2017
Lipopolysaccharide treatment of schwannoma cells induced acute elevation of inflammatory mediators
KOHOUTKOVÁ, Marcela; Andrea KORIMOVÁ a Petr DUBOVÝZákladní údaje
Originální název
Lipopolysaccharide treatment of schwannoma cells induced acute elevation of inflammatory mediators
Autoři
KOHOUTKOVÁ, Marcela; Andrea KORIMOVÁ a Petr DUBOVÝ
Vydání
Morphology 2017 50th International Congress of the Czech Anatomical Society 54th Lojda Symposium in Histochemistry, 2017, 2017
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30103 Neurosciences
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/17:00100720
Organizační jednotka
Lékařská fakulta
ISBN
978-80-263-1315-1
Klíčová slova česky
Lipopolysaccharid; Schwannova buňka; neurozánět
Klíčová slova anglicky
Lipopolysaccharide; Schwann cell; neuroinflammation
Změněno: 5. 12. 2018 10:12, prof. RNDr. Petr Dubový, CSc.
Anotace
V originále
Lipopolysaccharide treatment of schwannoma cells induced acute elevation of inflammatory mediators Kohoutková M. (1), Korimová A. (1), Dubový P. (1) (1) Department of Anatomy, Faculty of Medicine, Masaryk University, Brno, Czech Republic Wallerian degeneration is a process of stereotypical reactions of Schwann cells which is important prerequisite for reparation of the damage nerve. Inflammatory activation of Schwann cells can be triggered by endogenous ligands produced during Wallerian degeneration or exogenous pathological molecules via Toll-like receptors (TLRs) [1,2]. Lipopolysaccharide (LPS) was used as a prototypical ligand for activation intracellular immune response of schwannoma cells. Acute inflammatory response of schwannoma cells is associated with increased production of cytokines and transcription factors [3]. We studied proteins the most often associated with inflammation – STAT3 and IL-6 and receptor TLR4, which can transduce inflammatory signal to cell. Rat schwannoma cells (RT4-D6P2T) were treated with LPS (10ng/ml) for 1 hour to induce acute inflammatory responses. TLR4, pSTAT3 and IL-6 proteins were studied by immunocytochemistry and Western blot analysis. We observed dynamic changes of TLR4 deposits in the cell cytoplasm but not in the cell surface. LPS treatment induced enlarging of early endosomes in schwannoma cells. We also found significantly increased levels of pSTAT3 and IL-6 proteins after LPS treatment indicating their crucial role in the induction of inflammation cascade in Schwann cells. [1] S. Rotshenker, Wallerian degeneration: the innate-immune response to traumatic nerve injury., J. Neuroinflammation. 8 (2011) 109. [2] E. Ydens, G. Lornet, V. Smits, S. Goethals, V. Timmerman, S. Janssens, The neuroinflammatory role of Schwann cells in disease, Neurobiol. Dis. 55 (2013) 95–103. [3] H.N. Hao, J.D. Peduzzi-Nelson, P.J. VandeVord, K. Barami, S.P. DeSilva, D. Pelinkovic, L.G. Morawa, Lipopolysaccharide-induced inflammatory cytokine production by Schwann’s cells dependent upon TLR4 expression, J. Neuroimmunol. 212 (2009) 26– 34. Supported by grant 16-08508S of The Czech Science Foundation.
Návaznosti
| GA16-08508S, projekt VaV |
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