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Xenotransplantation of Embryonic Pig Kidney or Pancreas to Replace the Function of Mature Organs
Author(s) -
Marc R. Hammerman
Publication year - 2010
Publication title -
journal of transplantation
Language(s) - English
Resource type - Journals
eISSN - 2090-0015
pISSN - 2090-0007
DOI - 10.1155/2011/501749
Subject(s) - xenotransplantation , primordium , embryonic stem cell , islet , pancreas , transplantation , immunosuppression , medicine , pancreatic islets , organogenesis , kidney , miniature swine , immune system , biology , immunology , microbiology and biotechnology , andrology , insulin , biochemistry , gene
Lack of donor availability limits the number of human donor organs. The need for host immunosuppression complicates transplantation procedures. Ultrastructurally precise kidneys differentiate in situ following xenotransplantation in mesentery of embryonic pig renal primordia. The developing organ attracts its blood supply from the host, obviating humoral rejection. Engraftment of pig renal primordia transplanted directly into rats requires host immune suppression. However, insulin-producing cells originating from embryonic pig pancreas obtained very early following initiation of organogenesis [embryonic day 28 (E28)] engraft long term in nonimmune-suppressed diabetic rats or rhesus macaques. Engraftment of morphologically similar cells originating from adult porcine islets of Langerhans (islets) occurs in rats previously transplanted with E28 pig pancreatic primordia. Here, we review recent findings germane to xenotransplantation of pig renal or pancreatic primordia as a novel organ replacement strategy.

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