The effect of covalent cross-links between the membrane components of microcapsules on the dissemination of encapsulated malignant cells

Biomaterials. 2008 Mar;29(7):917-24. doi: 10.1016/j.biomaterials.2007.10.045. Epub 2007 Nov 26.

Abstract

Stem cells and immortalized cells have considerable therapeutic potential but present risks of malignant transformation. Cell microencapsulation allows transplantation without immunosuppression. We have developed a method for microencapsulating living cells within covalently cross-linked membranes that are chemically and mechanically extremely resistant. We provide herein direct evidence that these microcapsules can prevent malignant cell dissemination. When 20,000 or more nonencapsulated EL-4 thymoma cells were implanted intraperitoneally in mice, all recipients died with widespread metastasis within 26.3+/-1.0 days. All recipients of 250,000 EL-4 cells microencapsulated in covalently cross-linked membranes were living and disease-free, 150 days post-implantation. Encapsulation in standard microcapsules only slightly delayed the recipient death. Pancreatic islets transplanted using either type of microcapsule presented similar survival. We conclude that microencapsulation in covalently cross-linked membranes prevents malignant cell dissemination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Capsules
  • Cell Line, Tumor
  • Cell Survival
  • Cross-Linking Reagents / chemistry*
  • Islets of Langerhans / cytology
  • Male
  • Mice
  • Models, Biological
  • Thy-1 Antigens / metabolism
  • Thymoma* / metabolism
  • Thymoma* / pathology
  • Thymus Neoplasms* / metabolism
  • Thymus Neoplasms* / pathology

Substances

  • Biomarkers
  • Capsules
  • Cross-Linking Reagents
  • Thy-1 Antigens