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一种人类巨核细胞肿瘤细胞系产生生长因子的情况。

Growth factor production by a human megakaryocytic tumor cell line.

作者信息

Witte D P, Stambrook P J, Feliciano E, Jones C L, Lieberman M A

机构信息

Department of Pathology, University of Cincinnati College of Medicine, Ohio 45267-0522.

出版信息

J Cell Physiol. 1988 Oct;137(1):86-94. doi: 10.1002/jcp.1041370110.

Abstract

A recently described human megakaryocytic tumor cell line was analyzed for the presence of growth factor activity and was found to produce large quantities of transforming growth factor beta-like (TGF-beta) and basic fibroblast growth factor-like (bFGF) activities. Growth factor activities were identified using a radioreceptor assay for the TGF-beta-like activity, a heparin-binding assay for the b-FGF-like activity, and a demonstration of distinct biological activities for each type of factor. Tumor poly-A+ RNA revealed strong signals when probed with complementary DNA corresponding to bovine basic FGF and human TGF-beta and weak signals when probed with cDNA corresponding to epidermal growth factor (EGF) and TGF-alpha. The levels of EGF and TGF-alpha produced in the tumor line were too low to be detected by radioreceptor assays. Relative levels of messenger RNA encoding each of the growth factors reflected the relative levels of each of the respective factors tested. These data represent the first definitive identification of FGF-like activities in megakaryocytic-like cell lines. Interestingly, the line displayed little activity similar to platelet-derived growth factor (PDGF) when assayed either biochemically or by poly-A+ RNA analysis.

摘要

对最近描述的一种人巨核细胞肿瘤细胞系进行了生长因子活性检测,发现其产生大量转化生长因子β样(TGF-β)和碱性成纤维细胞生长因子样(bFGF)活性。使用针对TGF-β样活性的放射受体测定法、针对bFGF样活性的肝素结合测定法以及对每种因子独特生物学活性的证明来鉴定生长因子活性。当用对应于牛碱性FGF和人TGF-β的互补DNA进行探测时,肿瘤多聚腺苷酸加尾RNA显示出强信号,而当用对应于表皮生长因子(EGF)和TGF-α的cDNA进行探测时显示出弱信号。肿瘤细胞系中产生的EGF和TGF-α水平过低,无法通过放射受体测定法检测到。编码每种生长因子的信使RNA的相对水平反映了所检测的各自因子的相对水平。这些数据代表了首次在巨核细胞样细胞系中明确鉴定出FGF样活性。有趣的是,当通过生化方法或多聚腺苷酸加尾RNA分析进行检测时,该细胞系显示出与血小板衍生生长因子(PDGF)相似的活性很低。

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