Barabasi K, Nässberger L
Department of Clinical Immunology and Medical Microbiology, Lund University, Sweden.
APMIS. 1994 Feb;102(2):89-93. doi: 10.1111/j.1699-0463.1994.tb04851.x.
We have investigated the distribution of cathepsin D in mononuclear and polymorphonuclear cells using an anti-rabbit human cathepsin D antibody and indirect immunofluorescence. Lymphocytes showed the same fluorescence intensity as control cells incubated with normal serum. Fluorescence staining patterns of polymorphonuclear cells differed according to the fixative used. Monocytes and granulocytes fixed in ethanol, methanol, glutaraldehyde, and Bouin's fixative caused a homogeneous cytoplasmic staining with a distinct nuclear sparing. A perinuclear staining was seen in acetone-fixed cells in both monocytes and granulocytes. Another interesting difference was observed between monocytes and granulocytes when formalin was used as fixative. Monocytes appeared with a cytoplasmic staining, but in formalin-fixed granulocytes redistribution to the nuclear membrane was seen.
我们使用抗兔人组织蛋白酶D抗体和间接免疫荧光法研究了组织蛋白酶D在单核细胞和多形核细胞中的分布。淋巴细胞显示出与用正常血清孵育的对照细胞相同的荧光强度。多形核细胞的荧光染色模式因所用固定剂而异。用乙醇、甲醇、戊二醛和波因氏固定剂固定的单核细胞和粒细胞导致均匀的细胞质染色,细胞核明显不着色。在丙酮固定的单核细胞和粒细胞中均可见核周染色。当使用福尔马林作为固定剂时,在单核细胞和粒细胞之间观察到另一个有趣的差异。单核细胞出现细胞质染色,但在福尔马林固定的粒细胞中可见重新分布至核膜。