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1型人类免疫缺陷病毒Vpr基因产物可阻止小鼠NIH3T3细胞增殖,而不会使细胞周期停滞于G2期。

Human immunodeficiency virus type 1 Vpr gene product prevents cell proliferation on mouse NIH3T3 cells without the G2 arrest of the cell cycle.

作者信息

Nishino Y, Myojin T, Kamata M, Aida Y

机构信息

Laboratory of Gene Technology and Safety, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.

出版信息

Biochem Biophys Res Commun. 1997 Mar 17;232(2):550-4. doi: 10.1006/bbrc.1997.6186.

Abstract

Human immunodeficiency virus type 1 Vpr is a 96-amino-acid virion-associated protein that arrests cells in the G2 phase of the cell cycle in peripheral blood lymphocytes, HeLa, 293, 293T, A549, Jurkat, CEM, SupT1, CV-1 and COS1 cells. When we transfected Vpr expression vector into mouse NIH3T3 and then cultured it in the presence of G418, NIH3T3 cells were the drug resistant cells yielded. The surviving colonies, however, exhibited a degenerating morphology up to 8 approximately 20-fold smaller than the control vector colonies. In addition, the growth of NIH3T3 cells transiently transfected with Vpr expression vector declined dramatically compared with that of transfectants with control vector, suggesting that Vpr significantly interferes with cell proliferation of NIH3T3 cells. Cell cycle characterization by flow cytometry indicated that expression of Vpr did not induce G2 cessation in NIH3T3. These findings strongly suggest that Vpr has a novel pathway to retard cell growth independently and arrests the G2 phase of the cell cycle.

摘要

人类免疫缺陷病毒1型Vpr是一种由96个氨基酸组成的病毒体相关蛋白,可使外周血淋巴细胞、HeLa细胞、293细胞、293T细胞、A549细胞、Jurkat细胞、CEM细胞、SupT1细胞、CV-1细胞和COS1细胞的细胞周期停滞于G2期。当我们将Vpr表达载体转染到小鼠NIH3T3细胞中,然后在G418存在的情况下进行培养时,得到了耐药的NIH3T3细胞。然而,存活的菌落呈现出退化的形态,比对照载体菌落小约8至20倍。此外,与转染对照载体的细胞相比,瞬时转染Vpr表达载体的NIH3T3细胞的生长显著下降,这表明Vpr显著干扰了NIH3T3细胞的增殖。通过流式细胞术进行的细胞周期特征分析表明,Vpr的表达并未诱导NIH3T3细胞停滞于G2期。这些发现强烈表明,Vpr具有一条独立延缓细胞生长并使细胞周期停滞于G2期的新途径。

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