Staber F G, Burgess A W, Nicola N A, Metcalf D
Exp Hematol. 1984 Feb;12(2):107-13.
Some biological and biochemical properties of a distinct hemopoietic factor that stimulates splenic hemopoiesis in mice are described. This factor can be detected by measuring the increase in the number of in vitro hemopoietic colony-forming cells (CFCs) in the spleens of mice after transfer of serum from syngeneic donors that have been treated previously with the bacterial cell-wall components: lipid A or lipoprotein. Serum collected 5 min after the IV injection of lipid A contained almost no splenic hemopoiesis-stimulating factor (SHSF). The highest serum levels of the factor were found between 30 min and 3 h after lipid A was injected IV. The residual levels of lipid A or lipoprotein in the serum of treated mice were too low to account for their splenic hemopoiesis-stimulating effects. A component of SHSF in both post-lipid-A serum (PLAS) and postlipoprotein serum (PLPS) bound to concanavalin A (Con A)-Sepharose and could be eluted by alpha-methyglucopyranoside (0.05 M). Partial fractionation of PLAS using Con A-Sepharose and gel filtration (Sephacryl S-200) indicated that the SHSF glycoprotein had an apparent molecular weight of 30,000 daltons. SHSF was detected in serum in response to lipid A and lipoprotein, but this was separable (by gel filtration) from the major form of granulocyte-macrophage colony-stimulating factor (GM-CSF) in PLAS.
本文描述了一种能刺激小鼠脾脏造血的独特造血因子的一些生物学和生化特性。该因子可通过检测同基因供体血清转移至小鼠脾脏后,体外造血集落形成细胞(CFCs)数量的增加来检测。这些同基因供体先前已用细菌细胞壁成分:脂多糖A或脂蛋白进行处理。静脉注射脂多糖A后5分钟收集的血清几乎不含脾脏造血刺激因子(SHSF)。在静脉注射脂多糖A后30分钟至3小时之间发现该因子的血清水平最高。处理过的小鼠血清中脂多糖A或脂蛋白的残留水平过低,无法解释其对脾脏造血的刺激作用。脂多糖A后血清(PLAS)和脂蛋白后血清(PLPS)中的SHSF成分均与伴刀豆球蛋白A(Con A)-琼脂糖结合,并可用α-甲基吡喃葡萄糖苷(0.05M)洗脱。使用Con A-琼脂糖和凝胶过滤(Sephacryl S-200)对PLAS进行部分分级分离表明,SHSF糖蛋白的表观分子量为30,000道尔顿。在血清中检测到对脂多糖A和脂蛋白有反应的SHSF,但通过凝胶过滤可将其与PLAS中粒细胞-巨噬细胞集落刺激因子(GM-CSF)的主要形式分离。