Stoppacciaro A, Bossu P, Ghiara P, Ruco L P, Censini S, Scapigliati G, Nuti S, Tagliabue A, Baroni C D, Boraschi D
Department of Human Biopathology, University La Sapienza, Roma, Italy.
J Immunol. 1991 Sep 1;147(5):1561-6.
To gain information on the possible biologic role of IL-1R type II (IL-1RII), expression of the 68-kDa IL-1 binding protein on human lymphoblastoid B cells was investigated at single cell level. Binding of iodinated IL-1 beta was evaluated by autoradiography on cytosmears of IL-1RII positive B cell lines RAJI, the RAJI clone 1H7, and STS 25. Results obtained suggest an heterogeneity of IL-1RII expression within the B cell population, with only 5 to 16% of the cells able to bind IL-1 beta. Up-regulation of IL-1RII expression by dexamethasone, evident in conventional binding assays, was achieved through both increase in the number of IL-1 binding cells (14-30%) and augmentation of receptor density on positive cells, By combining autoradiography with immunocytochemical staining, it could be shown that about 80% of IL-1RII + cells were negative for Ki67, a nuclear antigen expressed from late G1 to M phase. Cell cycle dependent expression of IL-1RII was confirmed on cells enriched in different phases of the cell cycle by counterflow centrifugal elutriation. It is thus proposed that IL-1RII is associated to the cell cycle.
为了获取有关Ⅱ型白细胞介素-1受体(IL-1RII)可能的生物学作用的信息,在单细胞水平上研究了人淋巴母细胞样B细胞上68 kDa白细胞介素-1结合蛋白的表达。通过放射自显影法对IL-1RII阳性B细胞系RAJI、RAJI克隆1H7和STS 25的细胞涂片进行碘化白细胞介素-1β结合评估。所得结果提示B细胞群体中IL-1RII表达存在异质性,只有5%至16%的细胞能够结合白细胞介素-1β。地塞米松对IL-1RII表达的上调在传统结合试验中很明显,这是通过增加IL-1结合细胞的数量(14% - 30%)以及阳性细胞上受体密度的增加实现的。通过将放射自显影与免疫细胞化学染色相结合,可以发现约80%的IL-1RII +细胞Ki67呈阴性,Ki67是一种从G1期晚期到M期表达的核抗原。通过逆流离心淘析对富集于细胞周期不同阶段的细胞进行研究,证实了IL-1RII的细胞周期依赖性表达。因此,有人提出IL-1RII与细胞周期相关。