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人类自然杀伤细胞成熟缺陷支持体内 CD56(bright) 到 CD56(dim) 谱系的发育。

Human natural killer cell maturation defect supports in vivo CD56(bright) to CD56(dim) lineage development.

机构信息

Laboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biología y Medicina Experimental (IBYME), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Buenos Aires, Argentina.

出版信息

PLoS One. 2012;7(12):e51677. doi: 10.1371/journal.pone.0051677. Epub 2012 Dec 11.

Abstract

Two populations of human natural killer (NK) cells can be identified in peripheral blood. The majority are CD3(-)CD56(dim) cells while the minority exhibits a CD3(-)CD56(bright) phenotype. In vitro evidence indicates that CD56(bright) cells are precursors of CD56(dim) cells, but in vivo evidence is lacking. Here, we studied NK cells from a patient that suffered from a melanoma and opportunistic fungal infection during childhood. The patient exhibited a stable phenotype characterized by a reduction in the frequency of peripheral blood CD3(-)CD56(dim) NK cells, accompanied by an overt increase in the frequency and absolute number of CD3(-)CD56(bright) cells. These NK cells exhibited similar expression of perforin, CD57 and CD158, the major activating receptors CD16, NKp46, NKG2D, DNAM-1, and 2B4, as well as the inhibitory receptor CD94/NKG2A, on both CD56(bright) and CD56(dim) NK cells as healthy controls. Also, both NK cell subpopulations produced IFN-γ upon stimulation with cytokines, and CD3(-)CD56(dim) NK cells degranulated in response to cytokines or K562 cells. However, upon stimulation with cytokines, a substantial fraction of CD56(dim) cells failed to up-regulate CD57 and CD158, showed a reduction in the percentage of CD16(+) cells, and CD56(bright) cells did not down-regulate CD62L, suggesting that CD56(dim) cells could not acquire a terminally differentiated phenotype and that CD56(bright) cells exhibit a maturation defect that might result in a potential altered migration pattern. These observations, support the notion that NK cells of this patient display a maturation/activation defect that precludes the generation of mature NK cells at a normal rate accompanied by CD56(dim) NK cells that cannot completely acquire a terminally differentiated phenotype. Thus, our results provide evidence that support the concept that in vivo CD56(bright) NK cells differentiate into CD56(dim) NK cells, and contribute to further understand human NK cell ontogeny.

摘要

两种人群的人类自然杀伤 (NK) 细胞可以在周围血液中识别。大多数是 CD3(-)CD56(dim)细胞,而少数表现出 CD3(-)CD56(bright)表型。体外证据表明,CD56(bright)细胞是 CD56(dim)细胞的前体,但体内证据缺乏。在这里,我们研究了一名患有黑色素瘤和儿童期机会性真菌感染的患者的 NK 细胞。该患者表现出稳定的表型特征,表现为外周血 CD3(-)CD56(dim)NK 细胞频率降低,同时 CD3(-)CD56(bright)细胞频率和绝对数明显增加。这些 NK 细胞在 CD56(bright)和 CD56(dim)NK 细胞上表现出相似的穿孔素、CD57 和 CD158 表达,主要激活受体 CD16、NKp46、NKG2D、DNAM-1 和 2B4,以及抑制受体 CD94/NKG2A,与健康对照者相同。此外,两种 NK 细胞亚群在受到细胞因子刺激时均产生 IFN-γ,CD3(-)CD56(dim)NK 细胞在受到细胞因子或 K562 细胞刺激时脱颗粒。然而,在受到细胞因子刺激时,相当一部分 CD56(dim)细胞未能上调 CD57 和 CD158,CD16(+)细胞的百分比降低,CD56(bright)细胞未能下调 CD62L,表明 CD56(dim)细胞不能获得终末分化表型,CD56(bright)细胞表现出成熟缺陷,可能导致潜在的迁移模式改变。这些观察结果支持这样一种观点,即该患者的 NK 细胞表现出成熟/激活缺陷,阻止了正常速度生成成熟 NK 细胞,同时伴有不能完全获得终末分化表型的 CD56(dim)NK 细胞。因此,我们的结果提供了证据支持这样一种概念,即体内 CD56(bright)NK 细胞分化为 CD56(dim)NK 细胞,并有助于进一步了解人类 NK 细胞的个体发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/3519873/1345d5675bfa/pone.0051677.g004.jpg

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