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自然杀伤细胞的扩增需要 HuR 并介导对实体肿瘤和长期病毒感染的控制。

NK cell expansion requires HuR and mediates control of solid tumors and long-term virus infection.

机构信息

Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.

Siteman Cancer Center, Washington University School of Medicine , St. Louis, MO, USA.

出版信息

J Exp Med. 2023 Nov 6;220(11). doi: 10.1084/jem.20231154. Epub 2023 Sep 12.

Abstract

Natural killer (NK) cells are lymphocytes capable of controlling tumors and virus infections through direct lysis and cytokine production. While both T and NK cells expand and accumulate in affected tissues, the role of NK cell expansion in tumor and viral control is not well understood. Here, we show that posttranscriptional regulation by the RNA-binding protein HuR is essential for NK cell expansion without negatively affecting effector functions. HuR-deficient NK cells displayed defects in the metaphase of the cell cycle, including decreased expression and alternative splicing of Ska2, a component of the spindle and kinetochore complex. HuR-dependent NK cell expansion contributed to long-term cytomegalovirus control and facilitated control of subcutaneous tumors but not tumor metastases in two independent tumor models. These results show that posttranscriptional regulation by HuR specifically affects NK cell expansion, which is required for the control of long-term virus infection and solid tumors, but not acute infection or tumor metastases, highlighting fundamental differences with antigen-specific T cell control.

摘要

自然杀伤 (NK) 细胞是能够通过直接溶解和细胞因子产生来控制肿瘤和病毒感染的淋巴细胞。虽然 T 细胞和 NK 细胞在受影响的组织中都扩增和积累,但 NK 细胞扩增在肿瘤和病毒控制中的作用尚不清楚。在这里,我们表明 RNA 结合蛋白 HuR 的转录后调节对于 NK 细胞的扩增是必不可少的,而不会对效应功能产生负面影响。HuR 缺陷型 NK 细胞在细胞周期的中期表现出缺陷,包括纺锤体和动粒复合物的组成部分 Ska2 的表达和剪接体减少。HuR 依赖性 NK 细胞扩增有助于长期巨细胞病毒控制,并有助于两种独立的肿瘤模型中皮下肿瘤的控制,但不能控制肿瘤转移。这些结果表明 HuR 的转录后调节特异性影响 NK 细胞的扩增,这对于控制长期病毒感染和实体瘤是必需的,但对于急性感染或肿瘤转移则不是必需的,突出了与抗原特异性 T 细胞控制的根本区别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd0/10497399/a2c081f0b1b9/JEM_20231154_GA.jpg

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