The role of adhesion molecules, chemotactic factors, and cytokines in inflammatory and neoplastic skin disease--1990 update.
The role of adhesion molecules, chemotactic factors, and cytokines in inflammatory and neoplastic skin disease--1990 update.
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粘附分子、趋化因子和细胞因子在炎症和肿瘤性皮肤病中的作用 - 1990 年更新。
DOI:
10.1111/1523-1747.ep12876134
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发表时间:
1990
期刊:
影响因子:
--
通讯作者:
Barker,JN
中科院分区:
文献类型:
--
作者:
Nickoloff,BJ;Griffiths,CE;Barker,JN
In 1986 it was discovered that cultured human keratinocytes, when treated with gamma interferon, attract and bind T lymphocytes and monocytes. More is now known about trafficking of inflammatory cells in the skin, with specific molecular details involving various cytokines, chemotactic factors, and adhesion molecules. One key element is the in vivo movement of T cells that express LFA-1 into the epidermis, and their subsequent binding to keratinocytes via the surface expression of intercellular adhesion molecule-1 (ICAM-1). This interaction represents a common immunologic pathway, which has been identified in a wide variety of different skin diseases. This review provides a synopsis of advances in this field, which have grown rapidly during the past few years, and adds recent results dealing with coordinate regulation at the gene-transcriptional level of keratinocyte chemotactic factor production and adhesion molecule expression. Moreover, epidermal keratinocytes appear to play a pre-eminent role in the skin, serving as transducing elements converting exogenously applied low-molecular-weight chemical stimuli such as phorbol ester and urushiol (the active ingredient in poison ivy extracts) into the production of endogenously derived immunoregulatory proteins. These keratinocyte-derived molecules may then influence immunocytes and endothelial cells to further amplify the inflammatory response. The identification of keratinocyte-derived molecules such as IL-8 and ICAM-1, which influence the chemotaxis and adherence of T cells, adds substantial evidence supporting an active participatory role for keratinocytes in cutaneous immunohomeostasis. Finally, we highlight the importance of these immunoregulatory molecules in two malignant cutaneous disorders (cutaneous T-cell lymphoma and basal-cell carcinoma) and attempt to integrate these new findings into novel pathophysiologic models for two inflammatory dermatoses (rhus dermatitis and psoriasis).
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影响因子:
--
作者:
G. Fierlbeck;G. Rassner;C. Müller
通讯作者:
G. Fierlbeck;G. Rassner;C. Müller
DOI:
10.1111/1523-1747.ep12476441
发表时间:
1988
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
Sackstein,R;Falanga,V;Streilein,JW;Chin,YH
通讯作者:
Chin,YH
影响因子:
10.3
作者:
M. Heng;S. Allen;D. Chase
通讯作者:
D. Chase
DOI:
10.1016/0022-202x(89)90193-0
发表时间:
1989-05
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
Kay H. Singer;Debbi T. Tuck;Hugh A. Sampson;Russell P. Hall
通讯作者:
Kay H. Singer;Debbi T. Tuck;Hugh A. Sampson;Russell P. Hall
影响因子:
--
作者:
Nickoloff,BJ
通讯作者:
Nickoloff,BJ