Insulin in tissue engineering of cartilage: a potential model system for growth factor application

J Drug Target. 2001;9(6):439-48. doi: 10.3109/10611860108998778.

Abstract

Investigation of novel experimental application systems for growth factors or other bioactive substances in tissue engineering is often limited by high costs of substances and would benefit from a defined and easily controllable model tissue system. Herein, we demonstrate a potential three-dimensional in vitro system using engineered cartilage as a model tissue and readily available insulin as a model drug. Previously it has been shown that insulin-like growth factor-I (IGF-I) has profound effects on tissue-engineered cartilage in vitro. Insulin is known to bind to the IGF-I receptor and to elicit significant responses in cartilage. In this study, bovine articular chondrocytes were seeded onto biodegradable polyglycolic acid (PGA) scaffolds and cultured for up to 7 weeks. Exogenous insulin (0.05-50 microg/ml) increased the growth rate and the glycosaminoglycan fraction of tissue-engineered cartilage, decreased the cell number in the tissue constructs, and improved the morphological appearance, with 2.5 microg/ml being the most favorable concentration. The observed effects of insulin were similar to effects of IGF-I (0.05 microg/ml) and were in agreement with the reported binding constants of IGF-I and insulin at the IGF-I receptor. Besides the possibility to employ insulin as a potent substance to improve tissue-engineered cartilage, the presented easily controllable in vitro system may be used in the future to evaluate experimental growth factor application devices using economically favorable insulin as a model protein.

MeSH terms

  • Animals
  • Biocompatible Materials
  • Cartilage / drug effects*
  • Cartilage / growth & development
  • Cattle
  • Cell Culture Techniques / methods
  • Chondrocytes / cytology
  • Chondrocytes / drug effects
  • Growth Substances / administration & dosage*
  • Growth Substances / pharmacology*
  • Insulin / administration & dosage*
  • Insulin / pharmacology*
  • Insulin-Like Growth Factor I / administration & dosage
  • Insulin-Like Growth Factor I / pharmacology
  • Models, Biological
  • Polymers / chemistry
  • Tissue Engineering / methods*

Substances

  • Biocompatible Materials
  • Growth Substances
  • Insulin
  • Polymers
  • Insulin-Like Growth Factor I