Literature DB >> 7531997

Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis).

A Ishida-Yamamoto1, R A Eady, R A Underwood, B A Dale, K A Holbrook.   

Abstract

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.

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Year:  1994        PMID: 7531997     DOI: 10.1111/j.1365-2133.1994.tb08578.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  5 in total

1.  Formation of a normal epidermis supported by increased stability of keratins 5 and 14 in keratin 10 null mice.

Authors:  J Reichelt; H Büssow; C Grund; T M Magin
Journal:  Mol Biol Cell       Date:  2001-06       Impact factor: 4.138

2.  Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature.

Authors:  Kunal Malik; Helen He; Thy Nhat Huynh; Gary Tran; Kelly Mueller; Kristina Doytcheva; Yael Renert-Yuval; Tali Czarnowicki; Shai Magidi; Margaret Chou; Yeriel D Estrada; Huei-Chi Wen; Xiangyu Peng; Hui Xu; Xiuzhong Zheng; James G Krueger; Amy S Paller; Emma Guttman-Yassky
Journal:  J Allergy Clin Immunol       Date:  2018-05-24       Impact factor: 10.793

3.  Impaired hair follicle morphogenesis and cycling with abnormal epidermal differentiation in nackt mice, a cathepsin L-deficient mutation.

Authors:  Fernando Benavides; Matthew F Starost; Mónica Flores; Irma B Gimenez-Conti; Jean-Louis Guénet; Claudio J Conti
Journal:  Am J Pathol       Date:  2002-08       Impact factor: 4.307

4.  Altered distribution of keratinization markers in epidermolytic hyperkeratosis.

Authors:  A Ishida-Yamamoto; H Iizuka; M Manabe; W M O'Guin; D Hohl; T Kartasova; T Kuroki; D R Roop; R A Eady
Journal:  Arch Dermatol Res       Date:  1995       Impact factor: 3.017

Review 5.  Cracking the Skin Barrier: Liquid-Liquid Phase Separation Shines under the Skin.

Authors:  Alexa Regina Chua Avecilla; Felipe Garcia Quiroz
Journal:  JID Innov       Date:  2021-07-06
  5 in total

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