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1α,25-二羟基维生素D3与地塞米松在诱导小鼠髓系白血病细胞分化中的协同作用。

Cooperative effect of 1 alpha,25-dihydroxyvitamin D3 and dexamethasone in inducing differentiation of mouse myeloid leukemia cells.

作者信息

Miyaura C, Abe E, Honma Y, Hozumi M, Nishii Y, Suda T

出版信息

Arch Biochem Biophys. 1983 Dec;227(2):379-85. doi: 10.1016/0003-9861(83)90467-8.

Abstract

Murine myeloid leukemia cells (MI) are induced to differentiate into macrophages by the metabolically active form of vitamin D3,1 alpha,25-dihydroxyvitamin D3[1 alpha,25(OH)2D3] (E. Abe et al., (1981) Proc. Natl. Acad. Sci. USA 78, 4990-4994). At 0.12-120 nM, 1 alpha,25(OH)2D3 suppressed cell growth in a dose-dependent manner and markedly induced phagocytic activity, lysozyme activity, and C3-receptor formation. The potency of 1 alpha,25(OH)2D3, at 0.12-120 nM, in inducing differentiation was nearly equivalent to that of 10-10,000 nM of dexamethasone, one of the most potent stimulators of Ml cells. Simultaneous treatment with low physiological plasma concentrations of 1 alpha,25(OH)2D3 (0.12 nM) and dexamethasone (10 nM) induced differentiation of Ml cells equivalent to the responses obtained only by using much higher concentrations of the respective steroids when used separately. In addition, two variant clones of Ml cells resistant to either 1 alpha,25(OH)2D3 or dexamethasone were isolated. One was resistant to 120 nM of 1 alpha,25(OH)2D3 but sensitive to 10-1000 nM of dexamethasone. The other was resistant to 1000 nM of dexamethasone but sensitive to 12 nM of 1 alpha,25(OH)2D3. This suggests that the mechanism of action of 1 alpha,25(OH)2D3 in inducing differentiation of Ml cells is different at least in part from that of dexamethasone, and that combination therapy by both steroids may be useful in reducing leukemogenicity of Ml cells in vivo.

摘要

维生素D3的代谢活性形式1α,25 - 二羟基维生素D3[1α,25(OH)2D3]可诱导小鼠髓系白血病细胞(MI)分化为巨噬细胞(E. Abe等人,(1981年)《美国国家科学院院刊》78, 4990 - 4994)。在0.12 - 120 nM浓度下,1α,25(OH)2D3以剂量依赖方式抑制细胞生长,并显著诱导吞噬活性、溶菌酶活性和C3受体形成。在0.12 - 120 nM浓度下,1α,25(OH)2D3诱导分化的效力与10 - 10000 nM地塞米松(MI细胞最有效的刺激剂之一)的效力几乎相当。用低生理血浆浓度的1α,25(OH)2D3(0.12 nM)和地塞米松(10 nM)同时处理,诱导MI细胞分化的效果等同于单独使用各自更高浓度类固醇时获得的反应。此外,还分离出了对1α,25(OH)2D3或地塞米松耐药的两个MI细胞变异克隆。一个对120 nM的1α,25(OH)2D3耐药,但对10 - 1000 nM的地塞米松敏感。另一个对1000 nM的地塞米松耐药,但对12 nM的1α,25(OH)2D3敏感。这表明1α,25(OH)2D3诱导MI细胞分化的作用机制至少部分不同于地塞米松,并且两种类固醇联合治疗可能有助于降低MI细胞在体内的致白血病性。

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