Thromb Haemost 2012; 107(04): 619-625
DOI: 10.1160/TH11-09-0607
Theme Issue Article
Schattauer GmbH

microRNA expression signatures and parallels between monocyte subsets and atherosclerotic plaque in humans

Kiril Bidzhekov
1   Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Munich, Munich, Germany
2   Institute of Molecular Cardiovascular Research (IMCAR), RWTH Aachen University, Aachen, Germany
,
Lin Gan
3   Interdisciplinary Centre for Clinical Research Aachen, RWTH Aachen University, Aachen, Germany
,
Bernd Denecke
3   Interdisciplinary Centre for Clinical Research Aachen, RWTH Aachen University, Aachen, Germany
,
André Rostalsky
1   Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Munich, Munich, Germany
,
Mihail Hristov
1   Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Munich, Munich, Germany
2   Institute of Molecular Cardiovascular Research (IMCAR), RWTH Aachen University, Aachen, Germany
,
Thomas A. Koeppel
4   Vascular Surgery, Ludwig-Maximilians-University Munich, Munich, Germany
,
Alma Zernecke
5   Rudolf-Virchow-Center/DFG-Research Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany
,
Christian Weber
1   Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Munich, Munich, Germany
6   Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands
7   Munich Heart Alliance, Munich, Germany
› Institutsangaben
Financial support: This work was supported by the Deutsche Forschungsgemeinschaft (ZE 827/4–1 to A.Z., ZE 827/1–2 to A.Z., WE1913/11–2) and the Leducq Foundation to C.W.
Weitere Informationen

Publikationsverlauf

Received: 05. September 2011

Accepted after major revision: 06. Februar 2012

Publikationsdatum:
29. November 2017 (online)

Summary

Small non-coding microRNAs (miRNAs) have emerged to play critical roles in cardiovascular biology. Monocytes critically drive atherosclerotic lesion formation, and can be subdivided into a classical and non-classical subset. Here we scrutinised the miRNA signature of human classical and non-classical monocytes, and compared miRNA expression profiles of atherosclerotic plaques from human carotid arteries and healthy arteries. We identified miRNAs to be differentially regulated with a two-fold or higher difference between classical and non-classical monocyte subsets. Moreover, comparing miRNA expression in atherosclerotic plaques compared to healthy arteries, we observed several miRNAs to be aberrantly expressed, with the majority of miRNAs displaying a two-fold or higher increase in plaques and only few miRNAs being decreased. To elucidate similarities in miRNA signatures between monocyte subsets and atherosclerotic plaque, expression of miRNAs highly abundant in monocytes and plaque tissues were compared. Several miRNAs were found in atherosclerotic plaques but not in healthy vessels or either monocyte subset. However, we could identify miRNAs co-expressed in plaque tissue and classical monocytes (miR-99b, miR-152), or non-classical monocytes (miR-422a), or in both monocytes subsets. We thus unravelled candidate miRNAs, which may facilitate our understanding of monocyte recruitment and fate during atherosclerosis, and may serve as therapeutic targets for treating inflammatory vascular diseases.

Note: The editorial process for this article was fully handled by Prof. G. Y. H. Lip, Editor-in-Chief.

These authors contributed equally to this work.


These authors contributed equally to this work.


 
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