Human tribbles homologue 2 is expressed in unstable regions of carotid plaques and regulates macrophage IL-10 in vitro

Author:

Deng Jingti1,James Christian H.2,Patel Lisa3,Smith Alberto4,Burnand Kevin G.4,Rahmoune Hassan1,Lamb Jonathan R.5,Davis Bill1

Affiliation:

1. GlaxoSmithKline Clinical Unit, Addenbrooke's Centre for Clinical Investigation, Addenbrooke's Hospital, Cambridge CB2 2GG, U.K.

2. Translational and Regenerative Medicine, GlaxoSmithKline, King of Prussia, PA 19406, U.S.A.

3. Department of Atherosclerosis, Medicines Research Centre, GlaxoSmithKline, Stevenage SG1 2NY, U.K.

4. Academic Department of Surgery, Cardiovascular Division, King's College London, St Thomas' Hospital, London SE1 7EH, U.K.

5. Royal (Dick) School of Veterinary Studies, University of Edinburgh, Roslin EH25 9RG, U.K.

Abstract

Mammalian orthologues of the Drosophila tribbles protein (Trb1, Trb2 and Trb3) are a recently described family of signalling molecules that regulate gene expression by modulation of protein kinase signalling pathways. In the present study, a screen for mRNA species specifically regulated in vulnerable regions of human atherosclerotic plaque demonstrated the up-regulation of both Trb1 and Trb2, the latter by more than 8-fold. In vitro experiments in primary human monocyte-derived macrophages showed that Trb2 expression was up-regulated by treatment with oxidized LDL (low-density lipoprotein), and that expression of recombinant Trb2 specifically reduced macrophage levels of IL-10 (interleukin-10) mRNA. Our results thus identify Trb2 as a highly regulated gene in vulnerable atherosclerotic lesions, and demonstrate inhibition of macrophage IL-10 biosynthesis as a potential pro-inflammatory consequence of high Trb2 expression, which may contribute to plaque instability.

Publisher

Portland Press Ltd.

Subject

General Medicine

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