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对人脐静脉内皮细胞对某些生长因子反应的重新评估。

A reevaluation of the response of human umbilical vein endothelial cells to certain growth factors.

作者信息

Knauer D J, Cunningham D D

出版信息

J Cell Physiol. 1983 Dec;117(3):397-406. doi: 10.1002/jcp.1041170315.

Abstract

Human umbilical vein endothelial cells (HUV-EC) were isolated and maintained in pure culture on a fibronectin matrix with hypothalamic derived endothelial cell growth factor included in the culture medium. HUV-EC maintained under these conditions displayed only slight alterations in morphological appearance and continued to produce Factor VIII antigen. The cells showed an unaltered growth response to serum and added growth factors up to passage 16 (greater than 30 population doublings). We found that epidermal growth factor (EGF) was potently mitogenic for HUV-EC, but only in the presence of endothelial cell growth factor. Also in contrast to a previous report, we were unable to demonstrate a potentiation of this response by human alpha-thrombin. Because of these discrepancies, we performed studies to determine if they might be explained by a difference in the interaction of our HUV-EC with EGF. In studies utilizing 125I-EGF as tracer probe, we determined that our HUV-EC have an EGF receptor number of 13,000 sites/cell with an apparent Kd-4.0 X 10(-9) M. In addition, receptor-bound 125I-EGF was rapidly internalized and degraded presumably by a lysosomally mediated pathway since degradation was complete to the amino acid level. These results are in agreement with those previously published and thus do not provide a basis on which to resolve discrepancies regarding the growth response of HUV-EC to various growth factors.

摘要

人脐静脉内皮细胞(HUV-EC)被分离出来,并在纤连蛋白基质上进行纯培养,培养基中含有下丘脑衍生的内皮细胞生长因子。在这些条件下培养的HUV-EC在形态外观上仅表现出轻微变化,并继续产生因子VIII抗原。这些细胞在传代16次(超过30次群体倍增)之前,对血清和添加的生长因子显示出未改变的生长反应。我们发现表皮生长因子(EGF)对HUV-EC有强烈的促有丝分裂作用,但仅在内皮细胞生长因子存在的情况下。此外,与之前的一份报告相反,我们无法证明人α-凝血酶能增强这种反应。由于这些差异,我们进行了研究,以确定它们是否可以通过我们的HUV-EC与EGF相互作用的差异来解释。在利用125I-EGF作为示踪探针的研究中,我们确定我们的HUV-EC的EGF受体数量为13,000个位点/细胞,表观解离常数Kd为4.0×10(-9)M。此外,受体结合的125I-EGF迅速被内化并降解,推测是通过溶酶体介导的途径,因为降解完全达到氨基酸水平。这些结果与之前发表的结果一致,因此没有为解决关于HUV-EC对各种生长因子生长反应的差异提供依据。

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