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J Thorac Cardiovasc Surg 2005;130:877
© 2005 The American Association for Thoracic Surgery


Brief Communication

Expression of the erythropoietin receptor in human heart

Reinhard Depping, PhD a , Katsuhiro Kawakami, MD c , Hartmut Ocker, MD c , Johannes M. Wagner, MD d , Matthias Heringlake, MD c , Axel Noetzold, MD b , Hans-Hinrich Sievers, MD b , Klaus F. Wagner, MD c , *

a Department of Physiology, University Luebeck, Luebeck, Germany
b Clinic of Cardiac Surgery, University Luebeck, Luebeck, Germany
c Clinic of Anesthesiology, University Luebeck, Luebeck, Germany
d Kidney Center Duisburg, Duisburg, Germany

Received for publication December 20, 2004; accepted for publication December 27, 2004.

* Address for reprints: Klaus F. Wagner, MD, Department of Anesthesiology, University Luebeck, Ratzeburger Allee 160, D-23538 Luebeck, Germany (Email: wagner@physio.uni-luebeck.de).

The first 20% of the full text of this article appears below.


Figure 1
Dr Wagner


Erythropoietin (EPO), the kidney hormone regulating erythrocyte production, activates the erythropoietin receptor (EPOR), resulting in antiapoptosis. To investigate the clinical significance of EPOR expressed in neuronal cells of the brain, EPO was administered to patients within 8 hours of the onset of stroke symptoms, which ultimately resulted in the reduction of cerebral infarct size and improvement of functional neurologic performance. 1 Go

Rodents treated with EPO in an animal model of myocardial ischemia and infarction recently demonstrated superior myocardial function. 2,3 Go The expression of the EPOR was shown for a variety of rodent and rabbit primary and permanent cardiomyocyte cell lines. But, as noted by several investigators, 2,3 Go proof of the presence of the EPOR in the adult human heart is missing.

To overcome this deficit, we investigated adult human ventricular and atrial tissue for the expression of the EPOR.

Methods

The study was approved by the institutional review board, and written informed consent was obtained from all participants. In patients with severe aortic valvular stenosis (valve area < 0.7 cm2), ventricular tissue was obtained from the muscular septum obstructing the left ventricular outflow tract (Morrow procedure) and snap-frozen for RNA and protein analysis or formalin-fixed for immunohistologic analysis (n = 4 per group). Right atrial tissue from the site of the venous cannulation was processed accordingly. Samples were analyzed with reverse transcriptase-polymerase chain reaction, Western blot, and standard or double immunohistochemistry as described in the online supplement.

Results and Discussion

In this report we provide evidence of the expression of the EPOR in adult human ventricular and atrial tissue. Western blots (Figure 1) and reverse transcriptase-polymerase chain reaction (Figure E1) from human ventricular and atrial tissue homogenates indicate the . . . [Full Text of this Article]




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