Academic Journal
Tyrphostin AG126 Exerts Neuroprotection in CNS Inflammation by a Dual Mechanism
| العنوان: | Tyrphostin AG126 Exerts Neuroprotection in CNS Inflammation by a Dual Mechanism |
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| المؤلفون: | Menzfeld, Christiane, John, Michael, van Rossum, Denise, Regen, Tommy, Scheffel, Joerg, Janova, Hana, Goetz, Alexander A., Ribes, Sandra, Nau, Roland, Borisch, Angela, Boutin, Philippe, Neumann, Konstantin, Bremes, Vanessa, Wienands, Juergen, Reichardt, Holger Michael, Luehder, Fred, Tischner, Denise, Waetzig, Vicky, Herdegen, Thomas, Teismann, Peter, Greig, Iain, Mueller, Michael, Pukrop, Tobias, Mildner, Alexander, Kettenmann, Helmut, Brueck, Wolfgang, Prinz, Marco R., Rotshenker, Shlomo, Weber, Martin S., Hanisch, Uwe-Karsten |
| بيانات النشر: | Wiley-blackwell |
| سنة النشر: | 2015 |
| المجموعة: | Georg-August-Universität Göttingen: GoeScholar |
| الوصف: | The putative protein tyrosine kinase (PTK) inhibitor tyrphostin AG126 has proven beneficial in various models of inflammatory disease. Yet molecular targets and cellular mechanisms remained enigmatic. We demonstrate here that AG126 treatment has beneficial effects in experimental autoimmune encephalomyelitis (EAE), a model for multiple sclerosis. AG126 alleviates the clinical symptoms, diminishes encephalitogenic Th17 differentiation, reduces inflammatory CNS infiltration as well as microglia activation and attenuates myelin damage. We show that AG126 directly inhibits Bruton's tyrosine kinase (BTK), a PTK associated with B cell receptor and Toll-like receptor (TLR) signaling. However, BTK inhibition cannot account for the entire activity spectrum. Effects on TLR-induced proinflammatory cytokine expression in microglia involve AG126 hydrolysis and conversion of its dinitrile side chain to malononitrile (MN). Notably, while liberated MN can subsequently mediate critical AG126 features, full protection in EAE still requires delivery of intact AG126. Its anti-inflammatory potential and especially interference with TLR signaling thus rely on a dual mechanism encompassing BTK and a novel MN-sensitive target. Both principles bear great potential for the therapeutic management of disturbed innate and adaptive immune functions. GLIA 2015;63:1083-1099 |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | unknown |
| تدمد: | 1098-1136 0894-1491 25731696 |
| Relation: | https://resolver.sub.uni-goettingen.de/purl?gro-2/37056; 000353244400011 |
| DOI: | 10.1002/glia.22803 |
| الاتاحة: | https://resolver.sub.uni-goettingen.de/purl?gro-2/37056 https://doi.org/10.1002/glia.22803 |
| رقم الانضمام: | edsbas.70E8E649 |
| قاعدة البيانات: | BASE |
| تدمد: | 10981136 08941491 25731696 |
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| DOI: | 10.1002/glia.22803 |