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自然杀伤细胞发育与成熟的再探讨:一种新型独特的Lin⁻CD34⁻DNAM-1⁺CXCR4⁺细胞祖细胞的潜在影响

Natural Killer Cell Development and Maturation Revisited: Possible Implications of a Novel Distinct LinCD34DNAM-1CXCR4 Cell Progenitor.

作者信息

Bozzano Federica, Marras Francesco, De Maria Andrea

机构信息

Department of Experimental Medicine (DIMES), University of Genova, Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genova, Genova, Italy.

Istituto Giannina Gaslini , Genova , Italy.

出版信息

Front Immunol. 2017 Mar 9;8:268. doi: 10.3389/fimmu.2017.00268. eCollection 2017.

Abstract

Since the first description of natural killer (NK) cells, the view on their role in innate immunity has evolved considerably. In addition to first-line defense against transformed and pathogen-infected autologous cells, NK cells contribute to modulate adaptive immune responses and in some cases acquire specialized functions, including exhausted, adaptive, and decidual NK cells. NK cells derive from CD34 progenitors, and ; however, it is unclear whether the high phenotype diversity may be generated from these precursors alone. The recent characterization of a novel CD34DNAM-1CXCR4 precursor giving rise to apparently licensed and functional maturing NK cells may suggest the possibility for a higher than expected common lymphocyte precursor diversity and a consequently higher peripheral NK cell phenotype variability. Here, we review the evidences on NK cell central and peripheral development from CD34 precursors and propose a possible updated reading frame based on the characterization of CD34DNAM-1CXCR4 cell progenies, which favors the possibility of concurrent NK cell maturation from different CD34 precursors.

摘要

自从首次描述自然杀伤(NK)细胞以来,人们对其在固有免疫中作用的看法已发生了很大演变。除了对转化细胞和病原体感染的自体细胞进行一线防御外,NK细胞还有助于调节适应性免疫反应,并且在某些情况下会获得特殊功能,包括耗竭性NK细胞、适应性NK细胞和蜕膜NK细胞。NK细胞源自CD34祖细胞,然而,目前尚不清楚仅从这些前体细胞是否就能产生高度的表型多样性。最近对一种新型CD34DNAM-1CXCR4前体细胞的鉴定,该前体细胞可产生明显已获许可且具有功能的成熟NK细胞,这可能表明存在比预期更高的常见淋巴细胞前体多样性,进而导致外周NK细胞表型变异性更高。在此,我们回顾了关于从CD34前体细胞发育为NK细胞的中枢和外周发育的证据,并基于CD34DNAM-1CXCR4细胞后代的特征提出了一个可能的更新读框,该读框支持不同CD34前体细胞同时成熟为NK细胞的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f365/5343008/d3f3f8e1e130/fimmu-08-00268-g001.jpg

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