Scarpa S, Strom R, Bozzi A, Aksamit R R, Backlund P S, Chen J, Cantoni G L
Proc Natl Acad Sci U S A. 1984 May;81(10):3064-8. doi: 10.1073/pnas.81.10.3064.
Treatment of myoblast cell lines with 3-deazaadenosine stimulates differentiation into myofibers. Myoblast clone L5/ 3B5 , which does not form myofibers after 6 days in fusion medium, was stimulated to form myofibers after 5 days of culture in fusion medium containing 50 microM 3-deazaadenosine. Myoblast clone L5/ 3C4 , which normally begins to form myofibers after 4 days in fusion medium, was stimulated by 50 microM 3-deazaadenosine to form myofibers after 3 days in culture and the extent of fusion was also increased. In the presence of 100 microM homocysteine thiolactone, the concentration of 3-deazaadenosine that stimulated maximal fusion was reduced by a factor of 10, from 50 microM to 5 microM 3-deazaadenosine. Stimulation of myofiber formation by 3-deazaadenosine suggests a requirement for one or more methylation reactions in myoblast differentiation and the potentiation by homocysteine thiolactone indicates that myofiber formation is specifically stimulated by an intracellular accumulation of 3-deazaadenosylhomocysteine.
用3-去氮腺苷处理成肌细胞系可刺激其分化为肌纤维。成肌细胞克隆L5/3B5在融合培养基中培养6天后不形成肌纤维,但在含有50微摩尔3-去氮腺苷的融合培养基中培养5天后,被刺激形成了肌纤维。成肌细胞克隆L5/3C4在融合培养基中正常情况下培养4天后开始形成肌纤维,在50微摩尔3-去氮腺苷的作用下,培养3天后被刺激形成肌纤维,且融合程度也增加了。在存在100微摩尔同型半胱氨酸硫内酯的情况下,刺激最大融合的3-去氮腺苷浓度降低了10倍,从50微摩尔降至5微摩尔3-去氮腺苷。3-去氮腺苷对肌纤维形成的刺激表明成肌细胞分化需要一种或多种甲基化反应,而同型半胱氨酸硫内酯的增强作用表明肌纤维形成是由细胞内3-去氮腺苷同型半胱氨酸的积累特异性刺激的。