Tasinato A, Boscoboinik D, Bartoli G M, Maroni P, Azzi A
Institut für Biochemie und Molekularbiologie, Universität Bern, Switzerland.
Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12190-4. doi: 10.1073/pnas.92.26.12190.
d-alpha-Tocopherol, but not d-beta-tocopherol, negatively regulates proliferation of vascular smooth muscle cells at physiological concentrations. d-alpha-Tocopherol inhibits protein kinase C (PKC) activity, whereas d-beta-tocopherol is ineffective. Furthermore d-beta-tocopherol prevents the inhibition of cell growth and of PKC activity caused by d-alpha-tocopherol. The negative regulation by d-alpha-tocopherol of PKC activity appears to be the cause and not the effect of smooth muscle cell growth inhibition. d-alpha-Tocopherol does not act by binding to PKC directly but presumably by preventing PKC activation. It is concluded that, in vascular smooth muscle cells, d-alpha-tocopherol acts specifically through a nonantioxidant mechanism and exerts a negative control on a signal transduction pathway regulating cell proliferation.
在生理浓度下,d-α-生育酚而非d-β-生育酚对血管平滑肌细胞的增殖具有负向调节作用。d-α-生育酚可抑制蛋白激酶C(PKC)的活性,而d-β-生育酚则无此作用。此外,d-β-生育酚可阻止d-α-生育酚对细胞生长及PKC活性的抑制。d-α-生育酚对PKC活性的负向调节似乎是平滑肌细胞生长抑制的原因而非结果。d-α-生育酚并非直接通过与PKC结合起作用,推测是通过阻止PKC的激活发挥作用。研究得出结论,在血管平滑肌细胞中,d-α-生育酚通过一种非抗氧化机制特异性发挥作用,并对调节细胞增殖的信号转导通路施加负向调控。