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由于 ORAI1 中的纯合突变导致的联合免疫缺陷,该突变会删除与 STIM1 相互作用的 C 末端。

Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1.

机构信息

Division of Immunology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Department of Pediatrics, Sultan Qaboos University, Muscat, Oman.

出版信息

Clin Immunol. 2016 May;166-167:100-2. doi: 10.1016/j.clim.2016.03.012. Epub 2016 Apr 6.

Abstract

ORAI1 is the pore-forming subunit of the calcium release-activated calcium channel responsible for calcium influx into cells triggered by endoplasmic reticulum store depletion. We report here a patient with severe combined immunodeficiency and absent store-operated calcium entry due to a novel mutation in ORAI1 that results in the expression of a C-terminally truncated protein that abolishes ORAI1 binding to STIM1.

摘要

ORAI1 是钙释放激活钙通道的孔形成亚基,负责内质网储存耗竭触发的细胞内钙离子内流。我们在此报告一例严重联合免疫缺陷患者,由于 ORAI1 的新突变导致表达截短的 C 端蛋白,从而消除了 ORAI1 与 STIM1 的结合,导致无储存操纵的钙内流。

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