Pinkston J A, Finch S C
Stain Technol. 1979 Sep;54(5):233-9. doi: 10.3109/10520297909110677.
This report describes alterations in the agarose lymphocyte migration technique which resulted in satisfactory differentiation of T and B lymphocytes and monocytes which have migrated as a monolayer for 1-3 days. The Wright-Giemsa staining used in the original method did not permit identification of individual migrating cell types. The most important modifications were changing from a plastic to a glass migration surface, and significantly reducing the overlying thickness of agarose which permitted a short fixation time and easy preparation of permanent slides stained for nonspecific esterase. The esterase staining of monocyte cytoplasm was intense and diffuse. One or two small, discrete areas of cytoplasmic esterase activity were identified in the majority of T lymphocytes. B lymphocytes showed either a trace or no evidence of esterase activity. The modified method should prove useful for the histochemical differentiation of migrating subpopulations of mononuclear cells.
本报告描述了琼脂糖淋巴细胞迁移技术的改进,该技术能使迁移1至3天形成单层的T淋巴细胞、B淋巴细胞和单核细胞得到令人满意的区分。原方法中使用的瑞氏-吉姆萨染色无法识别单个迁移细胞类型。最重要的改进是将迁移表面从塑料改为玻璃,并显著减小琼脂糖覆盖厚度,这使得固定时间缩短,且便于制备用于非特异性酯酶染色的永久玻片。单核细胞胞质的酯酶染色强烈且弥漫。在大多数T淋巴细胞中可识别出一两个小的、离散的胞质酯酶活性区域。B淋巴细胞显示出微量酯酶活性或无酯酶活性迹象。改进后的方法应证明对单核细胞迁移亚群的组织化学区分有用。