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TCRJα18种系敲除小鼠中黏膜相关恒定T细胞的缺陷

Deficiency of Mucosal-Associated Invariant T Cells in TCRJα18 Germline Knockout Mice.

作者信息

Xie Jinhai, Pan Yun, Tao Huishan, Wang Peng, Chen Yongping, Gao Jimin, Zhong Xiao-Ping

机构信息

Division of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC 27710.

School of Laboratory Medicine, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.

出版信息

Immunohorizons. 2019 Jun 11;3(6):203-207. doi: 10.4049/immunohorizons.1900035.

Abstract

Mucosal-associated invariant T (MAIT) cells and invariant NK T (iNKT) cells account for the major lymphocyte populations that express invariant TCRα-chains. MAIT cells mostly express the TCRVα19-Jα33 TCR in mice and the TCRVα7.2-Jα33 TCR in humans, whereas iNKT cells express the TCRVα14-Jα18 TCR in mice and the TCRVα24-Jα18 TCR in humans. Both MAIT and iNKT cells have the capacity to quickly produce a variety of cytokines in response to agonist stimuli and to regulate both innate and adaptive immunity. The germline TCRJα18 knockout ( ) mice have been used extensively for studying iNKT cells. Although it has been reported that the TCRα repertoire was narrowed and the level of transcript was decreased in this strain of mice, direct assessment of MAIT cells in these mice has not been reported. We demonstrate in this study that this strain of mice is also defective of MAIT T cells, cautioning data interpretation when using this strain of mice.

摘要

黏膜相关恒定T(MAIT)细胞和恒定自然杀伤T(iNKT)细胞是表达恒定TCRα链的主要淋巴细胞群体。在小鼠中,MAIT细胞大多表达TCRVα19-Jα33 TCR,在人类中则表达TCRVα7.2-Jα33 TCR;而iNKT细胞在小鼠中表达TCRVα14-Jα18 TCR,在人类中表达TCRVα24-Jα18 TCR。MAIT细胞和iNKT细胞都有能力在受到激动剂刺激后迅速产生多种细胞因子,并调节固有免疫和适应性免疫。种系TCRJα18基因敲除小鼠已被广泛用于研究iNKT细胞。尽管已有报道称该品系小鼠的TCRα库变窄且转录水平降低,但尚未见对这些小鼠中MAIT细胞的直接评估报道。我们在本研究中证明,该品系小鼠的MAIT T细胞也存在缺陷,这提醒在使用该品系小鼠时要谨慎解读数据。

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