Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.4.24.17 (MMP-3)
 3,419 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Rous sarcoma virus-transformed rat liver cell line RSV-BRL secreted a neutral proteinase in a latent precursor form with a molecular weight (Mr) of 57,000 (57k) as a major secreted protein. This enzyme was a calcium-dependent metallo-proteinase. The proenzyme was purified from the serum-free conditioned medium of the transformed cells by affinity chromatographies on a zinc chelate Sepharose column and a reactive red agarose column. When activated by treatment with trypsin or p-aminophenylmercuric acetate (APMA) in the presence of Ca2+, the purified enzyme effectively hydrolyzed casein, fibronectin, and laminin. Type IV collagen was hydrolyzed at 37 degrees C but not at 30 degrees C by the enzyme, whereas type I and type III collagens were hardly hydrolyzed even at 37 degrees C. The treatment with trypsin or AMPA in the presence of Ca2+ converted this 57k proenzyme to an active and stable enzyme with Mr 42k. In the absence of Ca2+, however, APMA converted the proenzyme to an intermediate form with Mr 45k, while trypsin digested it to an inactive peptide with Mr 30k. These results demonstrate that calcium ion is essential for the activation, activity expression, and stabilization of this metallo-proteinase. Analysis of its partial amino acid sequence and amino acid composition showed that the 57k proenzyme was identical or closely related to the putative protein transin, a rat homologue of stromelysin.
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PMID:Purification and properties of extracellular matrix-degrading metallo-proteinase overproduced by Rous sarcoma virus-transformed rat liver cell line, and its identification as transin. 196 30

FR3T3 rat embryo fibroblast cells express preproenkephalin mRNA after transformation by polyoma virus middle T or Ha-ras oncogenes. This effect was not seen in another rat embryo fibroblast cell line (Rat-1) or in FR3T3 cells transformed by Rous sarcoma virus, bovine papilloma virus type I or SV40. The elevation in preproenkephalin mRNA levels is thus cell specific and oncogene specific. These results contrast with those obtained for transin mRNA, which was observed in both Rat-1 and FR3T3 cells transformed by a number of different oncogenes. The expression of transin RNA correlated with the expression of the transformed phenotype. We suggest that genes induced by oncogenes in a given cell will fall into two classes: those linked to the expression of the transformed phenotype (expression induced by all oncogenes conferring this phenotype) and those induced as a consequence of activation of a specific cellular signaling system (expression induced by a subset of oncogenes linked to the signaling system in question). This system may prove useful in distinguishing oncogene-induced events that are related to cellular transformation from those that are secondary to eliciting the transformed phenotype.
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PMID:Differential expression of preproenkephalin and transin mRNAs following oncogenic transformation: evidence for two classes of oncogene induced genes. 283 38

The aim of the present study is to clarify whether the cellular expression of a matrix-degrading metalloproteinase, transin, alters the behavior of cultured mesangial cells (MCs). The cDNA encoding rat transin was introduced into rat MCs and transcribed under the control of a Rous sarcoma virus promoter. The resulting transfectants were then investigated for cell shape, migration, proliferation, and expression of genes associated with matrix metabolism. Northern blot analysis routinely detected the transin transcript in two separate transfectants, MeTRN2 and MeTRN5. Transin expression was strong in MeTRN2, moderate in MeTRN5, but absent in mock transfectants. Immunoblot analysis revealed that these transin transfectants synthesized 59 and 62 kDa molecules, which correspond to transin gene products. Casein digestion assay detected enhanced proteolytic activity in MeTRN2 and MeTRN5. Microscopically, the transfected cells were somewhat elongated with accentuated margins compared with mock transfectants. [3H]-thymidine uptake studies revealed accelerated growth of the transfectants on a plastic substratum as well as within gel matrix. The migration of the transfectants into gel matrix was also significantly enhanced compared with that of mock transfectants. No obvious alteration, however, was found in transcripts of procollagen alpha 1(IV), laminin B2, or the metalloproteinase inhibitor TIMP. We hypothesize that the metalloproteinase transin has a potential for affecting the behavior of MCs and contributing to the pathogenesis of glomerular injury.
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PMID:Gene transfer of metalloproteinase transin induces aberrant behavior of cultured mesangial cells. 793 5