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J Appl Physiol 103: 1873-1878, 2007. First published August 23, 2007; doi:10.1152/japplphysiol.00367.2007
8750-7587/07 $8.00
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INNOVATIVE METHODOLOGY

Vascular endothelial sampling and analysis of gene transcripts: a new quantitative approach to monitor vascular inflammation

Duygu Onat,1 Sanja Jelic,1 Ann Marie Schmidt,3 John Pile-Spellman,2 Shunichi Homma,1 Margherita Padeletti,1 Zhezhen Jin,4 Thierry H. Le Jemtel,5 Paolo C. Colombo,1,* and Lei Feng2,*

Departments of 1Medicine, 2Radiology, 3Surgery, and 4Biostatistics, Columbia University, New York, New York; and the 5Department of Medicine, Tulane University, New Orleans, Louisiana

Submitted 5 April 2007 ; accepted in final form 13 August 2007

Background: Limited access to endothelial tissue is a major constraint when investigating the cellular mechanisms of vascular inflammation in patients with cardiovascular and metabolic diseases. We introduce venous endothelial sampling coupled to quantitative analysis of gene transcripts by real-time PCR, as a novel approach to study endothelial gene expression in human subjects. Methods: Endothelial cells were collected from a superficial forearm vein using five guide wires sequentially inserted through a 20-gauge angiocatheter in seven patients with history of cardiovascular events related to advanced vascular disease and in 17 healthy subjects. Endothelial cells were purified using magnetic beads coated with endothelial specific antibodies. Endothelial mRNA was amplified using RiboAmp HS RNA Amplification kit (Molecular Devices, Sunnyvale, CA). Amplified RNA was analyzed by real-time PCR. Results: Linearity of RNA amplification was validated by real-time PCR using RNA from 1,000 human umbilical endothelial cells (HUVECs) before and after amplification. In human subjects, vascular disease was associated with significant induction of proatherosclerotic genes: early growth response gene product (Egr-1) and monocyte chemoattractant protein-1 (MCP-1). Conclusion: Venous endothelial sampling coupled to real-time PCR analysis is a minimally invasive, safe, and reliable technique to monitor vascular inflammation in human subjects. Expression of genes implicated in the atherosclerotic process is increased in the venous endothelium of patients with arterial vascular disease. Venous endothelial sampling and quantitative analysis of gene expression may help develop new vascular-targeted biomarkers to identify and track the impact of disease states and therapeutic interventions in vascular diseases.

inflammation; vein; vascular biology



Address for reprint requests and other correspondence: P. C. Colombo, Division of Cardiology, New York-Presbyterian Hospital/Columbia Univ. Medical Center, 622W 168th St., PH 12-134, New York, NY 10032 (e-mail: pcc2001{at}columbia.edu)







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