| Literature DB >> 28065603 |
Sanjeeb Shrestha1, Shin-Yeong Kim1, Young-Jin Yun1, Jun-Kyu Kim2, Jae Man Lee3, Minsang Shin4, Dong-Keun Song1, Chang-Won Hong5.
Abstract
Hypersegmentation of nuclei is considered a distinct characteristic of the antitumoral phenotype of neutrophils. Retinoic acid, a metabolite of retinol, reorganizes and induces segmentation of the nucleus during the differentiation of neutrophils. However, the role of retinoic acid in the phenotype polarization of neutrophils has not been fully established. Here, we investigated the effect of retinoic acid on phenotype polarization of neutrophils. Retinoic acid-induced the hypersegmentation of human neutrophils via retinoic acid receptors and mTOR pathways. Retinoic acid-induced hypersegmented neutrophils enhanced neutrophil extracellular traps (NETs) formation in response to phorbol-12-myristate 13-acetate (PMA) and fMLP (N-Formylmethionine-leucyl-phenylalanine) stimulation, and increased cytotoxicity against various tumor cells. Moreover, retinoic acid treatment attenuated tumor growth in a murine model of tumor. Taken together, these results suggests that retinoic acid induces the phenotype polarization of neutrophils to exert antitumor effects.Entities:
Keywords: Cytotoxicity; Neutrophils; Phenotype; Polarization; Retinoic acid
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Year: 2017 PMID: 28065603 DOI: 10.1016/j.imlet.2017.01.001
Source DB: PubMed Journal: Immunol Lett ISSN: 0165-2478 Impact factor: 3.685