Sandilands G P, Burnett E R, MacPherson S A, Downie I, More I A, MacSween R N
University Department of Pathology, Western Infirmary, Glasgow, UK.
Immunology. 1997 Mar;90(3):427-34. doi: 10.1111/j.1365-2567.1997.00427.x.
We have recently described a cytoplasmic from of CD32 (Fc gamma RII) within the vast majority of normal human peripheral blood lymphocytes (PBL) including T cells. The function of cytoplasmic CD32 is not known. These flow cytometric studies were conducted using single cell suspensions of PBL that had been pre-fixed and permeabilized using methanol/triton-X-100. In this study we have attempted to visualize cytoplasmic CD32 by immunocytochemistry using normal PBL processed in various ways and have also looked for CD32 within tissue lymphocytes. Weak cytoplasmic CD32 staining was observed in paraffin sections of normal lymphocytes but only when sections were microwave treated. The intensity of staining for CD32 did however, appear to be much stronger within infiltrating lymphocytes found in autoimmune diseases or in rejecting allografts: an observation that suggests that up-regulation of cytoplasmic CD32 may occur when T cells become activated in vivo. Microwave treatment of PBL suspensions was shown to disrupt the outer cell membrane, thus effectively permeabilizing the cell and allowing for the detection of cytoplasmic components, like CD32, by flow cytometry. Microwave treatment may, therefore, afford an alternative method for cell permeabilization and may prove to be a useful method for the study of cytoplasmic molecules in cell suspensions and in paraffin-embedded tissues.
我们最近描述了在绝大多数正常人外周血淋巴细胞(PBL)包括T细胞内存在一种胞质形式的CD32(FcγRII)。胞质CD32的功能尚不清楚。这些流式细胞术研究使用的是经甲醇/曲拉通-X-100预固定和通透处理的PBL单细胞悬液。在本研究中,我们尝试通过免疫细胞化学方法,利用以各种方式处理的正常PBL来观察胞质CD32,并且还在组织淋巴细胞中寻找CD32。在正常淋巴细胞的石蜡切片中观察到了微弱的胞质CD32染色,但仅在切片经微波处理时才出现。然而,在自身免疫性疾病或移植排斥反应中浸润的淋巴细胞内,CD32的染色强度似乎要强得多:这一观察结果表明,当T细胞在体内被激活时,胞质CD32可能会上调。结果显示,对PBL悬液进行微波处理会破坏细胞膜外层,从而有效地使细胞通透,使得通过流式细胞术能够检测到胞质成分,如CD32。因此,微波处理可能提供一种细胞通透的替代方法,并且可能被证明是研究细胞悬液和石蜡包埋组织中胞质分子的一种有用方法。