Literature DB >> 9021726

Gelatinases and inhibitors of gelatinases in pancreatic islets and islet cell tumors.

T Tomita1, K Iwata.   

Abstract

Pancreatic islets contain trace amounts of zinc to form insulin dimer, and matrix metalloproteinases (MMPs) are single-chain zinc-containing metallo-enzymes. By immunocytochemically staining pancreatic tissue, which contained exocrine duct adenocarcinoma, normal islets were incidentally found positive for gelatinase-A (MMP-2) and gelatinase-B (MMP-9), and for tissue inhibitor of metalloproteinase 1 and 2 (TIMP-1 and TIMP-2). Normal islets from five pancreata were exclusively stained for two each of gelatinases and TIMPs. Twenty-two islet cell tumors were also stained for pancreatic hormones, gelatinases, and TIMPs, which included insulinomas, gastrinomas, glucagonomas, pancreatic polypeptide-omas (PPomas), and nonfunctioning tumor. In general, islet cell tumors were weakly stained for gelatinases and TIMPs, compared with normal islets in the adjacent pancreatic tissue. No clear difference in staining intensity among five kinds of islet cell tumors was observed. The selective immunolocalization of gelatinases and TIMPs in islet cells and islet cell tumors may suggest possible a structure-function relationship among zinc, gelatinases-TIMPs, and pancreatic hormones.

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Year:  1997        PMID: 9021726

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  11 in total

1.  Characterization of anti-TIMP-1 monoclonal antibodies for immunohistochemical localization in formalin-fixed, paraffin-embedded tissue.

Authors:  Irene Vejgaard Sorensen; Claus Fenger; Henrik Winther; Niels T Foged; Ulrik Lademann; Nils Brünner; Pernille A Usher
Journal:  J Histochem Cytochem       Date:  2006-03-03       Impact factor: 2.479

2.  Inhibition of Insulin-Degrading Enzyme Does Not Increase Islet Amyloid Deposition in Vitro.

Authors:  Meghan F Hogan; Daniel T Meier; Sakeneh Zraika; Andrew T Templin; Mahnaz Mellati; Rebecca L Hull; Malcolm A Leissring; Steven E Kahn
Journal:  Endocrinology       Date:  2016-07-12       Impact factor: 4.736

3.  Matrix Metalloproteinase-9 Protects Islets from Amyloid-induced Toxicity.

Authors:  Daniel T Meier; Ling-Hsien Tu; Sakeneh Zraika; Meghan F Hogan; Andrew T Templin; Rebecca L Hull; Daniel P Raleigh; Steven E Kahn
Journal:  J Biol Chem       Date:  2015-10-19       Impact factor: 5.157

4.  Immunocytochemical staining for islet amyloid polypeptide in pancreatic endocrine tumors.

Authors:  Tatsuo Tomita
Journal:  Islets       Date:  2011-11-01       Impact factor: 2.694

5.  Matrix metalloproteinases 2 and 9 are dispensable for pancreatic islet formation and function in vivo.

Authors:  Sabina E Perez; David A Cano; Trang Dao-Pick; Jean-Phillipe Rougier; Zena Werb; Matthias Hebrok
Journal:  Diabetes       Date:  2005-03       Impact factor: 9.461

6.  Matrix metalloproteinase-9 reduces islet amyloid formation by degrading islet amyloid polypeptide.

Authors:  Kathryn Aston-Mourney; Sakeneh Zraika; Jayalakshmi Udayasankar; Shoba L Subramanian; Pattie S Green; Steven E Kahn; Rebecca L Hull
Journal:  J Biol Chem       Date:  2012-12-10       Impact factor: 5.157

7.  Islet amyloid polypeptide in pancreatic islets from type 2 diabetic subjects.

Authors:  Tatsuo Tomita
Journal:  Islets       Date:  2012 May-Jun       Impact factor: 2.694

Review 8.  Apoptosis in pancreatic β-islet cells in Type 2 diabetes.

Authors:  Tatsuo Tomita
Journal:  Bosn J Basic Med Sci       Date:  2016-05-22       Impact factor: 3.363

9.  Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Pituitary Adenomas: Possible Markers of Neuroendocrine Cells.

Authors:  Tatsuo Tomita
Journal:  Endocr Pathol       Date:  1997       Impact factor: 3.943

10.  Immunocytochemical Localization of Glucose Transporter-2 (GLUT-2) in Pancreatic Islets and Islet Cell Tumors.

Authors:  Tatsuo Tomita
Journal:  Endocr Pathol       Date:  1999       Impact factor: 3.943

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