Login G R, Galli S J, Morgan E, Arizono N, Schwartz L B, Dvorak A M
Department of Pathology, Harvard School of Dental Medicine, Beth Israel Hospital, Boston, Massachusetts.
Lab Invest. 1987 Nov;57(5):592-9.
We defined the ultrastructural localization of chymase in rat peritoneal mast cells using standard aldehyde fixation and a newly described microwave fixation method (Login GR, Dvorak AM: Microwave energy fixation for electron microscopy. Am J Pathol 120: 230, 1985; Login GR, Stavinoha WB, Dvorak AM: Ultrafast microwave energy fixation for electron microscopy. J Histochem Cytochem 34:381, 1986) and postembedding immunogold labeling. Thin sections were exposed first to goat IgG anti-rat chymase and second to gold-conjugated rabbit Ig directed against goat IgG. By transmission electron microscopy, gold particles were localized to the matrix of cytoplasmic granules. Control sections treated with nonimmune sera did not exhibit labeling of mast cells. Thin sections treated simultaneously with purified rat mast cell chymase and anti-chymase antibody in competition studies, showed a marked reduction in granule staining. These findings demonstrate that a microwave fixation method can be used to rapidly fix cell suspensions for postembedding immunocytochemical studies.
我们使用标准醛固定法和一种新描述的微波固定法(Login GR,Dvorak AM:用于电子显微镜的微波能量固定。《美国病理学杂志》120:230,1985;Login GR,Stavinoha WB,Dvorak AM:用于电子显微镜的超快微波能量固定。《组织化学与细胞化学杂志》34:381,1986)以及包埋后免疫金标记法,确定了大鼠腹膜肥大细胞中糜酶的超微结构定位。超薄切片首先与山羊抗大鼠糜酶IgG接触,然后与针对山羊IgG的金标记兔Ig接触。通过透射电子显微镜观察,金颗粒定位于细胞质颗粒的基质中。用非免疫血清处理的对照切片未显示肥大细胞有标记。在竞争研究中,同时用纯化的大鼠肥大细胞糜酶和抗糜酶抗体处理的超薄切片,颗粒染色明显减少。这些发现表明,微波固定法可用于快速固定细胞悬液,以进行包埋后免疫细胞化学研究。