Mouse proximal tubular cell-cell adhesion inhibits apoptosis by a cadherin-dependent mechanism
Autor: | Jerrold S. Levine, Jason S. Koh, Eoin Bergin, Wilfred Lieberthal |
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Rok vydání: | 2000 |
Předmět: |
Programmed cell death
Physiology Morpholines Molecular Sequence Data Apoptosis Biology Kidney Tubules Proximal Mice Phosphatidylinositol 3-Kinases Cell–cell interaction Cell Adhesion Animals Anoikis Amino Acid Sequence Enzyme Inhibitors Cell adhesion Cells Cultured Phosphoinositide-3 Kinase Inhibitors Cadherin Kinase Adhesion Cadherins Peptide Fragments Cell biology Extracellular Matrix Enzyme Activation Microscopy Electron Biochemistry Chromones |
Zdroj: | American journal of physiology. Renal physiology. 278(5) |
ISSN: | 1931-857X |
Popis: | Adhesion of epithelial cells to matrix is known to inhibit apoptosis. However, the role of cell-cell adhesion in mediating cell survival remains uncertain. Primary cultures of mouse proximal tubular (MPT) cells were used to examine the role of cell-cell adhesion in promoting survival. When MPT cells were deprived of both cell-matrix and cell-cell adhesion, they died by apoptosis. However, when incubated in agarose-coated culture dishes (to prevent cell-matrix adhesion) and at high cell density (to allow cell-cell interactions), MPT cells adhered to one another and remained viable. Expression of E-cadherin among suspended, aggregating cells increased with time. A His-Ala-Val (HAV)-containing peptide that inhibits homophilic E-cadherin binding prevented cell-cell aggregation and promoted apoptosis of MPT cells in suspension. By contrast, inhibition of potential β1-integrin-mediated interactions between cells in suspension did not prevent either aggregation or survival of suspended cells. Aggregation of cells in suspension activated phosphatidylinositol 3-kinase (PI3K), an event that was markedly reduced by the presence of the HAV peptide. LY-294002, an inhibitor of PI3K, also inhibited survival of suspended cells. In summary, we provide novel evidence that MPT cells, when deprived of normal cell-matrix interactions, can adhere to one another in a cadherin-dependent fashion and remain viable. Survival of aggregated cells depends on activation of PI3K. |
Databáze: | OpenAIRE |
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