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肿瘤坏死因子-α(TNF-α)及其受体在正常皮肤和银屑病皮肤中的定位:表皮细胞表达55-kD的TNF受体,但不表达75-kD的TNF受体。

Localization of tumour necrosis factor-alpha (TNF-alpha) and its receptors in normal and psoriatic skin: epidermal cells express the 55-kD but not the 75-kD TNF receptor.

作者信息

Kristensen M, Chu C Q, Eedy D J, Feldmann M, Brennan F M, Breathnach S M

机构信息

Kennedy Institute of Rheumatology, London, UK.

出版信息

Clin Exp Immunol. 1993 Nov;94(2):354-62. doi: 10.1111/j.1365-2249.1993.tb03457.x.

DOI:10.1111/j.1365-2249.1993.tb03457.x
PMID:8222328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1534247/
Abstract

The distribution of TNF-alpha, p55 TNF receptor (TNF-R) and p75 TNF-R in normal skin and uninvolved and lesional skin from psoriasis patients has been investigated, using specific mono- and polyclonal antibodies. In normal skin, and uninvolved and lesional skin from psoriasis patients, p55 TNF-R is associated with epidermal keratinocytes and a network of upper dermal dendritic cells. This suggests that the actions of TNF-alpha on epidermal cells in vivo are mediated by binding to the p55 TNF-R. In lesional psoriasis skin, there was staining of the parakeratotic stratum corneum and increased expression of p55 TNF-R in association with upper dermal blood vessels. Staining for p75 TNF-R in normal skin was restricted to eccrine sweat ducts and dermal dendritic cells, and was absent from the epidermis. In lesional psoriasis skin, there was staining for p75 TNF-R in association with upper dermal blood vessels and perivascular infiltrating cells. TNF-alpha in normal skin was predominantly localized to the basal cell layers of the epidermis, and was seen in association with eccrine ducts and sebaceous glands. In lesional psoriasis skin, and to a lesser extent in uninvolved psoriasis skin, TNF-alpha was distributed throughout the epidermis, and was also specifically localized to upper dermal blood vessels. Up-regulation of TNF-alpha, p55 TNF-R and p75 TNF-R on dermal blood vessels in psoriasis may play an important role in the pathogenesis of this condition by promoting cutaneous recruitment of inflammatory cells.

摘要

运用特异性单克隆和多克隆抗体,对正常皮肤以及银屑病患者未受累皮肤和皮损皮肤中肿瘤坏死因子-α(TNF-α)、p55肿瘤坏死因子受体(TNF-R)和p75 TNF-R的分布情况进行了研究。在正常皮肤以及银屑病患者的未受累皮肤和皮损皮肤中,p55 TNF-R与表皮角质形成细胞以及真皮上层的树突状细胞网络相关联。这表明TNF-α在体内对表皮细胞的作用是通过与p55 TNF-R结合来介导的。在银屑病皮损皮肤中,角化不全的角质层有染色,且p55 TNF-R的表达增加,与真皮上层血管相关。正常皮肤中p75 TNF-R的染色局限于小汗腺导管和真皮树突状细胞,表皮中无染色。在银屑病皮损皮肤中,p75 TNF-R的染色与真皮上层血管和血管周围浸润细胞相关。正常皮肤中的TNF-α主要定位于表皮的基底细胞层,可见于小汗腺导管和皮脂腺。在银屑病皮损皮肤中,以及在程度较轻的未受累银屑病皮肤中,TNF-α分布于整个表皮,并且还特异性定位于真皮上层血管。银屑病中真皮血管上TNF-α、p55 TNF-R和p75 TNF-R的上调可能通过促进炎症细胞向皮肤募集而在该病的发病机制中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/6b9914f500b4/clinexpimmunol00019-0138-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/25b88cd5d1af/clinexpimmunol00019-0136-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/5329e5f1f74e/clinexpimmunol00019-0134-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/50b294d55cf1/clinexpimmunol00019-0137-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/7b22ce891ad0/clinexpimmunol00019-0137-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/6b9914f500b4/clinexpimmunol00019-0138-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/25b88cd5d1af/clinexpimmunol00019-0136-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/f3edf4f49da4/clinexpimmunol00019-0136-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/2d1941ba1f7a/clinexpimmunol00019-0133-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/894730982119/clinexpimmunol00019-0134-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/5329e5f1f74e/clinexpimmunol00019-0134-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/50b294d55cf1/clinexpimmunol00019-0137-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/7b22ce891ad0/clinexpimmunol00019-0137-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dc/1534247/6b9914f500b4/clinexpimmunol00019-0138-a.jpg

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