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纯化的质膜可抑制亚汇合状态的3T3细胞中多肽生长因子诱导的DNA合成。

Purified plasma membranes inhibit polypeptide growth factor-induced DNA synthesis in subconfluent 3T3 cells.

作者信息

Vale R D, Peterson S W, Matiuck N V, Fox C F

出版信息

J Cell Biol. 1984 Mar;98(3):1129-32. doi: 10.1083/jcb.98.3.1129.

Abstract

Plasma membranes derived from NR-6 cells, a variant line of Swiss mouse 3T3 cells that does not have cell surface receptors for epidermal growth factor (EGF), inhibited EGF-induced stimulation of DNA synthesis by 50% in serum-starved, subconfluent 3T3 cells. Membranes derived from SV3T3 cells were much less effective in inhibiting EGF-induced DNA synthesis. This inhibition on DNA synthesis by NR-6 membranes was not a direct effect of membranes on EGF, nor could it be overcome by high concentrations of EGF. NR-6 membranes were most effective when added 3 h before EGF addition and had little effect when added 2 h or more after EGF. NR-6 membranes also reduced the stimulation of DNA synthesis induced by platelet-derived growth factor or fibroblast growth factor in serum-starved 3T3 cells. These findings indicate that membrane-membrane interactions between nontransformed cells may diminish their ability to proliferate in response to serum polypeptide growth factors.

摘要

NR-6细胞源自瑞士小鼠3T3细胞的一个变体株系,该细胞没有表皮生长因子(EGF)的细胞表面受体,其来源的质膜在血清饥饿、未汇合的3T3细胞中,能将EGF诱导的DNA合成刺激抑制50%。源自SV3T3细胞的质膜在抑制EGF诱导的DNA合成方面效果要差得多。NR-6质膜对DNA合成的这种抑制作用并非质膜对EGF的直接作用,高浓度的EGF也无法克服这种抑制。在添加EGF前3小时添加NR-6质膜时效果最佳,在添加EGF后2小时或更长时间添加则几乎没有效果。NR-6质膜还能减少血清饥饿的3T3细胞中血小板衍生生长因子或成纤维细胞生长因子诱导的DNA合成刺激。这些发现表明,未转化细胞之间的膜-膜相互作用可能会削弱它们响应血清多肽生长因子而增殖的能力。

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Conditions determining initiation of DNA synthesis in 3T3 cells.决定3T3细胞中DNA合成起始的条件。
Proc Natl Acad Sci U S A. 1970 May;66(1):204-10. doi: 10.1073/pnas.66.1.204.
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"Contact inhibition" of cell division in 3T3 cells.3T3细胞中细胞分裂的“接触抑制”
Proc Natl Acad Sci U S A. 1968 May;60(1):300-4. doi: 10.1073/pnas.60.1.300.

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