Ishida-Yamamoto A, Eady R A, Underwood R A, Dale B A, Holbrook K A
St John's Institute of Dermatology, St Thomas' Hospital, London, U.K.
Br J Dermatol. 1994 Dec;131(6):767-79. doi: 10.1111/j.1365-2133.1994.tb08578.x.
To evaluate the role of filaggrin in keratin filament aggregation in epidermolytic ichthyosis (epidermolytic hyperkeratosis, EH), we studied EH skin by light and electron microscopic immunohistochemistry, and biochemical analysis using sodium dodecylsulphate-polyacrylamide gel electrophoresis and immunoblotting. Immunohistochemical staining showed an increased number of filaggrin-immunoreactive cell layers, but the reaction was still confined to the mid- and upper epidermal layers, whereas an abnormal granular pattern of staining for K10 began in the lower suprabasal cell layers. This suggests that the aggregation of keratin filaments precedes, and occurs independently of, profilaggrin synthesis during epidermal differentiation. Although keratohyalin granules were frequently associated with clumped filaments, immunoelectron microscopy showed that K10 labelling was confined to keratin filaments (including clumped filaments), and that antifilaggrin antibodies stained only keratohyalin granules, at least in the living cells. Certain keratin aggregates in the cornified cells were still devoid of filaggrin staining. However, in some cells which appeared partially cornified, filaggrin immunoreactivity occurred over the aggregated keratin filaments. Immunoblotting showed a clear increase of filaggrin/profilaggrin expression, without evidence for a qualitative abnormality. It seems unlikely, therefore, that filaggrin is primarily involved in the keratin filament clumping in EH, but that in some EH cases it interacts with keratins in a defective manner, possibly due to premature cell death and profilaggrin processing and/or altered keratin filament structure involving the interaction points of keratin with filaggrin.
为了评估聚角蛋白微丝蛋白在表皮松解性鱼鳞病(表皮松解性角化过度症,EH)中角蛋白丝聚集过程中的作用,我们通过光镜和电镜免疫组织化学以及使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和免疫印迹的生化分析方法对EH皮肤进行了研究。免疫组织化学染色显示聚角蛋白微丝蛋白免疫反应阳性的细胞层数增加,但反应仍局限于表皮中层和上层,而K10的异常颗粒状染色则始于基底上层细胞层的下部。这表明在表皮分化过程中,角蛋白丝的聚集先于聚角蛋白前体的合成,并且独立于其发生。尽管透明角质颗粒经常与聚集的细丝相关,但免疫电子显微镜显示K10标记仅限于角蛋白丝(包括聚集的细丝),并且抗聚角蛋白微丝蛋白抗体至少在活细胞中仅染色透明角质颗粒。角质化细胞中的某些角蛋白聚集体仍然没有聚角蛋白微丝蛋白染色。然而,在一些部分角质化的细胞中,聚角蛋白微丝蛋白免疫反应性出现在聚集的角蛋白丝上。免疫印迹显示聚角蛋白微丝蛋白/聚角蛋白前体的表达明显增加,没有定性异常的证据。因此,聚角蛋白微丝蛋白似乎不太可能主要参与EH中的角蛋白丝聚集,但在某些EH病例中,它可能以缺陷的方式与角蛋白相互作用,这可能是由于细胞过早死亡、聚角蛋白前体加工和/或涉及角蛋白与聚角蛋白微丝蛋白相互作用点的角蛋白丝结构改变所致。