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Arteriosclerosis, Thrombosis, and Vascular Biology
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Arteriosclerosis, Thrombosis, and Vascular Biology. 2009;29:650-656
Published online before print March 5, 2009, doi: 10.1161/ATVBAHA.109.185066
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*Lymphedema
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Right arrow Developmental Biology in the Vasculature
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2009;29:650.)
© 2009 American Heart Association, Inc.


Brief Reviews

G Protein–Coupled Receptors as Potential Drug Targets for Lymphangiogenesis and Lymphatic Vascular Diseases

William P. Dunworth; Kathleen M. Caron

From the Departments of Cell and Molecular Physiology and Genetics, the University of North Carolina at Chapel Hill.

Correspondence to Kathleen M. Caron, 111 Mason Farm Road, 247 Medical Biomolecular Research Bldg, Room 6340B, CB # 7545, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599. E-mail Kathleen_caron{at}med.unc.edu

Series Editor: Mark Majesky PhD

Absrtract— G protein–coupled receptors (GPCRs) are widely expressed cell surface receptors that have been successfully exploited for the treatment of a variety of human diseases. Recent studies in genetically engineered mouse models have led to the identification of several GPCRs important for lymphatic vascular development and function. The adrenomedullin receptor, which consists of an oligomer between calcitonin receptor-like receptor and receptor activity modifying protein 2, is required for normal lymphatic vascular development and regulates lymphatic capillary permeability in mice. Numerous studies also suggest that lysophospholipid receptors are involved in the development of lymphatic vessels and lymphatic endothelial cell permeability. Given our current lack of pharmacological targets for the treatment of lymphatic vascular diseases like lymphedema, the continued identification and study of GPCRs in lymphatic endothelial cells may eventually lead to major breakthroughs and new pharmacological strategies for the treatment of lymphedema.

Recently, several GPCRs important for lymphatic vascular development and function have been identified. Given our current lack of pharmacological targets for the treatment of lymphatic vascular diseases, the continued identification and study of GPCRs in lymphatics may eventually lead to new pharmacological strategies for the treatment of lymphedema.


Key Words: angiogenesis • other treatment • animal models of human disease • endothelium • other vascular biology




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M. W. Majesky
Developmental Biology in the Vasculature--Review Series
Arterioscler Thromb Vasc Biol, May 1, 2009; 29(5): 622 - 622.
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