Back to Search
Start Over
G Protein–Coupled Receptors as Potential Drug Targets for Lymphangiogenesis and Lymphatic Vascular Diseases
- Source :
- Arteriosclerosis, Thrombosis, and Vascular Biology. 29:650-656
- Publication Year :
- 2009
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2009.
-
Abstract
- 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.
- Subjects :
- Endothelium
government.form_of_government
Biology
Article
Receptors, G-Protein-Coupled
Mice
medicine
Animals
Humans
Lymphedema
Lymphangiogenesis
Receptor
G protein-coupled receptor
Mice, Knockout
Receptor activity-modifying protein
Calcitonin Receptor-Like Protein
Receptors, Calcitonin
Lymphatic Capillary
Lymphatic Endothelium
Lymphatic system
medicine.anatomical_structure
Receptors, Lysophospholipid
Immunology
Cancer research
government
Endothelium, Lymphatic
Cardiology and Cardiovascular Medicine
Subjects
Details
- ISSN :
- 15244636 and 10795642
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Accession number :
- edsair.doi.dedup.....b9716a2d78dd8209c04ca8c9e29fbddd
- Full Text :
- https://doi.org/10.1161/atvbaha.109.185066