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J Am Coll Cardiol, 2007; 50:2369-2374, doi:10.1016/j.jacc.2007.08.048 (Published online 11 December 2007).
© 2007 by the American College of Cardiology Foundation
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High Telomerase Activity in Neutrophils From Unstable Coronary Plaques

Maria Lucia Narducci, MD*,*, Annalisa Grasselli, PhD*, Luigi Marzio Biasucci, MD, FACC*, Antonella Farsetti, MD||, Antonino Mulè, MD{dagger}, Giovanna Liuzzo, MD*, Giuseppe La Torre, MD§, Giampaolo Niccoli, MD*, Rocco Mongiardo, MD*, Alfredo Pontecorvi, MD{ddagger} and Filippo Crea, MD, FACC*

* Institute of Cardiology
{dagger} Division of Anatomic Pathology and Histology
{ddagger} Institute of Medical Pathology
§ Institute of Hygiene, Catholic University of Sacred Heart, Rome, Italy
|| Neurobiology and Molecular Medicine Institute, National Council of Research, Rome, Italy
Department of Experimental Oncology, Regina Elena Cancer Institute, Rome, Italy


Figure 1
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Figure 1 Immunostaining of Coronary Plaque PMN With Myeloperoxidase Antibodies

Immunostaining for myeloperoxidase MPO-7 antibodies (purple) reveals staining of all cells isolated by direct washing of angioplasty balloon used for coronary revascularization, indicating that MPO-7–positive cells are neutrophils (arrow). Original magnification: x444. PMN = polymorphonuclear neutrophils.

 

Figure 2
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Figure 2 High Telomerase Activity in Coronary Plaque PMN of Patients With UA

Cell extracts derived from polymorphonuclear neutrophils (PMN) isolated from arterial (A) or venous blood (V) or directly from angioplasty balloons (AB) of unstable angina (UA) and chronic stable angina (SA) patients were assayed for telomerase activity by telomeric repeat amplification protocol assay in the presence of internal control (IC) (36 base pairs). As positive and negative controls, cell extracts (0.1 µg) from telomerase-positive HeLa cells were assayed before and after heat inactivation (HeLa and HeLa H.I.), respectively. Panels relative to the IC are shown at a lower detection exposure. Telomerase activity was barely detectable in PMN of patients with chronic SA (lanes 1 to 6, 13, and 14) and in arterial and venous PMN in patients with UA (lanes 8 and 9 and 11 and 12). In contrast, telomerase activity was high in PMN from the coronary atherosclerotic plaques in patients with UA (lanes 7 and 10).

 

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Figure 3 Distribution of Telomerase Activity

Telomerase activity in polymorphonuclear neutrophils derived from venous blood (V) or from washing medium of angioplasty balloons (AB) is represented as dot plots.

 

Figure 4
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Figure 4 Linear Regression Between Telomerase Activity And Timing of PCI

Among unstable angina patients, a significant inverse correlation was found between telomerase activity (ln: natural logarithm) in polimorphonuclear neutrophils obtained by atherosclerotic plaques and time interval (h) between last anginal episode and polimorphonuclear neutrophils sampling, during percutaneous coronary intervention (PCI).

 




 
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