Anti-Hu antibodies activate enteric and sensory neurons

IgG of type 1 anti-neuronal nuclear antibody (ANNA-1, anti-Hu) specificity is a serological marker of paraneoplastic neurological autoimmunity (including enteric/autonomic) usually related to small-cell lung carcinoma. We show here that IgG isolated from such sera and also affinity-purified anti-HuD...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Li Qin
Michel Klaus
Annaházi Anita
Demir Ihsan E.
Ceyhan Güralp O.
Zeller Florian
Komorowski Lars
Stöcker Winfried
Beyak Michael J.
Grundy David
Farrugia Gianrico
De Giorgio Roberto
Schemann Michael
Dokumentumtípus: Cikk
Megjelent: 2016
Sorozat:SCIENTIFIC REPORTS 6 No. 1
Tárgyszavak:
doi:10.1038/srep38216

mtmt:35735080
Online Access:http://publicatio.bibl.u-szeged.hu/40312
Leíró adatok
Tartalmi kivonat:IgG of type 1 anti-neuronal nuclear antibody (ANNA-1, anti-Hu) specificity is a serological marker of paraneoplastic neurological autoimmunity (including enteric/autonomic) usually related to small-cell lung carcinoma. We show here that IgG isolated from such sera and also affinity-purified anti-HuD label enteric neurons and cause an immediate spike discharge in enteric and visceral sensory neurons. Both labelling and activation of enteric neurons was prevented by preincubation with the HuD antigen. Activation of enteric neurons was inhibited by the nicotinic receptor antagonists hexamethonium and dihydro-β-erythroidine and reduced by the P2X antagonist pyridoxal phosphate-6-azo (benzene-2,4-disulfonic acid (PPADS) but not by the 5-HT 3 antagonist tropisetron or the N-type Ca-channel blocker ω-Conotoxin GVIA. Ca ++ imaging experiments confirmed activation of enteric neurons but not enteric glia. These findings demonstrate a direct excitatory action of ANNA-1, in particular anti-HuD, on visceral sensory and enteric neurons, which involves nicotinic and P2X receptors. The results provide evidence for a novel link between nerve activation and symptom generation in patients with antibody-mediated gut dysfunction.
Terjedelem/Fizikai jellemzők:12
ISSN:2045-2322