Characterization of the altered cutaneous reactivity of transgenic mice whose keratinocytes overexpress B7-1.
Characterization of the altered cutaneous reactivity of transgenic mice whose keratinocytes overexpress B7-1.
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角质形成细胞过度表达 B7-1 的转基因小鼠皮肤反应性改变的表征。
DOI:
10.1006/clin.1997.4491
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发表时间:
1998
期刊:
影响因子:
--
通讯作者:
R. Barth
中科院分区:
文献类型:
--
作者:
A. Gaspari;R. Burns;S. Kondo;A. Nasir;A. Kurup;D. Mlodynia;D. Sauder;R. Barth
B7-1 (CD80) is a second signal molecule usually associated with "professional" APCs that prevents the induction of T-cell clonal anergy and induces IL-2 production during antigen presentation. Tg mice whose epidermal KC overexpress B7-1 exhibit exaggerated and persistent CHS to a variety of haptens that lasts up to 8 weeks after hapten challenge. These Tg mice also exhibit significantly enhanced ear-swelling responses to irritants that are not persistent. Exaggerated CHS was not reflected in the draining lymph node. T-lymphocyte proliferative responses after sensitization and local challenge with haptens, as there were no significant differences between the B7-1 Tg and the NTg mice. However, RT-PCR analysis of mouse ear skin at the hapten challenge site indicated that B7-1 Tg mice had an alteration in the kinetics of in situ lymphokine transcripts compared to NTg mice: IFN-gamma transcripts were first detectable in Tg mouse skin at 2 weeks versus 24 h for NTg mice. RNase protection assays to detect inflammatory cytokine transcripts at hapten application sites indicated that B7-1 Tg mice responded to hapten application with increased TNF-alpha, IL-6, and TNF-beta transcripts compared to NTg mice. Thus, hapten-induced ear swelling in these Tg mice may be mediated by enhanced inflammatory cytokines during the early phase (1-14 days). IFN-gamma-producing lymphocytes may be responsible for the late phase of the ear-swelling response (14-42 days). These data indicate that B7-1 overexpression by KC in mouse skin directly or indirectly affects the nature of cutaneous inflammation induced by haptens and irritants.
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DOI:
10.1172/jci117411
发表时间:
1994
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Nasir,A;Ferbel,B;Salminen,W;Barth,RK;Gaspari,AA
通讯作者:
Gaspari,AA
DOI:
10.1111/1523-1747.ep12365917
发表时间:
1993
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
Matsue,H;CruzJr,PD;Bergstresser,PR;Takashima,A
通讯作者:
Takashima,A
DOI:
10.1073/pnas.91.26.12780
发表时间:
1994
影响因子:
11.1
作者:
Williams,IR;Ort,RJ;Kupper,TS
通讯作者:
Kupper,TS
DOI:
--
发表时间:
1992
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Norton,SD;Zuckerman,L;Urdahl,KB;Shefner,R;Miller,J;Jenkins,MK
通讯作者:
Jenkins,MK
DOI:
10.1073/pnas.90.23.11182
发表时间:
1993
影响因子:
11.1
作者:
Razi-Wolf,Z;Galvin,F;Gray,G;Reiser,H
通讯作者:
Reiser,H