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重新审视肝脏固有 NK 细胞的起源和功能。

Re-examining the origin and function of liver-resident NK cells.

机构信息

Institute of Immunology and CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences and Medical Center, University of Science & Technology of China, Hefei, Anhui 230027, China.

Institute of Immunology and CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences and Medical Center, University of Science & Technology of China, Hefei, Anhui 230027, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, China.

出版信息

Trends Immunol. 2015 May;36(5):293-9. doi: 10.1016/j.it.2015.03.006. Epub 2015 Apr 3.

Abstract

Recent studies have identified a population of liver-resident innate lymphoid cells (ILCs) that, based on the expression of certain phenotypic markers, were termed 'liver-resident NK cells' and considered to be a new subset of conventional natural killer (cNK) cells. However, different transcriptional networks control the development of liver-resident NK cells and cNK cells and, furthermore, these cells exhibit features that characterize mucosal ILC1s. Here, we review findings providing insight into the origin, phenotype, and function of liver-resident NK cells, and discuss these in the context of the current understanding of lineage relations of ILC subsets. We propose that the similarities between liver-resident NK cells and mucosal ILC1s should be considered when revising the categorization framework for these cells, and discuss implications of this revision for other tissue-specific NK cells.

摘要

最近的研究已经确定了一群肝脏驻留固有淋巴细胞 (ILCs),根据某些表型标志物的表达,它们被称为“肝脏驻留 NK 细胞”,并被认为是传统自然杀伤 (cNK) 细胞的一个新亚群。然而,不同的转录网络控制着肝脏驻留 NK 细胞和 cNK 细胞的发育,此外,这些细胞还表现出特征性的黏膜 ILC1 特征。在这里,我们回顾了有关肝脏驻留 NK 细胞的起源、表型和功能的研究结果,并在当前对 ILC 亚群谱系关系的理解的背景下讨论了这些结果。我们提出,在修订这些细胞的分类框架时,应该考虑到肝脏驻留 NK 细胞与黏膜 ILC1 之间的相似性,并讨论这种修订对其他组织特异性 NK 细胞的影响。

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