Waheed A, Shadduck R K
Department of Medicine, Montefiore Hospital, University of Pittsburgh School of Medicine, Pennsylvania 15213.
Proc Soc Exp Biol Med. 1988 Jan;187(1):69-75. doi: 10.3181/00379727-187-42639.
125I-labeled colony-stimulating factor (CSF) binds to granulocytic and monocytic cells in the bone marrow in an irreversible manner. Addition of a 1000-fold excess of unlabeled CSF does not displace the bound material. The present studies showed that brief exposures to pH 2.7-5.0 caused a marked release of the bound material. Such treatments were nontoxic to the marrow cells as judged by trypan blue dye exclusion, assay of colony-forming cells, and by analysis of rebinding of fresh 125I-CSF to the acid-treated cells. The CSF released from marrow cells by low pH revealed two peaks of radioactivity on SDS-acrylamide gel. The first peak (67,500 Da) corresponded to native CSF; a second peak of 53,500 Da was observed. Despite this apparent mild degradation of CSF, the released material showed greater binding to marrow and greater precipitation by anti-CSF than the native 125I-CSF. Further studies showed that acid treatment of marrow cells led to stabilization of the CSF receptors. Pretreatment at pH 4.0 led to retention of binding sites after conversion of marrow cultures to pH 7.5 and incubation at 22-37 degrees C. In contrast, cells that were not exposed to low pH lost receptors rapidly at these temperatures. The extent of preservation of the binding sites was related to the duration of acid exposure. These studies indicate that CSF is retained on the cell surface after binding at 0 degree C and that the CSF can be eluted by acid conditions.(ABSTRACT TRUNCATED AT 250 WORDS)
125I标记的集落刺激因子(CSF)以不可逆的方式与骨髓中的粒细胞和单核细胞结合。加入1000倍过量的未标记CSF并不能取代已结合的物质。目前的研究表明,短暂暴露于pH 2.7 - 5.0会导致已结合物质的显著释放。通过台盼蓝染料排斥试验、集落形成细胞测定以及新鲜125I - CSF与酸处理细胞再结合的分析判断,此类处理对骨髓细胞无毒。低pH从骨髓细胞中释放的CSF在SDS - 聚丙烯酰胺凝胶上显示出两个放射性峰。第一个峰(67,500道尔顿)对应天然CSF;观察到第二个峰为53,500道尔顿。尽管CSF明显有轻度降解,但释放的物质比天然125I - CSF显示出与骨髓更强的结合以及更强的抗CSF沉淀。进一步研究表明,骨髓细胞的酸处理导致CSF受体稳定。在pH 4.0预处理导致骨髓培养物转换至pH 7.5并在22 - 37摄氏度孵育后结合位点得以保留。相反,未暴露于低pH的细胞在这些温度下迅速失去受体。结合位点的保留程度与酸暴露的持续时间有关。这些研究表明,CSF在0摄氏度结合后保留在细胞表面,并且CSF可通过酸性条件洗脱。(摘要截短于250字)