Kubo M, Ohno S, Kato M, Isemura M, Tagami H, Saida T
Department of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan.
Arch Dermatol Res. 1994;286(8):448-54. doi: 10.1007/BF00371570.
We investigated the ultrastructural localization of fibronectin (FN) in cultured human keratinocytes using an improved method of peroxidase-immunoelectron microscopy. This method enabled us to visualize the precise localization of FN within the cells while preserving the morphology. FN was localized in the protein synthetic and secretory organelles, including the rough-surfaced endoplasmic reticulum, Golgi complex, multivesicular bodies and perinuclear space. It was also detected in the extracellular space, on small regions of the villous projections of cell membranes at the site of secretion and at cell-substratum contact sites. These findings confirm that human keratinocytes synthesize, secrete and deposit FN in the pericellular matrix.
我们使用一种改进的过氧化物酶免疫电子显微镜方法,研究了纤连蛋白(FN)在培养的人角质形成细胞中的超微结构定位。这种方法使我们能够在保持细胞形态的同时,观察到FN在细胞内的精确定位。FN定位于蛋白质合成和分泌细胞器,包括糙面内质网、高尔基体、多囊泡体和核周间隙。在细胞外空间、分泌部位细胞膜绒毛状突起的小区域以及细胞与基质接触部位也检测到了FN。这些发现证实人角质形成细胞在细胞周围基质中合成、分泌并沉积FN。