Literature DB >> 7149281

Light microscopic morphometric analysis of rat ileal mucosa: II. Component quantitation of Paneth cells.

C B Rodning, S L Erlandsen, I D Wilson, A M Carpenter.   

Abstract

A quantitative light microscopic morphometric analysis of lysozyme- and IgA-containing Paneth cells within the ileal mucosa of physiologically manipulated and control (sham operation) animals was performed. The experimental groups of rats included animals raised in a gnotobiotic environment (microbial reduction) and animals with ileal self-filling blind (microbial proliferation) and Thiry-Vella (intestinal discontinuity) loops. The unlabeled antibody enzyme immunohistochemical localization technique was employed for the identification of intracellular lysozyme and IgA. Component quantitation was performed by use of a micrometer component quantitator. Marked Paneth cell hyperplasia was noted in association with gnotobiosis and with the Thiry-Vella fistula. This observation quantitatively confirms previous subjective impressions of increased Paneth cell differentiation in association with those physiologic states. Since the neurovascular component of the Thiry-Vella fistula is intact, the normal intraluminal succus entericus would appear to be involved in modulation of Paneth cell differentiation. The recognition of Paneth cell hyperplasia in association with the Thiry-Vella fistula suggests that this may be a useful experimental model for an evaluation of the life cycle and functional characteristics of this cell population. The results also revealed that no significant change in the volume percentage of Paneth cells and a decreased volume percentage of Paneth cells containing IgA occurred in association with the self-filling blind loop. A decreased volume percentage of IgA-containing immunocytes in association with the blind loop has previously been reported. The data are most consistent with the interpretation that the Paneth cell and immunocyte response to antigenic stimulation are interrelated and that the Paneth cell population has a restricted latitude of response to microbial proliferation.

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Year:  1982        PMID: 7149281     DOI: 10.1002/ar.1092040105

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  8 in total

1.  Immunohistochemical observations of immunoglobulin A in the Paneth cells of germ-free and formerly-germ-free rats.

Authors:  Y Satoh; K Ishikawa; H Tanaka; K Ono
Journal:  Histochemistry       Date:  1986

2.  Effect of live and heat-killed bacteria on the secretory activity of Paneth cells in germ-free mice.

Authors:  Y Satoh
Journal:  Cell Tissue Res       Date:  1988-01       Impact factor: 5.249

3.  Bethanechol and a G-protein activator, NaF/AlCl3, induce secretory response in Paneth cells of mouse intestine.

Authors:  Y Satoh; K Ishikawa; Y Oomori; S Takeda; K Ono
Journal:  Cell Tissue Res       Date:  1992-08       Impact factor: 5.249

4.  Changes in the Paneth cell population of human small intestine assessed by image analysis of the secretory granule area.

Authors:  M E Elmes; J G Jones; M R Stanton
Journal:  J Clin Pathol       Date:  1983-08       Impact factor: 3.411

5.  Histopathological changes in the epithelial cells of rat duodenum following chronic dietary exposure to cadmium, with particular reference to Paneth cells.

Authors:  C J Phillpotts
Journal:  Br J Exp Pathol       Date:  1986-08

6.  Atropine inhibits the degranulation of Paneth cells in ex-germ-free mice.

Authors:  Y Satoh
Journal:  Cell Tissue Res       Date:  1988-08       Impact factor: 5.249

7.  The enteric microbiota regulates jejunal Paneth cell number and function without impacting intestinal stem cells.

Authors:  Alexi A Schoenborn; Richard J von Furstenberg; Smrithi Valsaraj; Farah S Hussain; Molly Stein; Michael T Shanahan; Susan J Henning; Ajay S Gulati
Journal:  Gut Microbes       Date:  2018-07-11

8.  Characterization of paneth cells in alpacas (Vicugna pacos, Mammalia, Camelidae).

Authors:  María Vásquez; Boris Lira; José Rodríguez; Néstor Falcón; Jorge Ocampo; Fabián Nishida; Claudio Barbeito; Carolina Zanuzzi
Journal:  Tissue Cell       Date:  2016-05-07       Impact factor: 2.466

  8 in total

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