Literature DB >> 2199965

Growing pancreatic acinar cells (postpancreatitis and fetal) express a ductal antigen.

R C De Lisle1, J H Grendell, J A Williams.   

Abstract

Monoclonal antibodies specific for luminal plasma membranes of acinar and duct cells of the exocrine pancreas were used to investigate changes in antigen expression during regeneration of the pancreas after acute pancreatitis and during fetal pancreatic development in mice. During regeneration after acute pancreatitis induced by supramaximal injections of cerulein or by a choline-deficient, ethionine-supplemented diet, morphologically identifiable acinar cells expressed the ductal antigen on their luminal surface, but at a lower level than this antigen is expressed on duct cells. As the pancreas regenerated, the ductal antigen was lost from acinar cells and was found only on duct cells. Characteristic tubular complexes formed in both pancreatitis models and were positive for the acinar antigen, demonstrating their acinar origin. In fetal pancreas, acinar cells between prenatal days 3 through 1, when zymogen granules were already abundant, expressed the duct-cell antigen on their luminal surface. By birth duct antigen was mostly present on ducts with only occasional label on acinar cells. The presence of a ductal antigen on acinar cells is associated with acinar-cell growth during regeneration and during fetal development and may reflect a less differentiated state.

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Year:  1990        PMID: 2199965     DOI: 10.1097/00006676-199007000-00002

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  6 in total

Review 1.  Redifferentiation and apoptosis of pancreatic cells during acute pancreatitis.

Authors:  J L Iovanna
Journal:  Int J Pancreatol       Date:  1996-10

2.  Establishment and immunocharacterization of an immortalized pancreatic cell line derived from the H-2Kb-tsA58 transgenic mouse.

Authors:  R Blouin; G Grondin; J Beaudoin; Y Arita; N Daigle; B G Talbot; D Lebel; J Morisset
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-10       Impact factor: 2.416

3.  Regeneration of the exocrine pancreas is delayed in telomere-dysfunctional mice.

Authors:  Guido von Figura; Martin Wagner; Kodandaramireddy Nalapareddy; Daniel Hartmann; Alexander Kleger; Luis Miguel Guachalla; Harshvardhan Rolyan; Guido Adler; Karl Lenhard Rudolph
Journal:  PLoS One       Date:  2011-02-22       Impact factor: 3.240

4.  Beta cell transdifferentiation does not contribute to preneoplastic/metaplastic ductal lesions of the pancreas by genetic lineage tracing in vivo.

Authors:  Oliver Strobel; Yuval Dor; Amy Stirman; Amanda Trainor; Carlos Fernández-del Castillo; Andrew L Warshaw; Sarah P Thayer
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-07       Impact factor: 11.205

5.  In vivo lineage tracing defines the role of acinar-to-ductal transdifferentiation in inflammatory ductal metaplasia.

Authors:  Oliver Strobel; Yuval Dor; Janivette Alsina; Amy Stirman; Gregory Lauwers; Amanda Trainor; Carlos Fernández-Del Castillo; Andrew L Warshaw; Sarah P Thayer
Journal:  Gastroenterology       Date:  2007-09-14       Impact factor: 22.682

6.  Caerulein-induced acute pancreatitis in mice that constitutively overexpress Reg/PAP genes.

Authors:  Oxana Norkina; Rolf Graf; Philippe Appenzeller; Robert C De Lisle
Journal:  BMC Gastroenterol       Date:  2006-05-15       Impact factor: 3.067

  6 in total

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