Literature DB >> 396132

Sucrase and cellular development.

N Kretchmer, J S Latimer, F Raul, K Berry, C Legum, H L Sharp.   

Abstract

The cellular changes that take place as the intestinal cell migrates from crypt to villus are morphologically and biochemically remarkable. It is fortunate that many of these phenomena can be delineated by following enzymic activities. Sucrase-isomaltase is a particularly fascinating enzyme complex because it is a marker of the differentiated cell. Sucrase is inducible with steroids and protected by the substrate sucrose. Purified enzyme can be used to stimulate production of specific antibodies in goats; these antibodies have been used as probes to locate enzymically active and inactive antigen in the cells of the crypt and villus respectively. Further examination of the enzyme has indicated a molecular weight of 200 000--350 000. These higher molecular weight components are located in the brush border of the enterocytes. Lower molecular weight subunits are antigenically active and are in the cytosol. It is assumed that these smaller components are enzymically inactive pre-combination subunits of the sucrase-isomaltase complex and that the sucrase-isomaltase of the brush border is an aggregate of these subunits. The California sea lion, which is deficient in intestinal sucrase activity, does have isomaltase activity. This finding supports the concept that there are different gene complexes for sucrase and for isomaltase.

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Year:  1979        PMID: 396132     DOI: 10.1002/9780470720530.ch7

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  2 in total

1.  Jejunal mucosal DNA content and maturation. Inverse relation to serum gastrin levels in suckling and weanling rats.

Authors:  J E De Vries; W D Ford; R U Boelhouwer; W W King; J E Oscarson; J S Ross; J Thorell; R A Malt
Journal:  Dig Dis Sci       Date:  1985-11       Impact factor: 3.199

2.  Disaccharidase-deficient animals have normal ultrastructure of intestinal brush border membranes.

Authors:  J Bernstein; P Burrill; N Kretchmer
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

  2 in total

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