Literature DB >> 3989447

Clonal analysis of intestinal crypt populations in mouse aggregation chimaeras.

G H Schmidt, D J Garbutt, M M Wilkinson, B A Ponder.   

Abstract

The epithelium of each individual intestinal crypt in adult mouse aggregation chimaeras is composed of cells of a single parental genotype (Ponder et al. 1985). Using a carbohydrate polymorphism recognized by Dolichos biflorus agglutinin as a strain-specific marker on entire sheets of intestinal mucosa, we have analysed the two-dimensional mosaic patterns of patches of the chimaeric intestinal crypt population. The relative proportions of each genotype varied greatly along the length of any one intestine. In chimaeras with highly unbalanced proportions, the minority component occurred as discrete patches. Patches of single or a few crypts were most frequent, but a smaller number of much larger patches was always present. The size frequency distribution of discrete patches was highly concave and departed significantly from a geometric distribution (a model for non-differential proliferation), but fitted the more skewed negative binomial model. The data are consistent with the interpretation that most progenitor crypts never or rarely divide, while a minority proliferate to a greater extent. We discuss ways in which our system could be analysed further to examine this interpretation. Our results also support Whitten's (1978) conclusion from a computer simulation that the mean patch size, as it has previously been used in statistical analyses of chimaeric tissue, 'is not a reliable statistic on which to judge mosaicism'.

Entities:  

Mesh:

Year:  1985        PMID: 3989447

Source DB:  PubMed          Journal:  J Embryol Exp Morphol        ISSN: 0022-0752


  13 in total

Review 1.  Stem cell in gastrointestinal structure and neoplastic development.

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Review 2.  Adult intestinal stem cells: critical drivers of epithelial homeostasis and regeneration.

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3.  Quantitative analysis of cell allocation during liver development, using the spf(ash)-heterozygous female mouse.

Authors:  N Shiojiri; M Sano; S Inujima; M Nitou; M Kanazawa; M Mori
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4.  Mosaic analysis of small intestinal development using the spf(ash)-heterozygous female mouse.

Authors:  Nobuyoshi Shiojiri; Masataka Mori
Journal:  Histochem Cell Biol       Date:  2003-02-13       Impact factor: 4.304

Review 5.  Immunohistochemistry in the analysis of mouse aggregation chimaeras.

Authors:  B A Ponder; G H Schmidt; M M Wilkinson
Journal:  Histochem J       Date:  1986-05

6.  Chimeric analysis of EGFP and DsRed2 transgenic mice demonstrates polyclonal maintenance of pancreatic acini.

Authors:  Je-Young Ryu; Antoni Siswanto; Kenichi Harimoto; Yoh-ichi Tagawa
Journal:  Transgenic Res       Date:  2012-10-17       Impact factor: 2.788

7.  Chimeric mice reveal clonal development of pancreatic acini, but not islets.

Authors:  E Scott Swenson; Julie Xanthopoulos; Timothy Nottoli; James McGrath; Neil D Theise; Diane S Krause
Journal:  Biochem Biophys Res Commun       Date:  2008-12-29       Impact factor: 3.575

8.  Transgenic mice containing intestinal fatty acid-binding protein-human growth hormone fusion genes exhibit correct regional and cell-specific expression of the reporter gene in their small intestine.

Authors:  D A Sweetser; S M Hauft; P C Hoppe; E H Birkenmeier; J I Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

Review 9.  Multicolor lineage tracing methods and intestinal tumors.

Authors:  Hirotsugu Yanai; Toshihiro Tanaka; Hiroo Ueno
Journal:  J Gastroenterol       Date:  2013-01-11       Impact factor: 7.527

10.  Use of transgenic mice to map cis-acting elements in the intestinal fatty acid binding protein gene (Fabpi) that control its cell lineage-specific and regional patterns of expression along the duodenal-colonic and crypt-villus axes of the gut epithelium.

Authors:  S M Cohn; T C Simon; K A Roth; E H Birkenmeier; J I Gordon
Journal:  J Cell Biol       Date:  1992-10       Impact factor: 10.539

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