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内源性粒细胞抑制剂对细胞增殖的调节作用。

Modulative effect of endogenous granuloid inhibitors on cell proliferation.

作者信息

Balázs A, Klupp T, Zsila G, Blazsek I, Holczinger L, Gaál D

出版信息

Mech Ageing Dev. 1977 May-Jun;6(3):207-18. doi: 10.1016/0047-6374(77)90022-7.

Abstract

The particle-free crude extract of differentiated granulocytes (GCE) and the GI-1, GI-2, GI-3 proliferation inhibitory fractions (M.W. larger than or equal to 70,000 approximately 11,500 and less than or equal to 4000) were studied for the effects they exert on cultured cells. As shown by the curve, in bone marrow suspension cultures, in the dose range of 0.01-10.0 microng/ml, GCE maximally inhibits 3H-TdR incorporation into the DNA for 5.5 hours. In agar-gel cultures, 1.0-5.0 microng/ml of GCE reduces both the number (by 50.6-54.8%) and the size of the colonies formed. The manifestation of the inhibitory effect of GI-1, GI-2 and GI-3 fractions requires 2.5-3.5 hours. The inhibitors designated GI-2 and GI-2 are target-cell specific but they do not reduce 3H-TdR incorporation either in thymocyte suspension or HeLa monolayer cultures. On the other hand GI-1 inhibis the proliferation in HeLa cultures, as well. These endogenous inhibitors exert their optimum effect, even in a partially purified state at 2-4 orders or magnitude lower concentrations than does 1,2/5,6-dianhydrogalactitol (DAD), a cell-aspecific inhibitor used for comparison in the same system.

摘要

研究了分化粒细胞的无颗粒粗提物(GCE)以及GI-1、GI-2、GI-3增殖抑制组分(分子量大于或等于70,000、约11,500以及小于或等于4000)对培养细胞的作用。如图曲线所示,在骨髓悬浮培养中,在0.01 - 10.0微克/毫升的剂量范围内,GCE在5.5小时内最大程度地抑制3H - TdR掺入DNA。在琼脂凝胶培养中,1.0 - 5.0微克/毫升的GCE可减少形成的集落数量(减少50.6 - 54.8%)和集落大小。GI-1、GI-2和GI-3组分的抑制作用在2.5 - 3.5小时后显现。名为GI-2和GI-2的抑制剂具有靶细胞特异性,但它们在胸腺细胞悬浮培养或HeLa单层培养中均不减少3H - TdR掺入。另一方面,GI-1也抑制HeLa培养中的增殖。这些内源性抑制剂即使处于部分纯化状态,在比用于同一系统中作为对照的细胞非特异性抑制剂1,2/5,6 - 脱水半乳糖醇(DAD)低2 - 4个数量级的浓度下也能发挥最佳作用。

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