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向3T3细胞显微注射针对蛋白p53的单克隆抗体可抑制血清诱导的DNA合成。

Microinjection of monoclonal antibody to protein p53 inhibits serum-induced DNA synthesis in 3T3 cells.

作者信息

Mercer W E, Nelson D, DeLeo A B, Old L J, Baserga R

出版信息

Proc Natl Acad Sci U S A. 1982 Oct;79(20):6309-12. doi: 10.1073/pnas.79.20.6309.

Abstract

Monoclonal antibody directed against the transformation-related protein p53 was microinjected manually into the nuclei of quiescent Swiss 3T3 mouse cells. The cells were subsequently stimulated with 10% fetal calf serum. Microinjection of p53 antibody at or around the time of serum stimulation clearly inhibited the subsequent entry of Swiss 3T3 cells into the S phase of the cell cycle. p53 antibody had no effect on serum-stimulated DNA synthesis when it was microinjected 4 hr or later after serum stimulation. Monoclonal antibody to an unrelated antigen, Lyt-2.2, had no effect on serum-stimulated DNA synthesis regardless of the time it was microinjected. Under similar experimental conditions, p53 antibody had no effect on simian virus 40- or adenovirus 2-induced DNA synthesis. These experiments add strength to the suggestion that p53 is involved in the regulation of cell proliferation.

摘要

将针对转化相关蛋白p53的单克隆抗体手动显微注射到静止的瑞士3T3小鼠细胞的细胞核中。随后用10%胎牛血清刺激这些细胞。在血清刺激时或前后显微注射p53抗体明显抑制了瑞士3T3细胞随后进入细胞周期的S期。当在血清刺激4小时或更晚后显微注射p53抗体时,其对血清刺激的DNA合成没有影响。针对无关抗原Lyt-2.2的单克隆抗体,无论显微注射时间如何,对血清刺激的DNA合成均无影响。在类似的实验条件下,p53抗体对猿猴病毒40或腺病毒2诱导的DNA合成没有影响。这些实验进一步证明了p53参与细胞增殖调控的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cb/347110/5d20c7cdba8b/pnas00459-0204-a.jpg

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