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抗原呈递不足和 Ts 细胞诱导是紫外线照射的不同效应。

Deficient antigen presentation and Ts induction are separate effects of ultraviolet irradiation.

作者信息

Saijo S, Bucana C D, Ramirez K M, Cox P A, Kripke M L, Strickland F M

机构信息

Department of Dermatology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Cell Immunol. 1995 Sep;164(2):189-202. doi: 10.1006/cimm.1995.1161.

Abstract

Ultraviolet-B irradiation of murine skin before contact sensitization alters the antigen-presenting activity of cells in the skin and draining lymph nodes (DLN), decreases the contact hypersensitivity (CHS) response, and induces hapten-specific Ts cells. We determined whether hapten-bearing antigen-presenting cells (APC) from the DLN of UV-irradiated mice induce Ts cells. APC from UV-irradiated, FITC-sensitized mice were isolated, and FITC+ cells were FACS-purified and injected into the hind footpads of naive, syngeneic mice. Unseparated and FACS-purified bright FITC+ cells (FITChi) from UV-irradiated mice induced Ts. However, dull (FITClo) FITC+ cells, T-cell-depleted FITChi cells, or DLN cells from C3H SCID mice failed to induce Ts. Injection of FITC-bearing DLN cells from nonirradiated mice into UV-irradiated recipients failed to immunize and induced Ts instead. Treatment of the UV-irradiated recipients with anti-TNF-alpha blocked these effects. Thus, transferable suppression is due to Thy-1+ cells, does not require UV-altered APC for induction, and may depend on TNF-alpha.

摘要

在接触致敏前对小鼠皮肤进行紫外线B照射,会改变皮肤和引流淋巴结(DLN)中细胞的抗原呈递活性,降低接触性超敏反应(CHS),并诱导半抗原特异性Ts细胞。我们确定了来自紫外线照射小鼠DLN的携带半抗原的抗原呈递细胞(APC)是否能诱导Ts细胞。分离来自紫外线照射、异硫氰酸荧光素(FITC)致敏小鼠的APC,对FITC+细胞进行荧光激活细胞分选(FACS)纯化,并将其注射到同基因的未致敏小鼠的后足垫中。来自紫外线照射小鼠的未分离和FACS纯化的明亮FITC+细胞(FITChi)可诱导Ts细胞。然而,暗淡的(FITClo)FITC+细胞、去除T细胞的FITChi细胞或来自C3H SCID小鼠的DLN细胞均未能诱导Ts细胞。将来自未照射小鼠的携带FITC的DLN细胞注射到紫外线照射的受体中,未能使其免疫,反而诱导了Ts细胞。用抗肿瘤坏死因子-α(TNF-α)处理紫外线照射的受体可阻断这些效应。因此,可转移的抑制作用归因于Thy-1+细胞,诱导过程不需要紫外线改变的APC,且可能依赖于TNF-α。

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