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PMID: 16750822 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo.

Developmental biology ·Vol. 296 ·No. 1 ·2006-08-01 ·Pages 177-89

Cox CM, D'Agostino SL, Miller MK, Heimark RL, Krieg PA

Abstract

The peptide growth factor apelin is the high affinity ligand for the G-protein-coupled receptor APJ. During embryonic development of mouse and frog, APJ receptor is expressed at high levels in endothelial precursor cells and in nascent vascular structures. Characterization of Xenopus apelin shows that the sequence of the bioactive region of the peptide is perfectly conserved between frogs and mammals. Embryonic expression studies indicate that apelin is expressed in, or immediately adjacent to, a subset of the developing vascular structures, particularly the intersegmental vessels. Experimental inhibition of either apelin or APJ expression, using antisense morpholino oligos, results in elimination or disruption of intersegmental vessels in a majority of embryos. In gain of function experiments, apelin peptide is a potent angiogenic factor when tested using two in vivo angiogenesis assays, the frog embryo and the chicken chorioallantoic membrane. Furthermore, studies using the mouse brain microvascular cell line bEnd.3 show that apelin acts as a mitogenic, chemotactic and anti-apoptotic agent for endothelial cells in culture. Finally, we show that, similar to a number of other angiogenic factors, expression of the apelin gene is increased under conditions of hypoxia. Taken together, these studies indicate that apelin is required for normal vascular development in the frog embryo and has properties consistent with a role during normal and pathological angiogenesis.

MeSH Terms
Amino Acid Sequence Angiogenesis Inducing Agents/metabolism Animals Embryo, Nonmammalian/blood supply,metabolism,physiology Endothelium, Vascular/embryology,growth & development,metabolism Gene Expression Profiling Intercellular Signaling Peptides and Proteins/metabolism,physiology Molecular Sequence Data Neovascularization, Physiologic Receptors, G-Protein-Coupled/metabolism,physiology Xenopus Xenopus Proteins/metabolism,physiology
Chemicals
APLN protein, Xenopus APLNR protein, Xenopus Angiogenesis Inducing Agents Intercellular Signaling Peptides and Proteins Receptors, G-Protein-Coupled Xenopus Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cox Christopher M
Department of Cell Biology and Anatomy, University of Arizona Health Sciences Center, 1501 N. Campbell Avenue, Tucson, AZ 85724-5044, USA.
D'Agostino Susan L
Miller Melanie K
Heimark Ronald L
Krieg Paul A
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
2006-08-01
Epub
2006-00-27
Pages
177-89
Language
English
Region
United States
NLM ID
0372762
Subset
IM
Grants
NHLBI NIH HHS · HL 63926 · United States
NHLBI NIH HHS · HL 74184 · United States
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