VEREŠČÁKOVÁ, Hana, Gabriela AMBROŽOVÁ, Lukáš KUBALA, Tomáš PEREČKO, Adolf KOUDELKA, Ondřej VAŠÍČEK, T.K. RUDOLPH, A. KLINKE, S.R. WOODCOCK, B.A. FREEMAN and Michaela PEKAROVÁ. Nitro-oleic acid regulates growth factor-induced differentiation of bone marrow-derived macrophages. Free Radical Biology and Medicine. NEW YORK: ELSEVIER SCIENCE INC, 2017, vol. 104, March, p. 10-19. ISSN 0891-5849. Available from: https://dx.doi.org/10.1016/j.freeradbiomed.2017.01.003.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Nitro-oleic acid regulates growth factor-induced differentiation of bone marrow-derived macrophages
Authors VEREŠČÁKOVÁ, Hana (203 Czech Republic), Gabriela AMBROŽOVÁ (203 Czech Republic), Lukáš KUBALA (203 Czech Republic), Tomáš PEREČKO (703 Slovakia), Adolf KOUDELKA (203 Czech Republic, belonging to the institution), Ondřej VAŠÍČEK (203 Czech Republic), T.K. RUDOLPH (276 Germany), A. KLINKE (276 Germany), S.R. WOODCOCK (840 United States of America), B.A. FREEMAN (840 United States of America) and Michaela PEKAROVÁ (703 Slovakia, guarantor).
Edition Free Radical Biology and Medicine, NEW YORK, ELSEVIER SCIENCE INC, 2017, 0891-5849.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 6.020
RIV identification code RIV/00216224:14310/17:00096042
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.freeradbiomed.2017.01.003
UT WoS 000395968300002
Keywords (in Czech) Nitro-oleic acid; Nitro-fatty acids; Differentiation; Inflammation; Macrophages; Growth factors; Signaling pathways
Keywords in English Nitro-oleic acid; Nitro-fatty acids; Differentiation; Inflammation; Macrophages; Growth factors; Signaling pathways
Tags NZ, rivok
Tags International impact, Reviewed
Changed by Changed by: Ing. Nicole Zrilić, učo 240776. Changed: 9/4/2018 16:41.
Abstract
Many diseases accompanied by chronic inflammation are connected with dysregulated activation of macrophage subpopulations. Recently, we reported that nitro-fatty acids (NO2-FAs), products of metabolic and inflammatory reactions of nitric oxide and nitrite, modulate macrophage and other immune cell functions. Bone marrow cell suspensions were isolated from mice and supplemented with macrophage colony-stimulating factor (M-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF) in combination with NO2-OA for different times. RAW 264.7 macrophages were used for short-term (1-5 min) experiments. We discovered that NO2-OA reduces cell numbers, cell colony formation, and proliferation of macrophages differentiated with colony-stimulating factors (CSFs), all in the absence of toxicity. In a case of GM-CSF-induced bone marrow-derived macrophages (BMMs), NO2-OA acts via downregulation of signal transducer and activator of transcription 5 and extracellular signal-regulated kinase (ERK) activation. In the case of M-CSF-induced BMMs, NO2-OA decreases activation of M-CSFR and activation of related PI3K and ERR. Additionally, NO2-OA also attenuates activation of BMMs. In aggregate, we demonstrate that NO2-OA regulates the process of macrophage differentiation and that NO2-FAs represent a promising therapeutic tool in the treatment of inflammatory pathologies linked with increased accumulation of macrophages in inflamed tissues.
PrintDisplayed: 23/7/2024 17:30