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Memory like NK cells display stem cell like properties after Zika virus infection

ABSTRACT: Memory like NK cells display stem cell like properties after Zika virus infection

PROVIDER: PRJNA625709 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR11554155_1.fastq.gz	Fastqsanger.gz
	SRR11554155_2.fastq.gz	Fastqsanger.gz
	SRR11554156_1.fastq.gz	Fastqsanger.gz
	SRR11554156_2.fastq.gz	Fastqsanger.gz
	SRR11554157_1.fastq.gz	Fastqsanger.gz

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Memory like NK cells display stem cell like properties after Zika virus infection

Project description:In this study, we show that CD27+ memory like NK cells generated following Zika virus infection exhibited stem-like features viz., self-renewal pathway, differentiation into effector cells and longer telomeres, and greater therapeutic potential than CD27- and naive CD27+ NK cells when adoptively transferred to Zika virus infected mice. In addition, epigenetic landscape of CD27+ memory like NK is markedly different compared to CD27- NK cells.

2020-12-11 | GSE148780 | GEO

Memory like NK cells display stem cell like properties after Zika virus Infection

Project description:Here we show that Zika virus infection induces memory like NK cells that express CD27. This subset shared transcriptional changes with memory CD8 T cells, stem cells and stem like T cells. These NK cells with memory and stemness features which we term NK memory stem cells (SCMNK) demonstrated greater antiviral potential. Transcriptional data of SCMNK and non-memory NK cells is presented.

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Memory like NK cells display stem cell like properties after Zika virus Infection

Project description:Memory like NK cells display stem cell like properties after Zika virus Infection

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Memory like NK cells display stem cell like properties after Zika virus infection.

Project description:NK cells have been shown to display adaptive traits such as memory formation akin to T and B lymphocytes. Here we show that Zika virus infection induces memory like NK cells that express CD27. Strikingly, these cells exhibit stem-like features that include expansion capacity, self-renewal pathway, differentiation into effector cells, longer telomeres and gene signature associated with hematopoietic stem cell (HSC) progenitors. This subset shared transcriptional and epigenetic changes with memory CD8 T cells, stem cells and stem like T cells. These NK cells with memory and stem cell features, which we term "NK memory stem cells", demonstrated greater antiviral potential than CD27- or naïve CD27+ NK when adoptively transferred to Zika infected mice. Our results also suggest a role for the transcription factor TCF-1 in memory and stemness features of this NK subset. This study defines a unique TCF1hi CD27+ NK subset with memory capacity and stem cell features that play a role in antiviral immunity.

| S-EPMC7793296 | biostudies-literature

Quantitative proteomics of cytokine-induced memory-like (CIML) NK cells

Project description:NK cells from healthy donors were isolated from peripheral blood and stimulated overnight with IL-12/15/18 to induce a memory-like phenotype. After 7 days of culture, the phenotype and degranulation potential of CIML NK cells was characterized in two distinct NK cell subsets: CD16+/CD56+ and CD16−/CD56. Finally, NK cell subsets were purified using fluorescence-activated cell sorting (FACS) and subjected to high-throughput multiplexed quantitative proteomics.

2025-07-14 | PXD059190 | Pride

RNA expression of memory NK subsets

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RNA expression of memory NK subsets

Project description:RNA expression of memory NK subsets

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Cytokine induced NK memory transcriptional profile characterization

Project description:By comparing CD94-CD56dim NK cell with or without primary stimulation treatment after 5 days, cytokine induced NK memory related molecules were identified.

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Cytokine induced NK memory transcriptional profile characterization

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CITE-seq of in vitro control and memory-like human NK cells

Project description:Peripheral blood NK cells were cultured into either control or cytokine-induced memory-like NK cells as described in PMID: 32614951. After differentiation, cells were labeled with hashtag antibodies and cite-seq antibodies and control and memory-like NK cells were combined and loaded onto the 10x Genomics Chromium Instrument a the McDonnell Genome Institute at Washington University School of Medicine. The following samples were analyzed to develop a classification tool for unbiased identification of memory-like NK cells in a bulk single-cell RNA-seq population.

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