Document Detail


Blood is thicker than lymph.
MedLine Citation:
PMID:  18097477     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Growth of blood and lymphatic vessels is essential in the developing embryo and in the pathogenesis of human diseases such as cancer, but the signaling pathways that regulate vessel growth and function are not yet well characterized. In this issue of the JCI, studies by Fritz-Six et al. and Ichikawa-Shindo et al. demonstrate that loss of signaling by the adrenomedullin peptide results in embryonic edema and death (see the related articles beginning on pages 40 and 29, respectively). Remarkably, this phenotype is attributed to defects in lymphatic vessels by one group and to defects in blood vessels by the other. In addition to defining what I believe to be a novel angiogenic signaling pathway, these studies demonstrate the intricate molecular, genetic, and physiologic relationships between blood and lymphatic vessels that must be considered by investigators of vascular biology.
Authors:
Mark L Kahn
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Publication Detail:
Type:  Comment; Journal Article    
Journal Detail:
Title:  The Journal of clinical investigation     Volume:  118     ISSN:  0021-9738     ISO Abbreviation:  J. Clin. Invest.     Publication Date:  2008 Jan 
Date Detail:
Created Date:  2008-01-03     Completed Date:  2008-04-14     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  7802877     Medline TA:  J Clin Invest     Country:  United States    
Other Details:
Languages:  eng     Pagination:  23-6     Citation Subset:  AIM; IM    
Affiliation:
Department of Medicine and University of Pennsylvania Cardiovascular Institute, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. markkahn@mail.med.upenn.edu
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MeSH Terms
Descriptor/Qualifier:
Adrenomedullin / genetics,  metabolism*
Animals
Arteries / metabolism,  pathology
Capillary Permeability / physiology*
Cardiovascular Diseases / genetics,  metabolism,  pathology
Cells, Cultured
Edema / genetics,  metabolism,  pathology
Embryo Loss / genetics,  metabolism,  pathology
Embryonic Stem Cells / metabolism,  pathology
Endothelium, Vascular / metabolism,  pathology
Female
Homeostasis / physiology*
Humans
Intracellular Signaling Peptides and Proteins / genetics
Male
Membrane Proteins / biosynthesis*,  genetics
Mice
Mice, Knockout
Neovascularization, Physiologic / physiology*
Pregnancy
Receptors, Calcitonin / genetics,  metabolism
Receptors, Peptide / genetics,  metabolism*
Tight Junctions / genetics,  metabolism,  pathology
Chemical
Reg. No./Substance:
0/Intracellular Signaling Peptides and Proteins; 0/Membrane Proteins; 0/Receptors, Calcitonin; 0/Receptors, Peptide; 0/adrenomedullin receptor; 0/calcitonin receptor-like receptor; 0/receptor-activity-modifying protein; 148498-78-6/Adrenomedullin
Comments/Corrections
Comment On:
J Clin Invest. 2008 Jan;118(1):40-50   [PMID:  18097475 ]
J Clin Invest. 2008 Jan;118(1):29-39   [PMID:  18097473 ]

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