The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Tumor-derived exosomes regulate expression of immune function-related genes in human T cell subsets
Open accessAbstract
Tumor cell-derived exosomes (TEX) suppress functions of immune cells. Here, changes in the gene profiles of primary human T lymphocytes exposed in vitro to exosomes were evaluated. CD4+ Tconv, CD8+ T or CD4+ CD39+ Treg were isolated from normal donors’ peripheral blood and co-incubated with TEX or exosomes isolated from supernatants of cultured dendritic cells (DEX). Expression levels of 24–27 immune response-related genes in these T cells were quantified by qRT-PCR. In activated T cells, TEX and DEX up-regulated mRNA expression levels of multiple genes. Multifactorial data analysis of ΔCt values identified T cell activation and the immune cell type, but not exosome source, as factors regulating gene expression by exosomes. Treg were more sensitive to TEX-mediated effects than other T cell subsets. In Treg, TEX-mediated down-regulation of genes regulating the adenosine pathway translated into high expression of CD39 and increased adenosine production. TEX also induced up-regulation of inhibitory genes in CD4+ Tconv, which translated into a loss of CD69 on their surface and a functional decline. Exosomes are not internalized by T cells, but signals they carry and deliver to cell surface receptors modulate gene expression and functions of human T lymphocytes.
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Extracellular vesicles: Exosomes, microvesicles, and friends
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Self-citationImmune evasion mediated by PD-L1 on glioblastoma-derived extracellular vesicles
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Metadata
- Authors
- Muller, L., Mitsuhashi, M., Simms, P., Gooding, W. E., & Whiteside, T. L.
- Venue
- Scientific Reports
- Published
- 2016-02-04
- Volume
- 6
- Issue
- 1
- Pages
- 20254-20254
- ISSN
- 2045-2322 (ISSN-L)
- OpenAlex
- W2403293254
- Cited by
- 309
- References
- 6
- FWCI
- 20.77
- Type
- journal article
- Language
- en
- Open access
- gold
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