Literature DB >> 23868938

Toll-like receptor 2/6 agonist macrophage-activating lipopeptide-2 promotes reendothelialization and inhibits neointima formation after vascular injury.

Karsten Grote1, Kristina Sonnenschein, Piyushkumar R Kapopara, Anja Hillmer, Christina Grothusen, Gustavo Salguero, Daniel Kotlarz, Harald Schuett, Udo Bavendiek, Bernhard Schieffer.   

Abstract

OBJECTIVE: Reendothelialization after vascular injury (ie, balloon angioplasty or stent implantation) is clinically extremely relevant to promote vascular healing. We here investigated the therapeutic potential of the toll-like receptor 2/6 agonist macrophage-activating lipopeptide (MALP)-2 on reendothelialization and neointima formation in a murine model of vascular injury. APPROACH AND
RESULTS: The left common carotid artery was electrically injured, and reendothelialization was quantified by Evans blue staining after 3 days. A single injection of MALP-2 (1 or 10 µg, IV) after vascular injury accelerated reendothelialization (P<0.001). Proliferation of endothelial cells at the wound margins determined by 5-ethynyl-2'-deoxyuridine incorporation was significantly higher in MALP-2-treated animals (P<0.05). Furthermore, wire injury-induced neointima formation of the left common carotid artery was completely prevented by a single injection of MALP-2 (10 µg, IV). In vitro, MALP-2 induced proliferation (BrdU incorporation) and closure of an artificial wound of endothelial cells (P<0.05) but not of smooth muscle cells. Protein array and ELISA analysis of isolated primary endothelial cells and ex vivo stimulated carotid segments revealed that MALP-2 stimulated the release of multiple growth factors and cytokines predominantly from endothelial cells. MALP-2 induced a strong activation of the mitogen-activated protein kinase cascade in endothelial cells, which was attenuated in smooth muscle cells. Furthermore, MALP-2 significantly enhanced circulating monocytes and hematopoietic progenitor cells.
CONCLUSIONS: The toll-like receptor 2/6 agonist MALP-2 promotes reendothelialization and inhibits neointima formation after experimental vascular injury via enhanced proliferation and migration of endothelial cells. Thus, MALP-2 represents a novel therapeutic option to accelerate reendothelialization after vascular injury.

Entities:  

Keywords:  cytokines; endothelial growth factors; neointima formation; toll-like receptors; vascular system injuries

Mesh:

Substances:

Year:  2013        PMID: 23868938     DOI: 10.1161/ATVBAHA.113.301799

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  5 in total

1.  Antiphospholipid antibodies attenuate endothelial repair and promote neointima formation in mice.

Authors:  Victoria Ulrich; Eddy S Konaniah; Wan-Ru Lee; Sadiksha Khadka; Yu-Min Shen; Joachim Herz; Jane E Salmon; David Y Hui; Philip W Shaul; Chieko Mineo
Journal:  J Am Heart Assoc       Date:  2014-10-14       Impact factor: 5.501

2.  Arterial smooth muscle.

Authors:  Valerie Z Wall; Karin E Bornfeldt
Journal:  Arterioscler Thromb Vasc Biol       Date:  2014-10       Impact factor: 8.311

3.  Co-upregulation of Toll-like receptors 2 and 6 on peripheral blood cells in patients with obstructive sleep apnea.

Authors:  Yung-Che Chen; Mao-Chang Su; Chia-Wei Liou; Shih-Feng Liu; Chung-Jen Chen; Hsin-Ching Lin; Chang-Chun Hsiao; Ting-Ya Wang; Chin-Chou Wang; Chien-Hung Chin; Kuo-Tung Huang; An-Shen Lin; Meng-Chih Lin
Journal:  Sleep Breath       Date:  2015-01-22       Impact factor: 2.816

4.  Notoginsenoside Fc Accelerates Reendothelialization following Vascular Injury in Diabetic Rats by Promoting Endothelial Cell Autophagy.

Authors:  Jingjing Liu; Chunyu Jiang; Xu Ma; Lishuai Feng; Jianbo Wang
Journal:  J Diabetes Res       Date:  2019-09-03       Impact factor: 4.011

5.  The Lipopeptide MALP-2 Promotes Collateral Growth.

Authors:  Kerstin Troidl; Christian Schubert; Ann-Kathrin Vlacil; Ramesh Chennupati; Sören Koch; Jutta Schütt; Raghav Oberoi; Wolfgang Schaper; Thomas Schmitz-Rixen; Bernhard Schieffer; Karsten Grote
Journal:  Cells       Date:  2020-04-16       Impact factor: 6.600

  5 in total

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