BACKGROUND: Xenotransplantation of porcine islets could be a valuable alternative to the shortage of human islets for transplantation. To overcome the immunological obstacle of antibody-mediated rejection, pigs homozygous for alpha1,3-galactosyltransferase gene knock-out (GT-KO) have been produced. The effect of this mutation on glucose metabolism is unknown. METHODS: Glucose, insulin, C-peptide and glucagon levels were studied in eight adult pigs (four wild-type [WT] and four GT-KO) during intravenous glucose tolerance test (IVGTT), arginine stimulation test (AST), and insulin tolerance test (ITT). Morphological analysis of the pancreata was also performed. The in vitro insulin response to a high glucose concentration and theophylline were studied in a dynamic perfusion system with isolated islets. RESULTS: Basal and stimulated blood glucose levels were similar in WT and GT-KO pigs. Basal insulin, C-peptide and glucagon were higher in GT-KO pigs. C-peptide and insulin responses to arginine and glucose were also higher in GT-KO animals. The reduction in blood glucose during ITT and IVGTT was similar in WT and GT-KO pigs. The extent of staining for insulin and glucagon in the pancreata were similar. The basal insulin secretion of isolated islets was higher in GT-KO pigs, while stimulation indexes for glucose and theophylline were similar to WT. CONCLUSIONS: GT-KO pigs demonstrated differences in glucose metabolism compared to WT pigs, the cause for which remains uncertain. It is unlikely that these differences would in any way affect the outcome of GT-KO porcine islet xenotransplantation.
BACKGROUND: Xenotransplantation of porcine islets could be a valuable alternative to the shortage of human islets for transplantation. To overcome the immunological obstacle of antibody-mediated rejection, pigs homozygous for alpha1,3-galactosyltransferase gene knock-out (GT-KO) have been produced. The effect of this mutation on glucose metabolism is unknown. METHODS:Glucose, insulin, C-peptide and glucagon levels were studied in eight adult pigs (four wild-type [WT] and four GT-KO) during intravenous glucose tolerance test (IVGTT), arginine stimulation test (AST), and insulin tolerance test (ITT). Morphological analysis of the pancreata was also performed. The in vitro insulin response to a high glucose concentration and theophylline were studied in a dynamic perfusion system with isolated islets. RESULTS: Basal and stimulated blood glucose levels were similar in WT and GT-KO pigs. Basal insulin, C-peptide and glucagon were higher in GT-KO pigs. C-peptide and insulin responses to arginine and glucose were also higher in GT-KO animals. The reduction in blood glucose during ITT and IVGTT was similar in WT and GT-KO pigs. The extent of staining for insulin and glucagon in the pancreata were similar. The basal insulin secretion of isolated islets was higher in GT-KO pigs, while stimulation indexes for glucose and theophylline were similar to WT. CONCLUSIONS: GT-KO pigs demonstrated differences in glucose metabolism compared to WT pigs, the cause for which remains uncertain. It is unlikely that these differences would in any way affect the outcome of GT-KO porcine islet xenotransplantation.
Authors: David K C Cooper; Shinichi Matsumoto; Adrian Abalovich; Takeshi Itoh; Nizar I Mourad; Pierre R Gianello; Eckhard Wolf; Emanuele Cozzi Journal: Transplantation Date: 2016-11 Impact factor: 4.939
Authors: Burcin Ekser; John Bianchi; Suyapa Ball; Hayato Iwase; Anneke Walters; Mohamed Ezzelarab; Massimiliano Veroux; Bruno Gridelli; Robert Wagner; David Ayares; David K C Cooper Journal: Xenotransplantation Date: 2012-11-12 Impact factor: 3.907
Authors: Martin Wijkstrom; Rita Bottino; Hayoto Iwase; Hidetaka Hara; Burcin Ekser; Dirk van der Windt; Cassandra Long; Frederico G S Toledo; Carol J Phelps; Massimo Trucco; David K C Cooper; David Ayares Journal: Xenotransplantation Date: 2014-11-10 Impact factor: 3.907
Authors: Danish Saleheen; Pradeep Natarajan; Irina M Armean; Wei Zhao; Asif Rasheed; Sumeet A Khetarpal; Hong-Hee Won; Konrad J Karczewski; Anne H O'Donnell-Luria; Kaitlin E Samocha; Benjamin Weisburd; Namrata Gupta; Mozzam Zaidi; Maria Samuel; Atif Imran; Shahid Abbas; Faisal Majeed; Madiha Ishaq; Saba Akhtar; Kevin Trindade; Megan Mucksavage; Nadeem Qamar; Khan Shah Zaman; Zia Yaqoob; Tahir Saghir; Syed Nadeem Hasan Rizvi; Anis Memon; Nadeem Hayyat Mallick; Mohammad Ishaq; Syed Zahed Rasheed; Fazal-Ur-Rehman Memon; Khalid Mahmood; Naveeduddin Ahmed; Ron Do; Ronald M Krauss; Daniel G MacArthur; Stacey Gabriel; Eric S Lander; Mark J Daly; Philippe Frossard; John Danesh; Daniel J Rader; Sekar Kathiresan Journal: Nature Date: 2017-04-12 Impact factor: 49.962
Authors: Dirk J van der Windt; Rita Bottino; Goutham Kumar; Martin Wijkstrom; Hidetaka Hara; Mohamed Ezzelarab; Burcin Ekser; Carol Phelps; Noriko Murase; Anna Casu; David Ayares; Fadi G Lakkis; Massimo Trucco; David K C Cooper Journal: Diabetes Date: 2012-12 Impact factor: 9.461
Authors: M Victoria Sanz Fernandez; Sara K Stoakes; Mohannad Abuajamieh; Jacob T Seibert; Jay S Johnson; Erin A Horst; Robert P Rhoads; Lance H Baumgard Journal: Physiol Rep Date: 2015-08