共 29 条
TRAIL: not just for tumors anymore?
被引:29
作者:

Benedict, Chris A.
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h-index: 0
机构:
La Jolla Inst Allergy & Immunol, Div Immune Regulat, La Jolla, CA 92037 USA La Jolla Inst Allergy & Immunol, Div Immune Regulat, La Jolla, CA 92037 USA

Ware, Carl F.
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h-index: 0
机构:
Sanford Burnham Med Res Inst, Infect & Inflammatory Dis Ctr, Lab Mol Immunol, La Jolla, CA 92037 USA La Jolla Inst Allergy & Immunol, Div Immune Regulat, La Jolla, CA 92037 USA
机构:
[1] La Jolla Inst Allergy & Immunol, Div Immune Regulat, La Jolla, CA 92037 USA
[2] Sanford Burnham Med Res Inst, Infect & Inflammatory Dis Ctr, Lab Mol Immunol, La Jolla, CA 92037 USA
基金:
美国国家卫生研究院;
关键词:
APOPTOSIS-INDUCING LIGAND;
PULMONARY ARTERIAL-HYPERTENSION;
SMOOTH-MUSCLE-CELLS;
INFLUENZA-VIRUS;
TNF;
NECROSIS;
RECEPTOR;
MICE;
INFLAMMATION;
IDENTIFICATION;
D O I:
10.1084/jem.20122235
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Since the discovery of TNF-related apoptosis-inducing ligand (TRAIL) and its network of receptors, the majority of attention has focused on the clinical potential of manipulating this pathway in cancer therapy. However, the widespread expression of TRAIL under inflammatory conditions and the ability to induce both apoptotic and prosurvival signaling pathways has suggested that TRAIL plays broader roles in regulating immune processes. Two new studies now show that expression of TRAIL by neutrophils in the lung facilitates defenses against bacterial pathogens, whereas expression of TRAIL by cells within arterioles exacerbates vascular disease. These differentiating results highlight that the context of TRAIL signaling can determine whether the outcome is beneficial or pathogenic for the host.
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页码:1903 / 1906
页数:4
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Crossman, David C.
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Univ E Anglia, Norwich Med Sch, Norwich NR4 7TJ, Norfolk, England Univ Sheffield, Dept Cardiovasc Sci, Sheffield S10 2RX, S Yorkshire, England

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Univ Sheffield, Dept Cardiovasc Sci, Sheffield S10 2RX, S Yorkshire, England Univ Sheffield, Dept Cardiovasc Sci, Sheffield S10 2RX, S Yorkshire, England
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