Literature DB >> 9406825

Epidermal remodeling in psoriasis (II): a quantitative analysis of the epidermal architecture.

H Iizuka1, H Honda, A Ishida-Yamamoto.   

Abstract

Hyperproliferative psoriatic epidermis was quantitatively analyzed using a geometric model of viable epidermis. Our model was based on hexagonally arranged cylindrical papillae, which allowed the determination of the total volume of the viable epidermis and the total area of the interface with the proliferative compartment based on several parameters, such as papillary height, papillary width, and distance between neighboring papillae. The analysis assumed that the total number of viable epidermal cells paralleled the proliferative compartment in a steady state of cell flow, so a quantitative relation could be made between both volume and interface of the viable epidermis. Multiple parameters of the psoriatic epidermal architecture were measured, and variations within psoriasis were predicted by the model. The results predicted were remarkably close to the observed values. The geometric model also indicated that psoriatic epidermis could be subdivided into two distinct types, with and without a granular layer; the latter having a shorter turnover time. This is consistent with the notion that the typical psoriatic epidermis (without the granular layer) represents the expanding hyperproliferative phase, whereas the psoriatic epidermis with a granular layer represents stationary or resolving states. The model of hexagonally arranged cylindrical papillae suggested that the architecture of the psoriatic epidermis is constructed by a simple mechanism, whereby the psoriatic angulated rete-papilla pattern was produced by a two-dimensional increase in the proliferative compartment and a three-dimensional increase in the total volume of the viable epidermis.

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Year:  1997        PMID: 9406825     DOI: 10.1111/1523-1747.ep12341002

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  3 in total

1.  Epidermal kinetic alterations required to generate the psoriatic phenotype: a reappraisal.

Authors:  T Simonart; M Heenen; O Lejeune
Journal:  Cell Prolif       Date:  2010-06       Impact factor: 6.831

2.  Interferon-gamma-dependent stimulation of human involucrin gene expression: STAT1 (signal transduction and activators of transcription 1) protein activates involucrin promoter activity.

Authors:  H Takahashi; K Asano; S Nakamura; A Ishida-Yamamoto; H Iizuka
Journal:  Biochem J       Date:  1999-12-15       Impact factor: 3.857

3.  CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-alpha OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO.

Authors:  Hidetoshi Takahashi; Hitomi Tsuji; Yoshio Hashimoto; Akemi Ishida-Yamamoto; Hajime Iizuka
Journal:  Indian J Dermatol       Date:  2009-07       Impact factor: 1.494

  3 in total

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