著作: [北村 明子]/[佐々木 由紀]/Abe Takaya/Kano Hirotsugu/[安友 康二]/An inherited mutation in NLRC4 causes autoinflammation in human and mice./[The Journal of Experimental Medicine]
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種別 | 必須 | 学術論文(審査論文) | |||
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言語 | 必須 | 英語 | |||
招待 | 推奨 | ||||
審査 | 推奨 | ||||
カテゴリ | 推奨 | ||||
共著種別 | 推奨 | ||||
学究種別 | 推奨 | ||||
組織 | 推奨 | ||||
著者 | 必須 | ||||
題名 | 必須 |
(英) An inherited mutation in NLRC4 causes autoinflammation in human and mice. |
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副題 | 任意 | ||||
要約 | 任意 |
(英) Autoinflammatory syndromes cause sterile inflammation in the absence of any signs of autoimmune responses. Familial cold autoinflammatory syndrome (FCAS) is characterized by intermittent episodes of rash, arthralgia, and fever after exposure to cold stimuli. We have identified a missense mutation in the NLRC4 gene in patients with FCAS. NLRC4 has been known as a crucial sensor for several Gram-negative intracellular bacteria. The mutation in NLRC4 in FCAS patients promoted the formation of NLRC4-containing inflammasomes that cleave procaspase-1 and increase production of IL-1. Transgenic mice that expressed mutant Nlrc4 under the invariant chain promoter developed dermatitis and arthritis. Inflammation within tissues depended on IL-1-mediated production of IL-17A from neutrophils but not from T cells. Our findings reveal a previously unrecognized link between NLRC4 and a hereditary autoinflammatory disease and highlight the importance of NLRC4 not only in the innate immune response to bacterial infections but also in the genesis of inflammatory diseases. |
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キーワード | 推奨 |
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発行所 | 推奨 | ||||
誌名 | 必須 |
The Journal of Experimental Medicine([The Rockefeller University Press])
(pISSN: 0022-1007, eISSN: 1540-9538)
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巻 | 必須 | 211 | |||
号 | 必須 | 12 | |||
頁 | 必須 | 2385 2396 | |||
都市 | 任意 | ||||
年月日 | 必須 | 2014年 11月 10日 | |||
URL | 任意 | ||||
DOI | 任意 | 10.1084/jem.20141091 (→Scopusで検索) | |||
PMID | 任意 | 25385754 (→Scopusで検索) | |||
CRID | 任意 | ||||
WOS | 任意 | ||||
Scopus | 任意 | 2-s2.0-84911922142 | |||
評価値 | 任意 | ||||
被引用数 | 任意 | ||||
指導教員 | 推奨 | ||||
備考 | 任意 |
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