Autor: |
Tian, Bin, Carlyle, Wenda C., Weigold, W.Guy, McDonald, Kenneth M., Judd, Dianne L., Toher, Cynthia A., Homans, David C., Cohn, Jay N. |
Zdroj: |
Journal of Molecular and Cellular Cardiology; April 1999, Vol. 31 Issue: 4 p751-760, 10p |
Abstrakt: |
β-actin is a cytoskeletal protein that has been implicated as a potentially important mediator of the growth, signaling, migration, and remodeling of cells. Beta-actin is upregulated in remodeling myocardium in response to either pressure or volume overload. The cellular localization of this response has, however, not been determined and is a necessary first step to begin to clarify the role ofβ-actin in myocardial remodeling. Here we demonstrate thatβ-actin protein was confined primarily to the cardiac interstitium using immunofluorescent and immunohistochemical staining. Furthermore, both staining and immunoblotting showed markedly increasedβ-actin protein in myocardium within 24 h of either regional left ventricular damage or chronic volume overload. More importantly, this increase persisted up to 90 days in both models. Double staining showed co-localization ofβ-actin protein and von Willebrand factor, a specific endothelial cell marker. These results suggest that increasedβ-actin expression predominantly localized in cardiac interstitial cells, including endothelial cells. The increasedβ-actin could be due to either proliferation of the interstitial cells or upregulation of theβ-actin gene. |
Databáze: |
Supplemental Index |
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