Literature DB >> 7695599

The role of meprin A in the pathogenesis of acute renal failure.

H Trachtman1, E Valderrama, J M Dietrich, J S Bond.   

Abstract

Meprin A is a zinc-dependent metallo-endopeptidase that is present in the brush border membrane of renal proximal tubular epithelial cells. Although this enzyme has been detected in the kidney of mammalian species and its biochemical structure and action have been characterized, the role of this endopeptidase in normal renal physiology and in disease states is unknown. Therefore, we assessed the susceptibility of inbred strains of mice with normal and low meprin A activity to ischemic and nephrotoxic acute renal failure. We report that two normal meprin A strains of mice, C57BL/6 and DBA/2, developed more severe renal functional and structural injury following either bilateral renal artery clamping or the injection of hypertonic glycerol, compared to two low meprin A strains, C3H/He and CBA. These findings suggest that meprin A plays a role in the pathophysiology of acute renal failure following a variety of insults to the kidney. We propose that redistribution of this metalloendopeptidase to the basolateral membrane domain during acute renal failure results in degradation of the extracellular matrix and damage to adjacent peritubular structures.

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Year:  1995        PMID: 7695599     DOI: 10.1006/bbrc.1995.1366

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  23 in total

1.  Meprin beta metalloprotease gene polymorphisms associated with diabetic nephropathy in the Pima Indians.

Authors:  Alexander R Red Eagle; Robert L Hanson; Weiping Jiang; Xiaoli Han; Gail L Matters; Giuseppina Imperatore; William C Knowler; Judith S Bond
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

Review 2.  Proteases: History, discovery, and roles in health and disease.

Authors:  Judith S Bond
Journal:  J Biol Chem       Date:  2019-02-01       Impact factor: 5.157

Review 3.  Meprin A metalloproteinase and its role in acute kidney injury.

Authors:  Gur P Kaushal; Randy S Haun; Christian Herzog; Sudhir V Shah
Journal:  Am J Physiol Renal Physiol       Date:  2013-02-20

4.  To be there when the picture is being painted.

Authors:  Judith S Bond
Journal:  J Biol Chem       Date:  2020-11-20       Impact factor: 5.157

5.  Identification of the cysteine residues implicated in the formation of alpha 2 and alpha/beta dimers of rat meprin.

Authors:  S Chevallier; J Ahn; G Boileau; P Crine
Journal:  Biochem J       Date:  1996-08-01       Impact factor: 3.857

6.  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

7.  Human meprin alpha and beta homo-oligomers: cleavage of basement membrane proteins and sensitivity to metalloprotease inhibitors.

Authors:  Markus-N Kruse; Christoph Becker; Daniel Lottaz; Danny Köhler; Irene Yiallouros; Hans-Willi Krell; Erwin E Sterchi; Walter Stöcker
Journal:  Biochem J       Date:  2004-03-01       Impact factor: 3.857

Review 8.  Meprins, membrane-bound and secreted astacin metalloproteinases.

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

9.  Critical amino acids in the active site of meprin metalloproteinases for substrate and peptide bond specificity.

Authors:  James P Villa; Greg P Bertenshaw; Judith S Bond
Journal:  J Biol Chem       Date:  2003-07-29       Impact factor: 5.157

10.  Targeted disruption of the meprin beta gene in mice leads to underrepresentation of knockout mice and changes in renal gene expression profiles.

Authors:  Lourdes P Norman; Weiping Jiang; Xiaoli Han; Thomas L Saunders; Judith S Bond
Journal:  Mol Cell Biol       Date:  2003-02       Impact factor: 4.272

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