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黄曲霉毒素转化的C3H/10T1/2细胞中蛋白激酶C过表达,并且对佛波酯处理的反应发生了改变。

Aflatoxin-transformed C3H/10T1/2 cells overexpress protein kinase C and have an altered response to phorbol ester treatments.

作者信息

Dunn J A, Faletto M B, Kasper S J, Gurtoo H L

机构信息

Life Sciences Research Laboratory, Eastman Kodak Company, Rochester, New York 14650.

出版信息

Cancer Res. 1992 Feb 15;52(4):990-6.

PMID:1737362
Abstract

The aflatoxin B1-transformed C3H/10T1/2 (10T1/2) cell line 7SA has disordered growth in culture and is tumorigenic in syngeneic mice. Chronic exposure (14 days) of 10T1/2 and 7SA cells to phorbol 12,13-dibutyrate (PDBu) increased the saturation density of 10T1/2 cells but dramatically slowed the entry of 7SA cells into the log phase of growth without affecting their final saturation density. Similar PDBu treatment of low-density cultures dramatically decreased the size of 7SA colonies. Both cell lines bound [3H]PDBu in a specific and saturable manner. Analysis of this binding yielded linear Scatchard plots for both cell lines with distinctly different Kd values (10.7 nM for 10T1/2 versus 54.5 nM for 7SA). The total amount of [3H]PDBu bound was 2-fold greater in the 7SA cells versus the 10T1/2 cell line. Both cell lines released arachidonic acid following a 2-h exposure to PDBu; however, the magnitude of the response of the 7SA cells was only one-half that of the 10T1/2 cells. Western blot analysis of protein kinase C (PKC) using specific anti-PKC antibodies revealed a greater total amount of PKC alpha in the 7SA cells relative to an equal number of 10T1/2 cells. No immunoreactive PKC alpha was found in either cell line 16 h after exposure to 600 nM PDBu; however, PKC alpha returned to control levels in both cell lines 24 h after removal of the phorbol ester. These results suggest that an overexpression of PKC alpha may play a role in the altered biological properties of aflatoxin-transformed 10T1/2 cells.

摘要

黄曲霉毒素B1转化的C3H/10T1/2(10T1/2)细胞系7SA在培养中生长紊乱,且在同基因小鼠中具有致瘤性。10T1/2和7SA细胞长期(14天)暴露于佛波醇12,13 - 二丁酸酯(PDBu),增加了10T1/2细胞的饱和密度,但显著减缓了7SA细胞进入对数生长期的速度,且不影响其最终饱和密度。对低密度培养物进行类似的PDBu处理,显著减小了7SA集落的大小。两种细胞系均以特异性和可饱和的方式结合[3H]PDBu。对这种结合的分析得出两种细胞系的线性Scatchard图,其解离常数(Kd)值明显不同(10T1/2为10.7 nM,7SA为54.5 nM)。7SA细胞中结合的[3H]PDBu总量是10T1/2细胞系的2倍。两种细胞系在暴露于PDBu 2小时后均释放花生四烯酸;然而,7SA细胞的反应强度仅为10T1/2细胞的一半。使用特异性抗蛋白激酶C(PKC)抗体对PKC进行蛋白质印迹分析显示,相对于等量的10T1/2细胞,7SA细胞中PKCα的总量更多。在暴露于600 nM PDBu 16小时后,两种细胞系中均未发现免疫反应性PKCα;然而,在去除佛波醇酯24小时后,两种细胞系中的PKCα均恢复到对照水平。这些结果表明,PKCα的过表达可能在黄曲霉毒素转化的10T1/2细胞生物学特性改变中起作用。

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