Journal article
Aging, oxidative responses, and proliferative capacity in cultured mouse aortic smooth muscle cells
Abstract
The cellular mechanisms that contribute to the acceleration of atherosclerosis in aging populations are poorly understood, although it is hypothesized that changes in the proliferative capacity of vascular smooth muscle cells is contributory. We addressed the relationship among aging, generation of reactive oxygen species (ROS), and proliferation in primary culture smooth muscle cells (SMC) derived from the aortas of young (4 mo old) and aged …
Authors
Moon S-K; Thompson LJ; Madamanchi N; Ballinger S; Papaconstantinou J; Horaist C; Runge MS; Patterson C
Journal
AJP Heart and Circulatory Physiology, Vol. 280, No. 6, pp. h2779–h2788
Publisher
American Physiological Society
Publication Date
June 1, 2001
DOI
10.1152/ajpheart.2001.280.6.h2779
ISSN
0363-6135
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AgingAnimalsAortaCell Cycle ProteinsCell DivisionCells, CulturedCyclin D1Cyclin-Dependent Kinase Inhibitor p27DNA DamageDNA, MitochondrialGlutathioneHydrogen PeroxideMaleMiceMicrotubule-Associated ProteinsMitogen-Activated Protein KinasesMitosisModels, CardiovascularMuscle, Smooth, VascularOxidation-ReductionPolymerase Chain ReactionReactive Oxygen SpeciesSuperoxide DismutaseTumor Suppressor Proteins