Literature DB >> 23171225

Dual origin, development, and fate of bovine pancreatic islets.

Claudia Merkwitz1, Paul Lochhead, Jan Böttger, Madlen Matz-Soja, Michiharu Sakurai, Rolf Gebhardt, Albert M Ricken.   

Abstract

Endocrine cells are evident at an early stage in bovine pancreatic development when the pancreas still consists of primitive epithelial cords. At this stage, the endocrine cells are interspersed between the precursor cells destined to form the ductulo-acinar trees of later exocrine lobules. We here demonstrate that, in bovine fetuses of crown rump length ≥ 11 cm, the endocrine cells become increasingly segregated from the developing exocrine pancreas by assembly into two units that differ in histogenesis, architecture, and fate. Small numbers of 'perilobular giant islets' are distinguishable from larger numbers of 'intralobular small islets'. The two types of islets arise in parallel from the ends of the ductal tree. Aside from differences in number, location, and size, the giant and small islets differ in cellular composition (predominantly insulin-synthesising cells vs. mixtures of endocrine cells), morphology (epithelial trabeculae with gyriform and rosette-like appearance vs. compact circular arrangements of endocrine cells), and in their relationships to intrapancreatic ganglia and nerves. A further difference becomes apparent during the antenatal period; while the 'interlobular small islets' persist in the pancreata of calves and adult cattle, the perilobular giant islets are subject to regression, characterised by involution of the parenchyma, extensive haemorrhage, leukocyte infiltration (myeloid and T-cells) and progressive fibrotic replacement. In conclusion, epithelial precursor cells of the ductolo-acinar tree may give rise to populations of pancreatic islets with different histomorphology, cellular composition and fates. This should be taken into account when using these cells for the generation of pancreatic islets for transplantation therapy.
© 2012 The Authors Journal of Anatomy © 2012 Anatomical Society.

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Year:  2012        PMID: 23171225      PMCID: PMC3582255          DOI: 10.1111/joa.12014

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  63 in total

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6.  Neuroinsular complex type I: morphology and frequency in lean and genetically obese mice.

Authors:  S Persson-Sjögren
Journal:  Pancreas       Date:  2001-07       Impact factor: 3.327

7.  Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.

Authors:  S A Kassem; I Ariel; P S Thornton; I Scheimberg; B Glaser
Journal:  Diabetes       Date:  2000-08       Impact factor: 9.461

8.  Immunohistochemical localization of neuropeptides in bovine pancreas.

Authors:  T Myojin; N Kitamura; E Hondo; E T Baltazar; G T Pearson; J Yamada
Journal:  Anat Histol Embryol       Date:  2000-06       Impact factor: 1.114

9.  In vitro cultivation of human islets from expanded ductal tissue.

Authors:  S Bonner-Weir; M Taneja; G C Weir; K Tatarkiewicz; K H Song; A Sharma; J J O'Neil
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-05       Impact factor: 11.205

10.  Morphology and morphometry of in vivo- and in vitro-produced bovine concepti from early pregnancy to term and association with high birth weights.

Authors:  Marcelo Bertolini; Jeffrey B Mason; Stephen W Beam; Gustavo F Carneiro; Matthew L Sween; Daniel J Kominek; Alice L Moyer; Thomas R Famula; Roberto D Sainz; Gary B Anderson
Journal:  Theriogenology       Date:  2002-09       Impact factor: 2.740

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