Abstract
Age-related changes in NPY-driven angiogenesis were investigated using Matrigel and aortic sprouting assays in young (2 months.) and aged (18 months.) mice. In both assays, NPY-induced vessel growth decreased significantly with age. In parallel, aged mice showed reduced expression (RT-PCR) of Y2 receptors and the NPY converting enzyme, dipeptidyl peptidase IV (DPPIV), in spleens. Aging of human microvascular endothelial cells in vitro led to a loss of their mitogenic responses to NPY accompanied by a lack of NPY receptor mRNAs. Thus, NPY-dependent angiogenesis is impaired with age, which is associated with a decreased expression of endothelial NPY receptors (Y2) and DPPIV.
MeSH terms
-
Aging*
-
Animals
-
Aorta / metabolism
-
Cell Division
-
Cells, Cultured
-
Collagen / chemistry
-
Collagen / pharmacology
-
DNA / biosynthesis
-
Dipeptidyl Peptidase 4 / biosynthesis
-
Dose-Response Relationship, Drug
-
Down-Regulation
-
Drug Combinations
-
Endothelium, Vascular / cytology
-
Humans
-
Laminin / chemistry
-
Laminin / pharmacology
-
Mice
-
Mice, Inbred BALB C
-
Microcirculation / metabolism
-
Neovascularization, Physiologic*
-
Neuropeptide Y / pharmacology*
-
Proteoglycans / chemistry
-
Proteoglycans / pharmacology
-
RNA, Messenger / metabolism
-
Receptors, Neuropeptide Y / biosynthesis
-
Reverse Transcriptase Polymerase Chain Reaction
-
Spleen / metabolism
-
Time Factors
Substances
-
Drug Combinations
-
Laminin
-
Neuropeptide Y
-
Proteoglycans
-
RNA, Messenger
-
Receptors, Neuropeptide Y
-
neuropeptide Y2 receptor
-
matrigel
-
Collagen
-
DNA
-
Dipeptidyl Peptidase 4