Details

Autor(en) / Beteiligte

• Guntani, Atsushi, M.D
• Matsumoto, Takuya, M.D., Ph.D
• Kyuragi, Ryoichi, M.D
• Iwasa, Kazuomi, M.D
• Onohara, Toshihiro, M.D., Ph.D
• Itoh, Hiroyuki, M.D., Ph.D
• Katusic, Zvonimir S., M.D., Ph.D
• Maehara, Yoshihiko, M.D., Ph.D

Titel

Reduced Proliferation of Aged Human Vascular Smooth Muscle Cells—Role of Oxygen-Derived Free Radicals and BubR1 Expression

Ist Teil von

• The Journal of surgical research, 2011-09, Vol.170 (1), p.143-149

Ort / Verlag

New York, NY: Elsevier Inc

Erscheinungsjahr

2011

Quelle

MEDLINE

Beschreibungen/Notizen

• Background Aging is a risk factor for atherosclerosis. Recent studies suggest cell cycle events as well as reactive oxygen species (ROS) contribute to vascular cell dysfunction associated with aging. Mice expressing low levels of the spindle assembly checkpoint protein BubR1 develop aging-associated vascular changes at a young age, including decreased smooth muscle cells and increased reactive oxygen species (ROS) production. This study was designed to determine the effect of aging and production of oxygen-derived free radicals on expression of BubR1. Materials and Methods To assess cell proliferation capacity, human aortic smooth muscle cells (hAoSMC) derived from a young group (17-30 y) or an aged group (57-62 y) were cultured, and cell numbers were directly counted in using a Neubauer chamber. RT-PCR assay was used to evaluate BubR1 expression in cultured hAoSMC stimulated with Angiotensin II or H2 O2. Results No significant difference in BubR1 expression or hAoSMC proliferative ability was demonstrated at passage 5, but both were significantly decreased at passage 8 in the aged hAoSMC. Angiotensin II and H2 O2 up-regulated BubR1 expression in young hAoSMC, and the up-regulation was abrogated by a p38 MAPK inhibitor or an inhibitor of the NADH/NADPH oxidase. siRNA against BubR1 reduced proliferative activity and increased ROS production in hAoSMC. Conclusions These findings demonstrate BubR1 mRNA expression decreases along with proliferation in aged hAoSMC. Aging-related loss of BubR1 and subsequent impairment of reactivity to ROS may explain reduced proliferative capacity of aged smooth muscle cells.