2016
Bovine lactoferrin free of lipopolysaccharide can induce a proinflammatory response of macrophages
ZEMÁNKOVÁ, Naďa, Katarína CHLEBOVÁ, Jan MATIASOVIC, Jana PRODELALOVA, Jan GEBAUER et. al.Základní údaje
Originální název
Bovine lactoferrin free of lipopolysaccharide can induce a proinflammatory response of macrophages
Autoři
ZEMÁNKOVÁ, Naďa (203 Česká republika, domácí), Katarína CHLEBOVÁ (703 Slovensko, domácí), Jan MATIASOVIC, Jana PRODELALOVA, Jan GEBAUER (203 Česká republika, domácí) a Martin FALDYNA (garant)
Vydání
BMC Veterinary Research, London, BMC, 2016, 1746-6148
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
40301 Veterinary science
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 1.750
Kód RIV
RIV/00216224:14310/16:00111639
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000387286300001
Klíčová slova anglicky
Inflammatory cytokines; LPS; NF kappa B; NIK; TLR4
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 5. 2020 10:24, Mgr. Marie Šípková, DiS.
Anotace
V originále
Background: Lactoferrin (LF) is an 80 kDa glycoprotein which is known for its effects against bacteria, viruses and other pathogens. It also has a high potential in nutrition therapy and welfare of people and a variety of animals, including piglets. The ability to bind lipopolysaccharide (LPS) is one of the described anti-inflammatory mechanisms of LF. Previous studies suggested that cells can be stimulated even by LPS-free LF. Therefore, the aim of our study was to bring additional information about this possibility. Porcine monocyte derived macrophages (MDMF) and human embryonic kidney (HEK) cells were stimulated with unpurified LF in complex with LPS and with purified LF without bound LPS. Results: Both cell types were stimulated with unpurified as well as purified LF. On the other hand, neither HEK0 cells not expressing any TLR nor HEK4a cells transfected with TLR4 produced any pro-inflammatory cytokine transcripts after stimulation with purified LF. This suggests that purified LF without LPS stimulates cells via another receptor than TLR4. An alternative, TLR4-independent, pathway was further confirmed by analyses of the NF-kappa-B- inducing kinase (NIK) activation. Western blot analyses showed NIK which activates different NF kappa B subunits compared to LF-LPS signaling via TLR4. Though, this confirmed an alternative pathway which is used by the purified LF free of LPS. This stimulation of MDMF led to low, but significant amounts of pro-inflammatory cytokines, which can be considered as a positive stimulation of the immune system. Conclusion: Our results suggest that LF's ability is not only to bind LPS, but LF itself may be a stimulant of pro-inflammatory pathways.