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血影蛋白在体内和体外角质形成细胞中的分布。

Distribution of fodrin in the keratinocyte in vivo and in vitro.

作者信息

Yoneda K, Fujimoto T, Imamura S, Ogawa K

机构信息

Department of Dermatology, Faculty of Medicine, Kyoto University, Japan.

出版信息

J Invest Dermatol. 1990 May;94(5):724-9. doi: 10.1111/1523-1747.ep12876298.

Abstract

Distribution of fodrin in the keratinocyte, both in vivo and in vitro, was examined by immunofluorescence microscopy. In the rat epidermis in vivo, fodrin was localized in the cell periphery of the spinous layer of all the skins studied. In only the basal layer of the thick skin, however, fodrin was seen intensely in the cytoplasm. As in vitro keratinocytes, a mouse cell line (Pam 212) cultured in low (0.06 mM) as well as standard (1.87 mM) Ca2+ was examined. In low Ca2+, fodrin was observed throughout the cytoplasm without marked accumulation irrespective of the cell density. The cytoplasmic labeling in low Ca2+ looked filamentous and became aggregated when cells were treated with cytochalasin B; at least some of the aggregates coexisted with those of F-actin. In contrast, fodrin distribution was not affected with colchicine. On the other hand, in standard Ca2+, the protein became concentrated along the cell periphery and less conspicuous in the cytoplasm as the cells reached confluency. When cells were transferred from low to standard Ca2+, the distribution of fodrin changed accordingly within 180 min. The present results indicate that fodrin in the keratinocyte is likely to be associated with actin filaments and that it takes two different ways of distribution both in vivo and in vitro. The peripheral and the cytoplasmic labeling of in vivo and in vitro cells are likely to correspond. It may be that fodrin changes its localization according to the cell's proliferative activity.

摘要

通过免疫荧光显微镜检查了 fodrin 在体内和体外角质形成细胞中的分布。在体内大鼠表皮中,fodrin 定位于所有研究皮肤棘层的细胞周边。然而,仅在厚皮的基底层中,fodrin 在细胞质中强烈可见。对于体外角质形成细胞,研究了在低钙(0.06 mM)以及标准钙(1.87 mM)中培养的小鼠细胞系(Pam 212)。在低钙条件下,无论细胞密度如何,fodrin 在整个细胞质中均有观察到,无明显聚集。低钙条件下的细胞质标记看起来呈丝状,在用细胞松弛素 B 处理细胞时会聚集;至少一些聚集体与 F-肌动蛋白的聚集体共存。相比之下,秋水仙碱不影响 fodrin 的分布。另一方面,在标准钙条件下,随着细胞达到汇合状态,该蛋白沿细胞周边浓缩,在细胞质中不那么明显。当细胞从低钙转移到标准钙时,fodrin 的分布在 180 分钟内相应改变。目前的结果表明,角质形成细胞中的 fodrin 可能与肌动蛋白丝相关,并且在体内和体外都有两种不同的分布方式。体内和体外细胞的周边和细胞质标记可能相对应。可能是 fodrin 根据细胞的增殖活性改变其定位。

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