Chikanza I C, Corrigal V, Kingsley G, Panayi G S
Rheumatology Unit, UMDS of Guy's Hospital, London, UK.
J Immunol Methods. 1992 Oct 2;154(2):173-8. doi: 10.1016/0022-1759(92)90189-z.
A technique for intracytoplasmic immunofluorescence staining to detect and quantify human interleukin-1 alpha (IL-1 alpha) and beta (IL-1 beta) in CD4, CD8, and CD14 positive lymphoid cells is described. Mononuclear cells stimulated in vitro with PHA to produce IL-1, were fixed and made permeable to antibodies by sequential exposure to paraformaldehyde and the detergent n-octyl-glucoside. Cytoplasmic and surface staining of both forms of IL-1 were demonstrated by indirect fluorescence using IL-1 beta and IL-1 alpha specific mouse monoclonal antibodies and quantified with flow cytometry.
本文描述了一种用于胞质免疫荧光染色的技术,该技术可检测和定量CD4、CD8和CD14阳性淋巴细胞中的人白细胞介素-1α(IL-1α)和β(IL-1β)。用PHA体外刺激产生IL-1的单核细胞,通过依次暴露于多聚甲醛和去污剂正辛基葡萄糖苷进行固定并使抗体可通透进入细胞。使用IL-1β和IL-1α特异性小鼠单克隆抗体通过间接荧光法对两种形式的IL-1进行细胞质和表面染色,并通过流式细胞术进行定量分析。