Literature DB >> 3279571

Large-scale production of fetal porcine pancreatic isletlike cell clusters. An experimental tool for studies of islet cell differentiation and xenotransplantation.

O Korsgren1, S Sandler, A S Landström, L Jansson, A Andersson.   

Abstract

A recently described method for the preparation of isletlike cell clusters (ICC) from human fetal pancreas has been applied to the fetal pig with the ultimate aim of large-scale production of ICC. Fetuses ranging in age from 51 to 77 days were used, and after a brief collagenase-incubation the pancreatic digest was plated into culture dishes containing medium RPMI 1640 supplemented with either 10% fetal calf serum (FCS) or human serum (HS). HS seemed to increase the number of ICC formed as compared to that obtained with FCS. A total of more than 100,000 ICC were produced from each of 3 litters, ages 67-77 days, after culture in the presence of HS. The DNA content of such ICC was reduced by about 50% as compared to those maintained with FCS supplementation. Immunocytochemical staining revealed insulin- and glucagon-positive cells scattered among a majority of nonstained cells within the cell clusters. ICC maintained in either FCS or HS displayed significant rates of (pro)insulin biosynthesis in vitro and an increased insulin release when exposed to 16.7 mM glucose plus 5 mM theophylline. Four weeks after implantation, ICC grafted under the kidney capsule of nondiabetic nude mice contained frequent insulin- and glucagon-positive cells. In 2 nude mice transplanted with ICC, the functional capacity of the graft was tested by perfusing the graft-bearing kidney. When the perfusion fluid was changed from one containing 2.8 mM glucose to one containing 16.7 mM glucose +/- 5 mM theophylline, the secretion of insulin increased within a few min. It is concluded that the fetal porcine pancreas can be used for large-scale production of ICC, which have a very consistent, but immature functional capacity. Because of their inherent growth and differentiation properties, fetal porcine ICC constitute a potential source of xenogenic islet grafts intended for human diabetics.

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Year:  1988        PMID: 3279571     DOI: 10.1097/00007890-198803000-00001

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  12 in total

1.  Enrichment of beta cells from the human fetal pancreas by fluorescence activated cell sorting with a new monoclonal antibody.

Authors:  R R de Krijger; H J Aanstoot; G Kranenburg; A Verkerk; J F Jongkind; R van Strik; K J Lafferty; G J Bruining
Journal:  Diabetologia       Date:  1992-05       Impact factor: 10.122

2.  Large scale isolation, growth, and function of porcine neonatal islet cells.

Authors:  G S Korbutt; J F Elliott; Z Ao; D K Smith; G L Warnock; R V Rajotte
Journal:  J Clin Invest       Date:  1996-05-01       Impact factor: 14.808

3.  Reactivity of human preformed natural antibodies with various porcine pancreatic cells.

Authors:  W Zhang; P Xiong; S Liu
Journal:  J Tongji Med Univ       Date:  2001

4.  Hyperglycemia-induced B cell toxicity. The fate of pancreatic islets transplanted into diabetic mice is dependent on their genetic background.

Authors:  O Korsgren; L Jansson; S Sandler; A Andersson
Journal:  J Clin Invest       Date:  1990-12       Impact factor: 14.808

5.  Functional and morphological differentiation of fetal porcine islet-like cell clusters after transplantation into nude mice.

Authors:  O Korsgren; L Jansson; D Eizirik; A Andersson
Journal:  Diabetologia       Date:  1991-06       Impact factor: 10.122

6.  The pig as the donor of pancreatic islets for men.

Authors:  M Trucco; A Casu; R Bottino
Journal:  Vet Res Commun       Date:  2007-08       Impact factor: 2.459

7.  Mumps virus infects beta cells in human fetal islet cell cultures upregulating the expression of HLA class I molecules.

Authors:  P Parkkonen; H Hyöty; L Koskinen; P Leinikki
Journal:  Diabetologia       Date:  1992-01       Impact factor: 10.122

8.  Ultrastructural evidence for blood microvessels devoid of an endothelial cell lining in transplanted pancreatic islets.

Authors:  A Lukinius; L Jansson; O Korsgren
Journal:  Am J Pathol       Date:  1995-02       Impact factor: 4.307

9.  Characterization of mixed syngeneic-allogeneic and syngeneic-xenogeneic islet-graft rejections in mice. Evidence of functional impairment of the remaining syngeneic islets in xenograft rejections.

Authors:  O Korsgren; L Jansson
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

10.  Islet cell transplantation today.

Authors:  Reinhard G Bretzel; Henning Jahr; Michael Eckhard; Isabel Martin; Daniel Winter; Mathias D Brendel
Journal:  Langenbecks Arch Surg       Date:  2007-03-28       Impact factor: 2.895

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