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Tumor-Derived Small Extracellular Vesicles Induce Pro-Inflammatory Cytokine Expression and PD-L1 Regulation in M0 Macrophages via IL-6/STAT3 and TLR4 Signaling Pathways

Title: Tumor-Derived Small Extracellular Vesicles Induce Pro-Inflammatory Cytokine Expression and PD-L1 Regulation in M0 Macrophages via IL-6/STAT3 and TLR4 Signaling Pathways
Authors: Marzia Pucci; Stefania Raimondo; Ornella Urzì; Marta Moschetti; Maria Antonietta Di Bella; Alice Conigliaro; Nadia Caccamo; Marco Pio La Manna; Simona Fontana; Riccardo Alessandro
Source: International Journal of Molecular Sciences, Vol 22, Iss 12118, p 12118 (2021)
Publisher Information: MDPI AG
Publication Year: 2021
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: small extracellular vesicles; M0 macrophages; PD-L1; TLR4; colorectal cancer; multiple myeloma; Biology (General); QH301-705.5; Chemistry; QD1-999
Description: Tumor-associated macrophages play a key role in promoting tumor progression by exerting an immunosuppressive phenotype associated with the expression of programmed cell death ligand 1 (PD-L1). It is well known that tumor-derived small extracellular vesicles (SEVs) affect the tumor microenvironment, influencing TAM behavior. The present study aimed to examine the effect of SEVs derived from colon cancer and multiple myeloma cells on macrophage functions. Non-polarized macrophages (M0) differentiated from THP-1 cells were co-cultured with SEVs derived from a colorectal cancer (CRC) cell line, SW480, and a multiple myeloma (MM) cell line, MM1.S. The expression of PD-L1, interleukin-6 (IL-6), and other inflammatory cytokines as well as of the underlying molecular mechanisms were evaluated. Our results indicate that SEVs can significantly upregulate the expressions of PD-L1 and IL-6 at both the mRNA and protein levels and can activate the STAT3 signaling pathway. Furthermore, we identified the TLR4/NF-kB pathway as a convergent mechanism for SEV-mediated PD-L1 expression. Overall, these preliminary data suggest that SEVs contribute to the formation of an immunosuppressive microenvironment.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1422-0067/22/22/12118; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/b9ed3f2105a84ff789755d2c3f2aa606
DOI: 10.3390/ijms222212118
Availability: https://doi.org/10.3390/ijms222212118; https://doaj.org/article/b9ed3f2105a84ff789755d2c3f2aa606
Accession Number: edsbas.78AC6DE2
Database: BASE