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在肿瘤形成过程中,7,12-二甲基苯并(a)蒽预先暴露的大鼠气管上皮细胞中的己糖摄取情况。

Hexose uptake in 7,12-dimethylbenz(a)anthracene-preexposed rat tracheal epithelial cells during the progression of neoplasia.

作者信息

Wasilenko W J, Marchok A C

出版信息

Cancer Res. 1984 Jul;44(7):3081-9.

PMID:6426790
Abstract

Hexose uptake during the progression of neoplasia in rat tracheal epithelial cells was studied by measuring the uptake of 2-deoxy[3H]glucose (2-dGlc) in nontumorigenic (C-18) and tumorigenic (T-8, 1000-WT) rat tracheal epithelial cell lines with varying degrees of cell association as well as in: normal primary cell cultures (NPC) derived from explants of nonexposed tracheas; selected primary cell cultures (SPC) generated from explants of 7,12-dimethylbenz(a)anthracene-treated tracheal implants; and primary tumor cell cultures (TPC) derived from explants of 7,12-dimethylbenz(a)anthracene-induced tracheal carcinomas. The latter two groups represented cells from earlier and late stages in the progression of neoplasia, respectively, and each displayed an in vitro growth advantage that allowed for their survival and growth in medium devoid of supplements of pyruvate and insulin. This property was used in this study to select the carcinogen-altered cells from neighboring normal cells. Uptake of 2-dGlc per microgram of DNA was similar in subconfluent cultures of all cell lines. At confluency, uptake per microgram of DNA was reduced markedly (greater than 3-fold) in C-18 cells but it was reduced only 1.3-fold in T-8 cells and 1.6-fold in 1000-WT cells. Hexose uptake was further reduced in T-8 and 1000-WT cell cultures generated as outgrowths from explants of denuded tracheas bearing a reestablished epithelium from each cell line. Under these conditions, T-8 cells retained higher 2-dGlc uptake than did C-18, but uptake by 1000-WT was lower, indicating that tissue-like cell associations have a profound effect on hexose uptake in these epithelial cells. Results were generally similar when uptake was expressed per mg of protein although, in several instances, the interpretation of uptake data was affected by differences in the protein content between cultures (assessed by comparing protein:DNA ratios). Compared to NPC, hexose uptake was lower in SPC and one group of TPC. A second group of TPC, characterized by loose cell associations and much cell overlapping, had distinctly higher 2-dGlc uptake than did controls. Comparable results in these primary cultures were also observed when the number of cells per culture was used as a reference for 2-dGlc uptake. Under conditions of glucose deprivation, hexose uptake was increased in NPC and SPC. The production of lactic acid in each type of culture was dependent on the level of glucose in the medium, and this was nearly 2-fold greater in NPC than in SPC.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

通过测量非致瘤性(C-18)和致瘤性(T-8、1000-WT)大鼠气管上皮细胞系中2-脱氧[³H]葡萄糖(2-dGlc)的摄取,研究了大鼠气管上皮细胞肿瘤形成过程中的己糖摄取情况,这些细胞系具有不同程度的细胞黏附,同时还研究了以下细胞:源自未暴露气管外植体的正常原代细胞培养物(NPC);由7,12-二甲基苯并(a)蒽处理的气管植入物外植体产生的选定原代细胞培养物(SPC);以及源自7,12-二甲基苯并(a)蒽诱导的气管癌外植体的原发性肿瘤细胞培养物(TPC)。后两组分别代表肿瘤形成过程中早期和晚期的细胞,并且每组都表现出体外生长优势,使其能够在缺乏丙酮酸和胰岛素补充剂的培养基中存活和生长。本研究利用这一特性从相邻的正常细胞中筛选出致癌物改变的细胞。所有细胞系亚汇合培养物中每微克DNA的2-dGlc摄取相似。汇合时,C-18细胞中每微克DNA的摄取量显著降低(超过3倍),但T-8细胞中仅降低1.3倍,1000-WT细胞中降低1.6倍。从带有每种细胞系重新建立上皮的剥脱气管外植体生长出的T-8和1000-WT细胞培养物中,己糖摄取进一步降低。在这些条件下,T-8细胞的2-dGlc摄取量高于C-18细胞,但1000-WT细胞的摄取量较低,表明组织样细胞黏附对这些上皮细胞的己糖摄取有深远影响。当以每毫克蛋白质表示摄取量时,结果通常相似,尽管在某些情况下,摄取数据的解释受到培养物之间蛋白质含量差异的影响(通过比较蛋白质与DNA比率评估)。与NPC相比,SPC和一组TPC中的己糖摄取较低。另一组TPC,其特征是细胞黏附松散且细胞大量重叠,其2-dGlc摄取明显高于对照组。当以每个培养物中的细胞数量作为2-dGlc摄取的参考时,在这些原代培养物中也观察到了类似的结果。在葡萄糖缺乏的条件下,NPC和SPC中的己糖摄取增加。每种培养物中乳酸的产生取决于培养基中葡萄糖的水平,NPC中的乳酸产生量几乎是SPC中的2倍。(摘要截断于400字)

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