Ultrastructural localization of desmoglein and plakophilin in the human hair suggests that the cell membrane complex is a long desmosomal remnant

被引:3
作者
Alibardi, Lorenzo [1 ,2 ]
Tsuchiya, Masaru [3 ]
Watanabe, Shunichi [3 ]
Noecker, Bernd [4 ]
机构
[1] Univ Bologna, Comparat Histolab, I-40126 Bologna, Italy
[2] Univ Bologna, Dipt Biol, I-40126 Bologna, Italy
[3] Kao Corp, Hair Beauty Lab, Global R&D, Tokyo 1318501, Japan
[4] Kao Germany GmbH, Kao European Res Lab, D-64297 Darmstadt, Germany
关键词
Human hair; Keratinizing zone; Desmosomal proteins; Immunogold; Ultrastructure; KERATINIZING CELLS; WOOL FOLLICLE; COMPANION LAYER; DIFFERENTIATIONS; PROTEINS; CORTEX;
D O I
10.1016/j.acthis.2013.04.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Unlike the superficial part of the corneous layer of the epidermis (Stratum corneum) where desmosomes are degraded and corneocytes flake away, the trichocytes in the hair remain attached to each other after cornification. The permanence and fine localization of cell junctions, in particular of desmosomal proteins in the cornifying and mature human hair, is not known. The present electron microscope immunolocalization study indicates that two protein markers for desmosomes such as desmoglein 4 and plakophilins 1 and 3 are still present in mature cortical and cuticle cells. These proteins remain mainly localized in the cornified cytoplasmic side of desmosomal remnants of cortical cells, but also in the delta layer of the extracellular region of the membrane complex. This suggests that the delta layer represents an extensive desmosomal remnant formed between mature cortical cells and in cuticle cells. The endocuticle appears to be the site of accumulation of desmosomal proteins and degraded nuclear material. The cornification of desmosomal junctions in both cortical and cuticle cells likely contributes to stabilize the integrity of the hair shaft. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:879 / 886
页数:8
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