Honigwachs-Sha'anani J, Brosh N, Kompier R, Kadouri A, Zipori D
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Ann N Y Acad Sci. 1991;628:287-97. doi: 10.1111/j.1749-6632.1991.tb17259.x.
MBA-2.1 cells produce an activity, designated restrictin-P, which is specifically inhibitory to the growth of plasmacytomas and mature B cell lymphomas. We examined whether the activity of this stromally derived glycoprotein could be attributed to a well-characterized growth factor. Restrictin-P-producing cells were therefore screened for the expression of transcripts of a variety of growth suppressors. With the exception of TGF-beta 1, none was produced in detectable amounts by these cells. Furthermore, recombinant forms of the inhibitory molecules tested did not exert a biological effect similar to that of restrictin-P. Restrictin-P was shown to elicit a G0/G1 arrest in the cell cycle of its target cells, as soon as 24 h after their exposure to the inhibitor. This effect could not be mimicked by TGF-beta 1. We suggest that restrictin-P is part of a novel family of inhibitors which are required for the maintenance of cell-type specificities in the hematopoietic microenvironment.
MBA - 2.1细胞产生一种名为限制素 - P的活性物质,它对浆细胞瘤和成熟B细胞淋巴瘤的生长具有特异性抑制作用。我们研究了这种基质衍生糖蛋白的活性是否可归因于一种特征明确的生长因子。因此,对产生限制素 - P的细胞进行了多种生长抑制因子转录本表达的筛选。除了转化生长因子 - β1外,这些细胞未检测到产生其他可检测量的因子。此外,所测试的抑制分子的重组形式并未发挥与限制素 - P类似的生物学效应。限制素 - P被证明在其靶细胞接触抑制剂后24小时内,就能使其细胞周期停滞在G0/G1期。转化生长因子 - β1无法模拟这种效应。我们认为限制素 - P是一类新型抑制剂家族的成员,这些抑制剂是维持造血微环境中细胞类型特异性所必需的。