Dorzolamide suppresses PKCδ -TIRAP-p38 MAPK signaling axis to dampen the inflammatory response

Sepsis is a syndrome due to microbial infection causing impaired multiorgan function. Its underlying cause is immune dysfunction and macrophages play an essential role. TIRAP interaction with PKCδ in macrophage was studied, revealing downstream signaling by Western blot and quantitative reverse tran...

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Veröffentlicht in:Future medicinal chemistry 2023-04, Vol.15 (6), p.533-554
Hauptverfasser: Rajpoot, Sajjan, Kumar, Ashutosh, Gaponenko, Vadim, Thurston, Teresa Lm, Mehta, Dolly, Faisal, Syed M, Zhang, Kam Yj, Jha, Hem C, Darwhekar, Gajanan N, Baig, Mirza S
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Sprache:eng
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Zusammenfassung:Sepsis is a syndrome due to microbial infection causing impaired multiorgan function. Its underlying cause is immune dysfunction and macrophages play an essential role. TIRAP interaction with PKCδ in macrophage was studied, revealing downstream signaling by Western blot and quantitative reverse transcriptase PCR. Dorzolamide (DZD) disrupting TIRAP–PKCδ interaction was identified by virtual screening and validated and in septic mice. The study highlights the indispensable role of TIRAP–PKCδ in p38 MAPK-activation, NF-κB- and AP-1-mediated proinflammatory cytokines expression, whereas DZD significantly attenuated the signaling. Targeting TIRAP–PKCδ interaction by DZD is a novel therapeutic approach for treating sepsis.
ISSN:1756-8919
1756-8927
DOI:10.4155/fmc-2022-0260