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血清刺激撤除对培养成纤维细胞蛋白质合成机制的影响。

Effects of withdrawal of a serum stimulus on the protein-synthesizing machinery of cultured fibroblasts.

作者信息

Mostafapour M K, Green H

出版信息

J Cell Physiol. 1975 Oct;86(2 PT 2 SUPPL 1):313-9. doi: 10.1002/jcp.1040860402.

Abstract

3T6 cells resting in medium containing 0.5% serum were stimulated to prepare for multiplication by the addition of medium containing 10% serum. After a number of hours, when the rate of preribosomal RNA synthesis, total RNA content (mainly ribosomal), and the cytoplasmic content of poly A (a measure of poly A(+) mRNA) were considerably elevated, the serum-rich medium was withdrawn, and the original medium replaced. The rate of preribosomal RNA synthesis began to drop within 30 minutes, but required a much longer time to fall to a new resting level. When the serum-rich medium was withdrawn after 12 hours of stimulation, the total RNA content required 12-18 hours to fall to the resting level, whereas cytoplasmic poly A content and the rate of protein synthesis declined more rapidly, reaching a new resting level within eight hours. During the 12 hours following withdrawal of the serum-rich medium an appreciable fraction of the cells initiated DNA synthesis. Presumably, the cellular preparations for DNA synthesis cannot be immediately reversed because of the inertial factors related to the protein-synthesizing machinery.

摘要

将处于含0.5%血清培养基中的3T6细胞,通过添加含10%血清的培养基来刺激其为增殖做准备。数小时后,当核糖体前体RNA合成速率、总RNA含量(主要是核糖体RNA)以及多聚A的细胞质含量(多聚A(+) mRNA的一个指标)显著升高时,撤去富含血清的培养基,并用原来的培养基替换。核糖体前体RNA合成速率在30分钟内开始下降,但需要更长时间才能降至新的静止水平。在刺激12小时后撤去富含血清的培养基时,总RNA含量需要12 - 18小时才能降至静止水平,而细胞质多聚A含量和蛋白质合成速率下降得更快,在8小时内达到新的静止水平。在撤去富含血清的培养基后的12小时内,相当一部分细胞开始进行DNA合成。据推测,由于与蛋白质合成机制相关的惯性因素,细胞对DNA合成的准备不能立即逆转。

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