Equine bone marrow-derived mesenchymal stromal cells inhibit reactive oxygen species production by neutrophils

•Equine mesenchymal stromal cells inhibit oxidative metabolism in neutrophils and increase their lifespan.•The supernatant obtained from equine mesenchymal stromal cells strongly inhibit respiratory burst of neutrophils.•The supernatant obtained from equine mesenchymal stromal cells doesn’t affect i...

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Veröffentlicht in:Veterinary immunology and immunopathology 2020-03, Vol.221, p.109975-109975, Article 109975
Hauptverfasser: Espinosa, Gabriel, Plaza, Anita, Schenffeldt, Andrés, Alarcón, Pablo, Gajardo, Gonzalo, Uberti, Benjamín, Morán, Gabriel, Henríquez, Claudio
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Sprache:eng
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Zusammenfassung:•Equine mesenchymal stromal cells inhibit oxidative metabolism in neutrophils and increase their lifespan.•The supernatant obtained from equine mesenchymal stromal cells strongly inhibit respiratory burst of neutrophils.•The supernatant obtained from equine mesenchymal stromal cells doesn’t affect important microbicidal functions. Polymorphonuclear neutrophils (PMN) are the largest leukocyte population in the blood of most mammals including horses, and play an important defensive role in many infectious diseases. However, the mechanisms that increase PMN as one of the main cellular subsets in the defense against pathogens could also be involved in the pathophysiology of dysregulated inflammatory conditions. Mesenchymal stem/stromal cells (MSCs) are a heterogeneous population with a modulatory potential on the inflammatory response and are known to interact with nearly all cells of the immune system, including PMN. In this study, the in vitro modulation of equine bone marrow-derived MSCs on equine PMN phagocytosis, ROS production, and NETs generation was assessed. In co-culture with MSCs, unstimulated PMN produce less ROS (2.88 % ± 1.43) than PMN in single culture (5.89 % ± 2.63) (p = 0.016). Moreover, PMN co-cultured with MSCs remain conditioned to produce fewer ROS after PMA stimulation in comparison to PMN in single culture (p 
ISSN:0165-2427
1873-2534
DOI:10.1016/j.vetimm.2019.109975