Methods of human islet culture for transplantation

Cell Transplant. 2004;13(6):605-17.

Abstract

The ability to maintain isolated human islet preparations in tissue culture has recently been adopted by most islet transplant centers, and improves the safety as well as the practicality of islet transplantation. Maintaining islet viability and recovery, however, remains challenging in a clinical setting, due to stringent conditions required for culture. Islet culture is further complicated by the fact that islets do not form a monolayer. This review aims to clarify media, supplementation, and conditions that have been shown to be relevant to human islets, as well as to offer avenues of future research. Factors examined that may influence islet survival include base medium, glucose concentration, vitamin, inorganic ion, lipid, hormone, growth factor, amino acid, and binding protein composition and concentration, as well as culture temperature and seeding density. In addition, this article reviews novel techniques, such as coculture and matrices, that have been employed in an attempt to improve islet survival and functional viability.

Publication types

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

MeSH terms

  • Amino Acids / metabolism
  • Amino Acids / pharmacology
  • Cations / metabolism
  • Cations / pharmacology
  • Cell Survival / drug effects
  • Culture Media / chemistry
  • Culture Media / pharmacology
  • Glucose / metabolism
  • Glucose / pharmacology
  • Growth Substances / metabolism
  • Growth Substances / pharmacology
  • Hormones / metabolism
  • Hormones / pharmacology
  • Humans
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / metabolism*
  • Islets of Langerhans Transplantation / methods*
  • Lipids / pharmacology
  • Tissue Culture Techniques / methods*
  • Vitamins / pharmacology

Substances

  • Amino Acids
  • Cations
  • Culture Media
  • Growth Substances
  • Hormones
  • Lipids
  • Vitamins
  • Glucose