Literature DB >> 7579699

The metalloproteinase matrilysin is preferentially expressed by epithelial cells in a tissue-restricted pattern in the mouse.

C L Wilson1, K J Heppner, L A Rudolph, L M Matrisian.   

Abstract

To explore the role of the matrix metalloproteinase matrilysin (MAT) in normal tissue remodeling, we cloned the murine homologue of MAT from postpartum uterus using RACE polymerase chain reaction and examined its pattern of expression in embryonic, neonatal, and adult mice. The murine coding sequence and the corresponding predicted protein sequence were found to be 75% and 70% identical to the human sequences, respectively, and organization of the six exons comprising the gene is similar to the human gene. Northern analysis and in situ hybridization revealed that MAT is expressed in the normal cycling, pregnant, and postpartum uterus, with levels of expression highest in the involuting uterus at early time points (6 h to 1.5 days postpartum). The mRNA was confined to epithelial cells lining the lumen and some glandular structures. High constitutive levels of MAT transcripts were also detected in the small intestine, where expression was localized to the epithelial Paneth cells at the base of the crypts. Similarly, MAT expression was found in epithelial cells of the efferent ducts, in the initial segment and cauda of the epididymis, and in an extra-hepatic branch of the bile duct. MAT transcripts were detectable only by reverse transcription-polymerase chain reaction in the colon, kidney, lung, skeletal muscle, skin, stomach, juvenile uterus, and normal, lactating, and involuting mammary gland, as was expression primarily late in embryogenesis. Analysis of MAT expression during postnatal development indicated that although MAT is expressed in the juvenile small intestine and reproductive organs, the accumulation of significant levels of MAT mRNA appears to correlate with organ maturation. These results show that MAT expression is restricted to specific organs in the mouse, where the mRNA is produced exclusively by epithelial cells, and suggest that in addition to matrix degradation and remodeling, MAT may play an important role in the differentiated function of these organs.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7579699      PMCID: PMC301245          DOI: 10.1091/mbc.6.7.851

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  61 in total

1.  Detection of CD1 mRNA in Paneth cells of the mouse intestine by in situ hybridization.

Authors:  J Lacasse; L H Martin
Journal:  J Histochem Cytochem       Date:  1992-10       Impact factor: 2.479

Review 2.  The matrix-degrading metalloproteinases.

Authors:  L M Matrisian
Journal:  Bioessays       Date:  1992-07       Impact factor: 4.345

3.  The role of the C-terminal domain in collagenase and stromelysin specificity.

Authors:  G Murphy; J A Allan; F Willenbrock; M I Cockett; J P O'Connell; A J Docherty
Journal:  J Biol Chem       Date:  1992-05-15       Impact factor: 5.157

4.  Expression and localization of the matrix metalloproteinase pump-1 (MMP-7) in human gastric and colon carcinomas.

Authors:  S McDonnell; M Navre; R J Coffey; L M Matrisian
Journal:  Mol Carcinog       Date:  1991       Impact factor: 4.784

5.  Molecular cloning of murine 72-kDa type IV collagenase and its expression during mouse development.

Authors:  P Reponen; C Sahlberg; P Huhtala; T Hurskainen; I Thesleff; K Tryggvason
Journal:  J Biol Chem       Date:  1992-04-15       Impact factor: 5.157

6.  Expression of the metalloproteinase matrilysin in DU-145 cells increases their invasive potential in severe combined immunodeficient mice.

Authors:  W C Powell; J D Knox; M Navre; T M Grogan; J Kittelson; R B Nagle; G T Bowden
Journal:  Cancer Res       Date:  1993-01-15       Impact factor: 12.701

7.  Molecular characterization of a low-molecular-mass matrix metalloproteinase secreted by glomerular mesangial cells as PUMP-1.

Authors:  H P Marti; L McNeil; G Thomas; M Davies; D H Lovett
Journal:  Biochem J       Date:  1992-08-01       Impact factor: 3.857

8.  Expression and localization of matrilysin, a matrix metalloproteinase, in human endometrium during the reproductive cycle.

Authors:  W H Rodgers; K G Osteen; L M Matrisian; M Navre; L C Giudice; F Gorstein
Journal:  Am J Obstet Gynecol       Date:  1993-01       Impact factor: 8.661

9.  Cryptdins: antimicrobial defensins of the murine small intestine.

Authors:  P B Eisenhauer; S S Harwig; R I Lehrer
Journal:  Infect Immun       Date:  1992-09       Impact factor: 3.441

10.  Enteric defensins: antibiotic peptide components of intestinal host defense.

Authors:  M E Selsted; S I Miller; A H Henschen; A J Ouellette
Journal:  J Cell Biol       Date:  1992-08       Impact factor: 10.539

View more
  42 in total

Review 1.  Antimicrobial peptides in innate intestinal host defence.

Authors:  R N Cunliffe; Y R Mahida
Journal:  Gut       Date:  2000-07       Impact factor: 23.059

Review 2.  The blood-epididymis barrier and inflammation.

Authors:  Mary Gregory; Daniel G Cyr
Journal:  Spermatogenesis       Date:  2014-12-31

3.  Alveolar heparan sulfate shedding impedes recovery from bleomycin-induced lung injury.

Authors:  W B LaRivière; S Liao; S A McMurtry; K Oshima; X Han; F Zhang; S Yan; S M Haeger; M Ransom; J A Bastarache; R J Linhardt; E P Schmidt; Y Yang
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2020-04-22       Impact factor: 5.464

4.  Increased susceptibility of aging kidney to ischemic injury: identification of candidate genes changed during aging, but corrected by caloric restriction.

Authors:  G Chen; E A Bridenbaugh; A D Akintola; J M Catania; V S Vaidya; J V Bonventre; A C Dearman; H W Sampson; D C Zawieja; R C Burghardt; A R Parrish
Journal:  Am J Physiol Renal Physiol       Date:  2007-08-01

Review 5.  Matrix metalloproteinases in lung: multiple, multifarious, and multifaceted.

Authors:  Kendra J Greenlee; Zena Werb; Farrah Kheradmand
Journal:  Physiol Rev       Date:  2007-01       Impact factor: 37.312

Review 6.  MMPs as therapeutic targets--still a viable option?

Authors:  Barbara Fingleton
Journal:  Semin Cell Dev Biol       Date:  2007-07-06       Impact factor: 7.727

7.  Intestinal tumorigenesis is suppressed in mice lacking the metalloproteinase matrilysin.

Authors:  C L Wilson; K J Heppner; P A Labosky; B L Hogan; L M Matrisian
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-18       Impact factor: 11.205

8.  Computational sequence analysis of matrix metalloproteinases.

Authors:  Q A Sang; D A Douglas
Journal:  J Protein Chem       Date:  1996-02

9.  The PEA3 subfamily of Ets transcription factors synergizes with beta-catenin-LEF-1 to activate matrilysin transcription in intestinal tumors.

Authors:  H C Crawford; B Fingleton; M D Gustavson; N Kurpios; R A Wagenaar; J A Hassell; L M Matrisian
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

10.  MMP7 shedding of syndecan-1 facilitates re-epithelialization by affecting alpha(2)beta(1) integrin activation.

Authors:  Peter Chen; Laura E Abacherli; Samuel T Nadler; Ying Wang; Qinglang Li; William C Parks
Journal:  PLoS One       Date:  2009-08-10       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.