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银屑病病理生理学的细胞动力学基础。

Cell kinetic basis for pathophysiology of psoriasis.

作者信息

Weinstein G D, McCullough J L, Ross P A

出版信息

J Invest Dermatol. 1985 Dec;85(6):579-83. doi: 10.1111/1523-1747.ep12283594.

DOI:10.1111/1523-1747.ep12283594
PMID:4067329
Abstract

Studies on the cell proliferation kinetics of psoriatic epidermal cells are presented and the results compared to similar studies for normal epidermis. The short 36-h duration of the psoriatic cell cycle (Tc) is confirmed with the first double-peaked fraction of labeled mitoses (FLM) curve in human subjects. The growth fraction of psoriasis using two experimental techniques approximates 100% within 36 h, confirming the rapid Tc found by the FLM method. The cell kinetic basis for the pathophysiology of psoriasis consists of at least 3 proliferative abnormalities in comparison to normal epidermis. By far the largest alteration is the shortening of the Tc from 311 to 36 h. There is also a doubling of the proliferative cell population in psoriasis from 27,000 to 52,000 cells/mm and an increase in the growth fraction from 60% to 100%. As a consequence of these abnormalities the psoriatic epidermis produces 35,000 cells/day from a proliferative compartment of 52,000 cells/mm2 surface area. This is a 28-fold greater production of cells than the 1,246 cells/day produced in normal epidermis. The biochemical or control factors leading to these kinetic differences continue to remain elusive.

摘要

本文介绍了银屑病表皮细胞的细胞增殖动力学研究,并将结果与正常表皮的类似研究进行了比较。在人类受试者中,通过标记有丝分裂的第一个双峰部分(FLM)曲线,证实了银屑病细胞周期(Tc)较短,为36小时。使用两种实验技术,银屑病的生长分数在36小时内接近100%,证实了通过FLM方法发现的快速Tc。与正常表皮相比,银屑病病理生理学的细胞动力学基础至少包括3种增殖异常。到目前为止,最大的变化是Tc从311小时缩短到36小时。银屑病中增殖细胞群体也增加了一倍,从27,000个细胞/mm增加到52,000个细胞/mm,生长分数从60%增加到100%。由于这些异常,银屑病表皮从每平方毫米表面积52,000个细胞的增殖区每天产生35,000个细胞。这是正常表皮每天产生1,246个细胞的28倍。导致这些动力学差异的生化或控制因素仍然难以捉摸。

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1
Cell kinetic basis for pathophysiology of psoriasis.银屑病病理生理学的细胞动力学基础。
J Invest Dermatol. 1985 Dec;85(6):579-83. doi: 10.1111/1523-1747.ep12283594.
2
Cell proliferation in normal epidermis.正常表皮中的细胞增殖。
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The cell cycle in psoriasis: a reappraisal.银屑病中的细胞周期:重新评估。
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Altered [125I]epidermal growth factor binding and receptor distribution in psoriasis.银屑病中[125I]表皮生长因子结合及受体分布的改变
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