Feldman L, Davis K L, Feeley D M, Sytkowski A J
Laboratory for Cell and Molecular Biology, New England Deaconess Hospital, Harvard Medical School, Boston, MA 02215.
Exp Hematol. 1993 Dec;21(13):1657-62.
Erythroid colony-stimulating factor (E-CSF) is a B cell-derived membrane protein that specifically affects the growth and development of human and murine committed erythroid progenitors. We report the development of a sensitive new bioassay for E-CSF, based on the ability of the growth factor to stimulate 3H-thymidine incorporation into cloned Rauscher murine erythroleukemia cells. The assay has among its advantages the ability to measure growth factor activity on a purified target cell population in the absence of endogenous growth factor-producing accessory cells. In addition, this assay measures E-CSF's proliferative effect on erythroid progenitors in the absence of erythropoietin (Epo) after 72 to 96 hours. In contrast, the standard bone marrow fibrin clot assay traditionally used to measure E-CSF requires the addition of Epo to promote the development of hemoglobinized erythroid colonies that are quantified after 7 days (for murine cells) to 12 days (for human cells). With the use of this new Rauscher cell bioassay, we have identified an E-CSF-producing human cell line and, further, have measured E-CSF activity derived from nonhuman splenic B lymphocytes.
红细胞集落刺激因子(E-CSF)是一种B细胞衍生的膜蛋白,它特异性地影响人和小鼠定向红细胞祖细胞的生长和发育。我们报告了一种基于生长因子刺激3H-胸腺嘧啶核苷掺入克隆的劳舍尔小鼠红白血病细胞能力的新型灵敏的E-CSF生物测定法。该测定法的优点包括能够在没有内源性生长因子产生辅助细胞的情况下,在纯化的靶细胞群体上测量生长因子活性。此外,该测定法在72至96小时后,在没有促红细胞生成素(Epo)的情况下,测量E-CSF对红细胞祖细胞的增殖作用。相比之下,传统上用于测量E-CSF的标准骨髓纤维蛋白凝块测定法需要添加Epo来促进血红蛋白化红细胞集落的形成,这些集落在7天(对于小鼠细胞)至12天(对于人类细胞)后进行定量。通过使用这种新的劳舍尔细胞生物测定法,我们鉴定出了一种产生E-CSF的人类细胞系,并且进一步测量了来自非人类脾脏B淋巴细胞的E-CSF活性。