Literature DB >> 8660687

Expression and distribution of meprin protease subunits in mouse intestine.

J M Bankus1, J S Bond.   

Abstract

Meprins, zinc metalloendopeptidases of kidney and intestinal brush border membranes, are composed of differing ratios of alpha and beta subunits. Previous work indicated that the beta subunit was expressed in kidney and intestine of all mouse strains, but that the alpha subunit was only expressed in kidney of random-bred and some inbred strains and not in mouse intestine. The work herein, however, reports that low levels of meprin alpha subunit mRNA and protein are detectable in mouse intestine and are present in increasing concentrations from the duodenum to the ileum. In ICR mice, the duodenum expressed less than 1% of the meprin alpha mRNA (micrograms/g tissue) relative to kidney, the ileum approximately 20%. The large intestine contained approximately 10% of the message found in kidney. An inbred mouse strain, C3H/He, found previously to contain only meprin beta subunits in kidney and intestine, displayed very low levels of meprin alpha mRNA (approximately 1% of that in ICR kidney) in both the kidney and intestine. Intestinal meprin beta mRNA in ICR and C3H/He mice, by contrast, was expressed at similar levels to that found in kidney, and for both strains there was an increase (two- to threefold) in the beta message in the ileum relative to duodenum or jejunum. In general, the pattern of the meprin alpha protein along the intestine was similar to that of alpha mRNA, and activity and response of intestinal meprin A to inhibitors were typical of the enzyme isolated from kidney. These data indicate that meprin alpha can be detected in mouse small and large intestine and that expression is not only tissue- and strain-specific but also longitudinally variable in intestine. The expression pattern for both a and beta subunits indicates an ileal function for the meprins.

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Year:  1996        PMID: 8660687     DOI: 10.1006/abbi.1996.0286

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  8 in total

1.  MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease.

Authors:  S Banerjee; B Oneda; L M Yap; D P Jewell; G L Matters; L R Fitzpatrick; F Seibold; E E Sterchi; T Ahmad; D Lottaz; J S Bond
Journal:  Mucosal Immunol       Date:  2009-03-04       Impact factor: 7.313

Review 2.  Role of meprin metalloproteinases in cytokine processing and inflammation.

Authors:  Christian Herzog; Randy S Haun; Gur P Kaushal
Journal:  Cytokine       Date:  2018-12-20       Impact factor: 3.861

3.  Microbial-induced meprin β cleavage in MUC2 mucin and a functional CFTR channel are required to release anchored small intestinal mucus.

Authors:  André Schütte; Anna Ermund; Christoph Becker-Pauly; Malin E V Johansson; Ana M Rodriguez-Pineiro; Fredrik Bäckhed; Stefan Müller; Daniel Lottaz; Judith S Bond; Gunnar C Hansson
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-11       Impact factor: 11.205

4.  Villin and actin in the mouse kidney brush-border membrane bind to and are degraded by meprins, an interaction that contributes to injury in ischemia-reperfusion.

Authors:  Elimelda Moige Ongeri; Odinaka Anyanwu; W Brian Reeves; Judith S Bond
Journal:  Am J Physiol Renal Physiol       Date:  2011-07-27

5.  Identification of Mep1a as a susceptibility gene for atherosclerosis in mice.

Authors:  Andrew T Grainger; Nathanael Pilar; Jun Li; Mei-Hua Chen; Ashley M Abramson; Christoph Becker-Pauly; Weibin Shi
Journal:  Genetics       Date:  2021-12-10       Impact factor: 4.402

Review 6.  Meprins, membrane-bound and secreted astacin metalloproteinases.

Authors:  Erwin E Sterchi; Walter Stöcker; Judith S Bond
Journal:  Mol Aspects Med       Date:  2008-08-22

7.  Prointerleukin-18 is activated by meprin beta in vitro and in vivo in intestinal inflammation.

Authors:  Sanjita Banerjee; Judith S Bond
Journal:  J Biol Chem       Date:  2008-09-11       Impact factor: 5.157

8.  Proteolytic processing and inactivation of CCL2/MCP-1 by meprins.

Authors:  Christian Herzog; Randy S Haun; Sudhir V Shah; Gur P Kaushal
Journal:  Biochem Biophys Rep       Date:  2016-08-21
  8 in total

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