Thromb Haemost 2014; 112(02): 379-389
DOI: 10.1160/TH13-08-0653
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

Interruption of classic CD40L-CD40 signalling but not of the novel CD40L-Mac-1 interaction limits arterial neointima formation in mice

Florian Willecke§
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Shilpa Tiwari§
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Benjamin Rupprecht
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Dennis Wolf
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Sonja Hergeth
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Natalie Hoppe
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Bianca Dufner
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Lisa Schulte
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Nathaly Anto Michel
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Nora Bukosza
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Timoteo Marchini
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Markus Jäckel
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Peter Stachon
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Ingo Hilgendorf
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Katharina Zeschky
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Rebecca Schleicher
2   Department of Cardiovascular Medicine, University of Tübingen, Tübingen, Germany
,
Harald F. Langer
2   Department of Cardiovascular Medicine, University of Tübingen, Tübingen, Germany
,
Constantin von zur Muhlen
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Christoph Bode
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
,
Karlheinz Peter
3   Baker IDI Heart and Diabetes Institute, Melbourne, Australia
,
Andreas Zirlik
1   Atherogenesis Research Group, Heart Center Freiburg University, Freiburg, Germany
› Author Affiliations
Further Information

Publication History

Received: 12 August 2013

Accepted after major revision: 26 February 2014

Publication Date:
21 November 2017 (online)

Summary

The co-stimulatory immune molecule CD40L figures prominently in a variety of inflammatory conditions including arterial disease. Recently, we made the surprising finding that CD40L mediates atherogenesis independently of its classic receptor CD40 via a novel interaction with the leukocyte integrin Mac-1. Here, we hypothesised that selective blockade of the CD40L-Mac-1 interaction may also retard restenosis. We induced neointima formation in C57/BL6 mice by ligation of the left carotid artery. Mice were randomised to daily intraperitoneal injections of either cM7, a small peptide selectively inhibiting the CD40L-Mac-1 interaction, scM7, a scrambled control peptide, or saline for 28 days. Interestingly, cM7-treated mice developed neointima of similar size compared with mice receiving the control peptide or saline as assessed by computer-assisted analysis of histological cross sections. These data demonstrate that the CD40L-Mac-1 interaction is not required for the development of restenosis. In contrast, CD40-deficient mice subjected to carotid ligation in parallel, developed significantly reduced neointimal lesions compared with respective wild-type controls (2872 ± 843 µm² vs 35469 ± 11870 µm²). Flow cytometry in CD40-deficient mice revealed reduced formation of platelet-granulocyte and platelet-inflammatory monocyte-aggregates. In vitro, supernatants of CD40-deficient platelet-leukocyte aggregates attenuated proliferation and increased apoptosis of smooth muscle cells. Unlike in the setting of atherosclerosis, CD40L mediates neointima formation via its classic receptor CD40 rather than via its recently described novel interaction with Mac-1. Therefore, selective targeting of CD40L-Mac-1 binding does not appear to be a favorable strategy to fight restenosis.

§ These authors contributed equally to this work.


 
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