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非洲绿猴(BSC-1)细胞的生长抑制剂是转化生长因子β1和β2。

The growth inhibitor of African green monkey (BSC-1) cells is transforming growth factors beta 1 and beta 2.

作者信息

McPherson J M, Sawamura S J, Ogawa Y, Dineley K, Carrillo P, Piez K A

机构信息

Celtrix Laboratories, Collagen Corporation, Palo Alto, California 94303.

出版信息

Biochemistry. 1989 Apr 18;28(8):3442-7. doi: 10.1021/bi00434a044.

Abstract

The growth inhibitory activity in conditioned medium of African green monkey kidney epithelial (BSC-1) cells that has been shown to arise, at least in part, from transforming growth factor beta 2 (TGF-beta 2) [Hanks, S. K., Armour, R., Baldwin, J. H., Maldonado, F., Spiess, J., & Holley, R. W. (1988) Proc. Natl. Acad. Sci. U.S.A. 85, 79-82] was tested for growth inhibitory activity prior to and following acidification. Similar to TGF-beta 1 from human platelets, the inhibitory activity from BSC-1 cells demonstrated an 8-10-fold stimulation following acidification, showing that the activity was secreted from the cells in latent form. Conditioned medium from BSC-1 cells was collected, acidified, and fractionated by procedures that separate TGF-beta 1 and -2. Biological activity was assayed by using the BSC-1 cell proliferation assay. Two active proteins with properties similar to known TGF-beta 1 and TGF-beta 2 were identified. Identity was confirmed by using immunological and amino acid sequencing techniques. These results were consistent with Northern blot analysis of total BSC-1 RNA, using cDNA probes for TGF-beta 1 and TGF-beta 2, which demonstrated strong signals for both mRNAs. Metabolic labeling in conjunction with two-dimensional gel electrophoresis revealed that the cells secrete approximately 10% TGF-beta 1 and 90% TGF-beta 2.

摘要

非洲绿猴肾上皮(BSC-1)细胞条件培养基中的生长抑制活性已被证明至少部分源自转化生长因子β2(TGF-β2)[汉克斯,S.K.,阿莫尔,R.,鲍德温,J.H.,马尔多纳多,F.,斯皮斯,J.,& 霍利,R.W.(1988年)《美国国家科学院院刊》85,79 - 82],对其酸化前后的生长抑制活性进行了测试。与来自人血小板的TGF-β1类似,BSC-1细胞的抑制活性在酸化后显示出8至10倍的刺激,表明该活性以潜伏形式从细胞中分泌出来。收集BSC-1细胞的条件培养基,酸化,并通过分离TGF-β1和 -2的程序进行分级分离。通过使用BSC-细胞增殖测定法测定生物活性。鉴定出两种具有与已知TGF-β1和TGF-β2相似性质的活性蛋白。通过使用免疫和氨基酸测序技术确认了其同一性。这些结果与使用TGF-β1和TGF-β2的cDNA探针进行的BSC-1总RNA的Northern印迹分析一致,该分析显示两种mRNA均有强信号。代谢标记结合二维凝胶电泳显示,细胞分泌约10%的TGF-β1和90%的TGF-β2。

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