Journal of Histochemistry and Cytochemistry Priciples for Free Access to Science
  Search:   
    >> Advanced Search

Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact
Originally published as JHC exPRESS on October 16, 2006.
doi:10.1369/jhc.6A7050.2006
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jhc.6A7050.2006v1
55/2/141    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Segret, A.
Right arrow Articles by Renaud, J.-F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Segret, A.
Right arrow Articles by Renaud, J.-F.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Journal of Histochemistry and Cytochemistry
Volume 55 (2): 141-150, 2007
Copyright ©The Histochemical Society, Inc.

Structural Localization and Expression of CXCL12 and CXCR4 in Rat Heart and Isolated Cardiac Myocytes

Audrey Segret, Catherine Rücker-Martin, Catherine Pavoine, Jeanne Flavigny, Edith Deroubaix, Marc-Antoine Châtel, Alain Lombet and Jean-François Renaud

CNRS-UMR 8162, Université Paris-Sud, and Hôpital Marie Lannelongue, Le Plessis-Robinson, France (AS,CR-M,JF,ED,AL,J-FR); INSERM U581, Université Paris XII, and Hôpital Henri Mondor, Créteil, France (CP); and Département d'ophtalmologie 5, Hôpital XV–XX, Paris, France (M-AC)

Correspondence to: Audrey Segret, CNRS-UMR 8162, Université Paris XI Sud, Hôpital Marie Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France. E-mail: audrey.segret{at}ccml.u-psud.fr

CXCL12 (SDF-1), which binds CXCR4, is involved in several physiological and pathophysiological processes. In heart, this axis seems to play a key role in cardiogenesis and is involved in the neovascularization of ischemic tissues. Rats have three known CXCL12 mRNA isoforms, of which only {alpha} and {gamma} are present in the normal heart. However, little is known about CXCL12 protein expression and localization. We investigated the pattern of protein expression and the localization of both CXCR4 and CXCL12 in the heart, using isolated cardiomyocytes and a rat myocardial infarction model. Western blots showed that cardiomyocytes contained a specific 67-kDa CXCR4 isoform and a 12-kDa CXCL12 isoform. Confocal and electron microscopy clearly showed that CXCR4 was present at the plasmalemma and CXCL12 in continuity of the Z-line, in the proximal part of T-tubules. In conclusion, we provide the first description of the expression and fine localization of CXCR4 and CXCL12 proteins in normal rat heart and cardiomyocytes. These results suggest that the CXCL12/CXCR4 axis may be involved in cardiomyocyte calcium homeostasis regulation. Our work and the well-known chemoattraction properties of the CXCL12/CXCR4 axis highlight the importance of deciphering the function of this axis in both normal and pathological hearts. (J Histochem Cytochem 55:141–150, 2007)

Key Words: chemokine • CXCL12 • CXCR4 • heart • myocyte • T-tubules


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Physiol.Home page
J.-S. Lin, Y.-S. Chen, H.-S. Chiang, and M.-C. Ma
Hypoxic preconditioning protects rat hearts against ischaemia-reperfusion injury: role of erythropoietin on progenitor cell mobilization
J. Physiol., December 1, 2008; 586(23): 5757 - 5769.
[Abstract] [Full Text] [PDF]


Home page
ICVTSHome page
J. Tang, J. Wang, J. Yang, and X. Kong
Adenovirus-mediated stromal cell-derived- factor-1{alpha} gene transfer induces cardiac preservation after infarction via angiogenesis of CD133+ stem cells and anti-apoptosis
Interactive CardioVascular and Thoracic Surgery, October 1, 2008; 7(5): 767 - 770.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
Z. Pasha, Y. Wang, R. Sheikh, D. Zhang, T. Zhao, and M. Ashraf
Preconditioning enhances cell survival and differentiation of stem cells during transplantation in infarcted myocardium
Cardiovasc Res, January 1, 2008; 77(1): 134 - 142.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
V. F.M. Segers, T. Tokunou, L. J. Higgins, C. MacGillivray, J. Gannon, and R. T. Lee
Local Delivery of Protease-Resistant Stromal Cell Derived Factor-1 for Stem Cell Recruitment After Myocardial Infarction
Circulation, October 9, 2007; 116(15): 1683 - 1692.
[Abstract] [Full Text] [PDF]




Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact
The Journal of Histochemistry & Cytochemistry is owned, published, and licensed by The Histochemical Society © 2007