95. doi: 10.1089/1076327041348338.

Abstract

The aim of the present study was to investigate the possibility of integrating porous hydroxyapatite (HA) ceramics with a capillary vessel network via insertion of a vascular pedicle, and to determine whether this procedure enhances new bone formation in tissue engineering of bone. First, synthetic interconnected porous HA (IP-CHA) was implanted subcutaneously into rat groin with or without insertion of superficial inferior epigastric vessels. At 6 weeks, IP-CHA with vascular insertion contained thick fibrous connective tissue with a number of large blood vessels that seemed to derive from the inserted vascular bundle. Next, IP-CHA loaded with recombinant human bone morphogenetic protein 2 (BMP, 2 or 10 microg/block) was implanted with or without vascular insertion. At 3 weeks, IP-CHA/BMP (10 microg) composite with vascular insertion exhibited abundant new bone formation in the pores of the deep portion close to the inserted vessels. In contrast, IP-CHA/BMP (10 microg) without vascular insertion showed poor bone formation. Histomorphometric analysis demonstrated that vascular insertion significantly increased new bone formation. In IP-CHAs with a lower dose of BMP (2 microg), no bone formation was found, with or without vascular insertion. These results suggest that the present system of integrating a vascular network with IP-CHA is a useful technique for bone tissue engineering.

Publication types

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

MeSH terms

  • Animals
  • Bone Substitutes*
  • Bone and Bones / blood supply*
  • Bone and Bones / cytology
  • Bone and Bones / drug effects
  • Bone and Bones / physiology*
  • Capillaries / transplantation*
  • Ceramics
  • Drug Delivery Systems / methods
  • Drug Implants
  • Durapatite
  • Growth Substances / pharmacology
  • Implants, Experimental
  • Male
  • Osteogenesis / drug effects
  • Osteogenesis / physiology*
  • Porosity
  • Rats
  • Rats, Sprague-Dawley
  • Tissue Engineering / methods*
  • Transplants

Substances

  • Bone Substitutes
  • Drug Implants
  • Growth Substances
  • Durapatite