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培养的正常人乳腺上皮细胞中与DNA合成相关的p53核排除

DNA synthesis-associated nuclear exclusion of p53 in normal human breast epithelial cells in culture.

作者信息

Takahashi K, Suzuki K

机构信息

Department of Biochemistry, Kanagawa Cancer Center Research Institute, Yokohama, Japan.

出版信息

Oncogene. 1994 Jan;9(1):183-8.

PMID:8302577
Abstract

Immunohistochemical staining using three monoclonal antibodies to p53 revealed that most normal human breast epithelial cells (HBEC) in the exponential growth phase, have p53 located in the nucleus but that some cells have the protein in the cytoplasm. Cytoplasmic staining of p53 with the monoclonal antibody PAb240 was inhibited by the specific oligopeptide, NTFRHSVVVP, that corresponds to the amino acids between 210 and 219 in p53 and which includes the epitope domain for PAb240. It was not inhibited by the control oligopeptide SPFVTVHNVR. Growth arrest of HBEC achieved by EGF depletion resulted in predominant nuclear location of p53 and stimulation of arrested cells with EGF induced transient nuclear exclusion of the protein when the induced DNA synthesis level was maximal. These observations suggest that p53 in normal HBEC becomes inactivated by nuclear exclusion during cellular DNA synthesis.

摘要

使用三种针对p53的单克隆抗体进行免疫组织化学染色显示,处于指数生长期的大多数正常人乳腺上皮细胞(HBEC)中,p53定位于细胞核,但有些细胞的该蛋白位于细胞质中。单克隆抗体PAb240对p53的细胞质染色被特定的寡肽NTFRHSVVVP抑制,该寡肽对应于p53中210至219位氨基酸,包括PAb240的表位结构域。它不受对照寡肽SPFVTVHNVR的抑制。通过耗尽表皮生长因子(EGF)实现的HBEC生长停滞导致p53主要定位于细胞核,当诱导的DNA合成水平达到最大值时,用EGF刺激停滞细胞会诱导该蛋白短暂地排出细胞核。这些观察结果表明,正常HBEC中的p53在细胞DNA合成过程中通过核排出而失活。

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