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Issue 880 coverCELL AND MOLECULAR BIOLOGY OF PANCREATIC CARCINOMA: RECENT DEVELOPMENTS IN RESEARCH AND EXPERIMENTAL THERAPY Copyright © 1999 by the New York Academy of Sciences
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Articles by SCHNEKENBURGER, J.
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Articles by SCHNEKENBURGER, J.
Articles by LERCH, M. M.
Annals of the New York Academy of Sciences 880:157-165 (1999)
© 1999 New York Academy of Sciences

Protein Tyrosine Dephosphorylation and the Maintenance of Cell Adhesions in the Pancreas

J. SCHNEKENBURGER, J. MAYERLE, P. SIMON, W. DOMSCHKE AND M. M. LERCHa

Department of Medicine B, Westfälische Wilhelms-Universität, Münster, Germany

aAddress for correspondence: Dr. M. M. Lerch, Department of Medicine B. Westfälische Wilhelms Universität, Albert-Schweitzer-Strasse 33, 48129 Mü, Germany. Phone, +49 251-843-7559; fax, +49 251-49504; e-mail: markus.lerch{at}uni-muenster.de

Cell-cell contacts are important regulatory elements in tissue development, organ morphogenesis and malignant tumor invasion. In recent in vivo studies we have identified the members of the cadherin/catenin family of cell adhesion proteins that are differentially expressed in the pancreas and have determined their cell biological dynamics during dissociation and repair of adherens junctions. To further characterize these events, epithelial cell culture systems were used and a number of type II protein tyrosine phosphatases (PTPs) were found to colocalize and interact with the cadherin/catenin complex. These observations suggest that tyrosine dephosphorylation in general and PTPs in particular are involved in cell contact formation. Our most recent experiments indicate 1) that inhibition of PTPs alone dissociates pancreatic adherens junctions, 2) that cytosolic and transmembrane PTPs are differentially expressed in acinar cells, and 3) that a subset of them can associate with proteins of the cadherin/catenin complex at pancreatic cell-cell adhesions.




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