Caveolin modulates integrin function and mechanical activation in the cardiomyocyte. Issue 2 (3rd November 2014)
- Record Type:
- Journal Article
- Title:
- Caveolin modulates integrin function and mechanical activation in the cardiomyocyte. Issue 2 (3rd November 2014)
- Main Title:
- Caveolin modulates integrin function and mechanical activation in the cardiomyocyte
- Authors:
- Israeli‐Rosenberg, Sharon
Chen, Chao
Li, Ruixia
Deussen, Daniel N.
Niesman, Ingrid R.
Okada, Hideshi
Pately, Hemal H.
Roth, David M.
Ross, Robert S. - Abstract:
- ABSTRACT: β1 integrins (β1) transduce mechanical signals in many cells, including cardiac myocytes (CM). Given their close localization, as well as their role in mechanotransduction and signaling, we hypothesized that caveolin (Cav) proteins might regulate integrins in the CM. β1 localization, complex formation, activation state, and signaling were analyzed using wild‐type, Cav3 knockout, and Cav3 CM‐specific transgenic heart and myocyte samples. Studies were performed under basal and mechanically loaded conditions. We found that: 1) β1 and Cav3 colocalize in CM and coimmunoprecipitate from CM protein lysates; 2) β1 is detected in a subset of caveolae; 3) loss of Cav3 caused reduction of β1D integrin isoform and active β1 integrin from the buoyant domains in the heart; 4) increased expression of myocyte Cav3 correlates with increased active β1 integrin in adult CM; 5) in vivo pressure overload of the wild‐type heart results in increased activated integrin in buoyant membrane domains along with increased association between active integrin and Cav3; and 6) Cav3‐deficient myocytes have perturbed basal and stretch mediated signaling responses. Thus, Cav3 protein can modify integrin function and mechanotransduction in the CM and intact heart.—Israeli‐Rosenberg, S., Chen, C., Li, R., Deussen, D. N., Niesman, I. R., Okada, H., Patel, H. H., Roth, D. M., Ross, R. S. Caveolin modulates integrin function and mechanical activation in the cardiomyocyte. FASEB J . 29, 374‐384 (2015).ABSTRACT: β1 integrins (β1) transduce mechanical signals in many cells, including cardiac myocytes (CM). Given their close localization, as well as their role in mechanotransduction and signaling, we hypothesized that caveolin (Cav) proteins might regulate integrins in the CM. β1 localization, complex formation, activation state, and signaling were analyzed using wild‐type, Cav3 knockout, and Cav3 CM‐specific transgenic heart and myocyte samples. Studies were performed under basal and mechanically loaded conditions. We found that: 1) β1 and Cav3 colocalize in CM and coimmunoprecipitate from CM protein lysates; 2) β1 is detected in a subset of caveolae; 3) loss of Cav3 caused reduction of β1D integrin isoform and active β1 integrin from the buoyant domains in the heart; 4) increased expression of myocyte Cav3 correlates with increased active β1 integrin in adult CM; 5) in vivo pressure overload of the wild‐type heart results in increased activated integrin in buoyant membrane domains along with increased association between active integrin and Cav3; and 6) Cav3‐deficient myocytes have perturbed basal and stretch mediated signaling responses. Thus, Cav3 protein can modify integrin function and mechanotransduction in the CM and intact heart.—Israeli‐Rosenberg, S., Chen, C., Li, R., Deussen, D. N., Niesman, I. R., Okada, H., Patel, H. H., Roth, D. M., Ross, R. S. Caveolin modulates integrin function and mechanical activation in the cardiomyocyte. FASEB J . 29, 374‐384 (2015). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 29:Issue 2(2015)
- Journal:
- FASEB journal
- Issue:
- Volume 29:Issue 2(2015)
- Issue Display:
- Volume 29, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 2
- Issue Sort Value:
- 2015-0029-0002-0000
- Page Start:
- 374
- Page End:
- 384
- Publication Date:
- 2014-11-03
- Subjects:
- caveolae -- focal adhesions -- mechanotransduction -- myocardium
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.13-243139 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13226.xml