Laminin-6 assembles into multimolecular fibrillar complexes with perlecan and participates in mechanical-signal transduction via a dystroglycan-dependent, integrin-independent mechanism
| Autor: | R C Geiger, Kevin P. Campbell, Kimberly Lane, Scott Budinger, Jonathan C.R. Jones, Meredith Gonzales, Susan B. Hopkinson, David A. Dean, Eduardo Correa-Meyer, Emilia Lecuona, Jacob I. Sznajder |
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| Rok vydání: | 2005 |
| Předmět: |
Male
MAPK/ERK pathway Integrins Integrin Perlecan Biology Lung injury Article Rats Sprague-Dawley Extracellular matrix Laminin Dystroglycan Animals Dystroglycans Protein Structure Quaternary Lung Cells Cultured Membrane Glycoproteins Epithelial Cells Cell Biology respiratory system Extracellular Matrix Rats Cell biology Protein Subunits Protein Transport Biochemistry Multiprotein Complexes biology.protein Signal transduction Heparan Sulfate Proteoglycans Protein Binding Signal Transduction |
| Zdroj: | Journal of Cell Science. 118:2557-2566 |
| ISSN: | 1477-9137 0021-9533 |
| DOI: | 10.1242/jcs.02395 |
| Popis: | Mechanical ventilation is a valuable treatment regimen for respiratory failure. However, mechanical ventilation (especially with high tidal volumes) is implicated in the initiation and/or exacerbation of lung injury. Hence, it is important to understand how the cells that line the inner surface of the lung [alveolar epithelial cells (AECs)] sense cyclic stretching. Here, we tested the hypothesis that matrix molecules, via their interaction with surface receptors, transduce mechanical signals in AECs. We first determined that rat AECs secrete an extracellular matrix (ECM) rich in anastamosing fibers composed of the alpha3 laminin subunit, complexed with beta1 and gamma1 laminin subunits (i.e. laminin-6), and perlecan by a combination of immunofluorescence microscopy and immunoblotting analyses. The fibrous network exhibits isotropic expansion when exposed to cyclic stretching (30 cycles per minute, 10% strain). Moreover, this same stretching regimen activates mitogen-activated-protein kinase (MAPK) in AECs. Stretch-induced MAPK activation is not inhibited in AECs treated with antagonists to alpha3 or beta1 integrin. However, MAPK activation is significantly reduced in cells treated with function-inhibiting antibodies against the alpha3 laminin subunit and dystroglycan, and when dystroglycan is knocked down in AECs using short hairpin RNA. In summary, our results support a novel mechanism by which laminin-6, via interaction with dystroglycan, transduces a mechanical signal initiated by stretching that subsequently activates the MAPK pathway in rat AECs. These results are the first to indicate a function for laminin-6. They also provide novel insight into the role of the pericellular environment in dictating the response of epithelial cells to mechanical stimulation and have broad implications for the pathophysiology of lung injury. |
| Databáze: | OpenAIRE |
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