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鼠 Schnurri-2 控制自然杀伤细胞功能和淋巴瘤发展。

Murine Schnurri-2 controls natural killer cell function and lymphoma development.

机构信息

Department of Immunology, Graduate School of Medicine, Chiba University, Chuo-ku, Chiba, Japan.

出版信息

Leuk Lymphoma. 2012 Mar;53(3):479-86. doi: 10.3109/10428194.2011.625099. Epub 2011 Nov 25.

Abstract

Schnurri (Shn)-2 is a large zinc finger-containing protein implicated in cell growth, signal transduction and lymphocyte development. Here, we report that Shn-2-deficient (Shn-2(-/-)) mice develop CD3-positive lymphoma spontaneously. In Shn-2(-/-) mice, we observed decreased cytotoxicity of natural killer (NK) cells accompanied by decreased expression of perforin and granzyme-B. In addition, phosphorylation of signal transducer and activator of transcription (STAT) 5 was reduced in Shn-2(-/-) NK cells, while phosphorylation of STAT3 and protein expression of nuclear factor-κB p65 subunit were enhanced in Shn-2(-/-) NK cells. Moreover, cell-surface expression of activation molecules such as CD27, CD69 and CD122 were decreased on Shn-2(-/-) NK cells. Thus, Shn-2 is considered to play an important role in the activation and function of NK cells and the development of T cell lymphoma in vivo.

摘要

Schnurri (Shn)-2 是一种含有大量锌指的蛋白质,参与细胞生长、信号转导和淋巴细胞发育。在这里,我们报告 Shn-2 缺陷(Shn-2(-/-))小鼠会自发地发展为 CD3 阳性淋巴瘤。在 Shn-2(-/-)小鼠中,我们观察到自然杀伤(NK)细胞的细胞毒性降低,同时穿孔素和颗粒酶-B 的表达减少。此外,Shn-2(-/-)NK 细胞中信号转导和转录激活因子(STAT)5 的磷酸化减少,而 STAT3 的磷酸化和核因子-κB p65 亚单位的蛋白表达在 Shn-2(-/-)NK 细胞中增强。此外,Shn-2(-/-)NK 细胞表面表达的激活分子,如 CD27、CD69 和 CD122 减少。因此,Shn-2 被认为在 NK 细胞的激活和功能以及体内 T 细胞淋巴瘤的发展中发挥重要作用。

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