Simulating psoriasis by altering transit amplifying cells.

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Simulating psoriasis by altering transit amplifying cells. / Grabe, Niels; Neuber, Karsten.

In: BIOINFORMATICS, Vol. 23, No. 11, 11, 2007, p. 1309-1312.

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Grabe N, Neuber K. Simulating psoriasis by altering transit amplifying cells. BIOINFORMATICS. 2007;23(11):1309-1312. 11.

Bibtex

@article{d284f343a06b457481352a956a5a3a97,
title = "Simulating psoriasis by altering transit amplifying cells.",
abstract = "Computational models of tissue homeostasis will facilitate a deeper understanding of many diseases. They link molecular networks, cellular differentiation and the spatial and temporal organization of tissues. Here we show an approach which is able to computationally turn a healthy in silico epidermis into one with four central properties of psoriatic epidermis. We achieve this by altering a single simulation parameter in the cellular differentiation program of the simulated epidermal keratinocytes: the fractional time period during which transit amplifying cells proliferate (tau). Prolonging tau results in the four main pathological characteristics of psoriatic skin: (1) an absolute increase of the germinative compartment, (2) an absolute increase of the differentiated compartment, (3) a higher proportion of germinative cells and (4) a marked reduction in turnover time. The prolongation of tau is able to increase the proliferation capacity of the epidermal tissue without altering the cell cycle frequency.",
author = "Niels Grabe and Karsten Neuber",
year = "2007",
language = "Deutsch",
volume = "23",
pages = "1309--1312",
journal = "BIOINFORMATICS",
issn = "1367-4803",
publisher = "Oxford University Press",
number = "11",

}

RIS

TY - JOUR

T1 - Simulating psoriasis by altering transit amplifying cells.

AU - Grabe, Niels

AU - Neuber, Karsten

PY - 2007

Y1 - 2007

N2 - Computational models of tissue homeostasis will facilitate a deeper understanding of many diseases. They link molecular networks, cellular differentiation and the spatial and temporal organization of tissues. Here we show an approach which is able to computationally turn a healthy in silico epidermis into one with four central properties of psoriatic epidermis. We achieve this by altering a single simulation parameter in the cellular differentiation program of the simulated epidermal keratinocytes: the fractional time period during which transit amplifying cells proliferate (tau). Prolonging tau results in the four main pathological characteristics of psoriatic skin: (1) an absolute increase of the germinative compartment, (2) an absolute increase of the differentiated compartment, (3) a higher proportion of germinative cells and (4) a marked reduction in turnover time. The prolongation of tau is able to increase the proliferation capacity of the epidermal tissue without altering the cell cycle frequency.

AB - Computational models of tissue homeostasis will facilitate a deeper understanding of many diseases. They link molecular networks, cellular differentiation and the spatial and temporal organization of tissues. Here we show an approach which is able to computationally turn a healthy in silico epidermis into one with four central properties of psoriatic epidermis. We achieve this by altering a single simulation parameter in the cellular differentiation program of the simulated epidermal keratinocytes: the fractional time period during which transit amplifying cells proliferate (tau). Prolonging tau results in the four main pathological characteristics of psoriatic skin: (1) an absolute increase of the germinative compartment, (2) an absolute increase of the differentiated compartment, (3) a higher proportion of germinative cells and (4) a marked reduction in turnover time. The prolongation of tau is able to increase the proliferation capacity of the epidermal tissue without altering the cell cycle frequency.

M3 - SCORING: Zeitschriftenaufsatz

VL - 23

SP - 1309

EP - 1312

JO - BIOINFORMATICS

JF - BIOINFORMATICS

SN - 1367-4803

IS - 11

M1 - 11

ER -