| Literature DB >> 31169450 |
Silvana Sandri1, Cristina Bichels Hebeda1, Rodrigo Azevedo Loiola1, Selma Calgaroto2, Mayara Klimuk Uchiyama3, Koiti Araki3, Luiza Abrahão Frank4, Karina Paese2,4, Silvia Stanisçuaski Guterres4, Adriana Raffin Pohlmann2,4, Sandra Helena Poliselli Farsky1.
Abstract
Aim: Poly(ε-caprolactone) lipid-core nanocapsules (LNCs) are efficient drug carriers and drug-free LNCs display therapeutic effects, inhibiting tumor growth and neutrophil activities. Herein, we investigated the direct actions of LNCs on human immune cells, to guide their therapeutic application. Materials & methods: LNC's uptake, cytokine release, cell migration, proliferation and intracellular pathways under inflammatory stimulation were investigated. Results & conclusion: LNCs quickly penetrated leukocytes without cytotoxicity; inhibited mitogen-induced lymphocyte proliferation, cytokine release and leukocyte migration under inflammatory stimulation, which were associated with inhibition of the MAP kinase pathway and intracellular calcium influx. Hence, we showed LNCs as a down-regulatory agent on immune cells, suggesting that either the particles themselves or their application as a drug carrier can halt non-desired inflammatory processes.Entities:
Keywords: MAPK signaling; cell migration; cytokines release; immunosuppression; peripheral blood mononuclear cells; polymorphonuclear cells
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Year: 2019 PMID: 31169450 DOI: 10.2217/nnm-2018-0484
Source DB: PubMed Journal: Nanomedicine (Lond) ISSN: 1743-5889 Impact factor: 5.307