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通过选择性内源性抑制剂控制集落形成单位 - 细胞(CFUc)的增殖

Control of CFUc proliferation by selective endogenous inhibitors.

作者信息

Balázs A, Barabás K

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1979 Oct;31(2):125-34. doi: 10.1007/BF02889930.

Abstract

The susceptibility of mouse bone marrow colony forming cells (CFUc) to three different types of proliferation inhibitors in capillary semisolid agar gel was studied. GI-3, a target specific peptide containing granulocyte fraction, T4-1, an oligospecific thymic factor of proteid nature, and the alkylating cytostatics dianhydrogalactitol (DAD) inhibit myeloid colony formation as a function of concentration. The respective MED values amount to 8, 10, and 0.002 microgram/ml. When compared with this same parameter 3H-TdR incorporation into DNA of liquid bone marrow cultures showed a single fold charge for the endogenous inhibitors (GI-3, T4-1) for the cytostatic (DAD) a 3 to 4 fold lower difference. It was demonstrated, that in competitive antagonism of GI-3 and colony stimulating factor the inhibitor prevails over CSF.

摘要

研究了小鼠骨髓集落形成细胞(CFUc)在毛细管半固体琼脂凝胶中对三种不同类型增殖抑制剂的敏感性。GI-3是一种含粒细胞部分的靶向特异性肽,T4-1是一种蛋白质性质的寡特异性胸腺因子,烷基化细胞抑制剂双脱水半乳糖醇(DAD)根据浓度抑制髓系集落形成。各自的半数有效剂量值分别为8、10和0.002微克/毫升。与相同参数相比,将3H-胸苷掺入液体骨髓培养物的DNA中显示,内源性抑制剂(GI-3、T4-1)的变化为1倍,而细胞抑制剂(DAD)的差异则低3至4倍。结果表明,在GI-3与集落刺激因子的竞争性拮抗中,抑制剂胜过集落刺激因子。

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