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在经SV40的tsA640突变体转化的小鼠巨噬细胞中,T抗原重新表达后诱导纤连蛋白表达、肌动蛋白索形成并进入S期。

Induction of fibronectin expression, actin cable formation, and entry into S phase following reexpression of T antigen in mouse macrophages transformed by the tsA640 mutant of SV40.

作者信息

Takayama H, Tanigawa T, Tanaka Y, Kimura G

出版信息

J Cell Physiol. 1986 Aug;128(2):271-8. doi: 10.1002/jcp.1041280219.

Abstract

Mouse macrophages transformed by a temperature-sensitive mutant (tsA640) of simian virus 40 (SV40) were examined by immunofluorescence microscopy for fibronectin expression and actin distribution. Resting cultures of tsA640 transformants incubated at a temperature nonpermissive for SV40 large T antigen (39.0 degrees C) exhibited phagocytic activity and did not exhibit cellular fibronectin and actin cables, like primary cultures of resident macrophages. When the resting cultures were sparsely seeded and shifted down to the permissive temperature of 33.0 degrees C, expression of large T antigen in the nucleus, expression of fibronectin in the cytoplasm, and cellular entry into S phase occurred in that temporal order, followed by actin cable formation, cellular proliferation, and diminishment of phagocytic activity. The expression of T antigen and fibronectin was sensitive to actinomycin D and cycloheximide. The expression of fibronectin was insensitive to inhibitors of DNA synthesis, whereas the expression of actin cables was sensitive. These results suggest that SV40 T antigen leads macrophages to express fibronectin and actin cables, as well as resumption of cell proliferation, and that entry into S phase is not required for fibronectin expression but may be required for actin cable formation.

摘要

利用免疫荧光显微镜检查法,对被猿猴病毒40(SV40)的温度敏感突变体(tsA640)转化的小鼠巨噬细胞进行纤连蛋白表达和肌动蛋白分布情况的检测。在对SV40大T抗原非允许的温度(39.0摄氏度)下孵育的tsA640转化体静止培养物,表现出吞噬活性,且未呈现细胞纤连蛋白和肌动蛋白束,这与驻留巨噬细胞的原代培养物类似。当将静止培养物稀疏接种并转移至33.0摄氏度的允许温度时,细胞核中大T抗原的表达、细胞质中纤连蛋白的表达以及细胞进入S期按此时间顺序发生,随后是肌动蛋白束形成、细胞增殖以及吞噬活性减弱。T抗原和纤连蛋白的表达对放线菌素D和环己酰亚胺敏感。纤连蛋白的表达对DNA合成抑制剂不敏感,而肌动蛋白束的表达则敏感。这些结果表明,SV40 T抗原促使巨噬细胞表达纤连蛋白和肌动蛋白束,以及恢复细胞增殖,并且进入S期对于纤连蛋白表达并非必需,但可能是肌动蛋白束形成所必需的。

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