IndraLab

Statements


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"The loss of function mutation in TNFAIP3, an inhibitor of NF-kB activation, in HA20 increased priming of NLRP3 inflammasome [30]."

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"High glucose culturing conditions increased TLR4 and NLRP3 proteins, which were also increased by TNFAIP3 siRNA."

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"Compared with LPS group, TA treatment significantly decreased the mRNA abundance of Bcl2l11, Nlrp3, interleukin-18 receptor 1 precursor (Il18r1), Traf5, Tnfaip3, Ccndbp1, Nfkbia, Casp1, and Cdkn1a whi[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"In mice, the overexpression of TNFAIP3 inhibits NLRP3 inflammasome complex, preventing lupus inflammation and renal injury ( 53 )."

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"On the other hand, TNFAIP3 overexpression significantly alleviates inflammatory responses and reduces activation of NF-κB and the NLRP3 inflammasome ( Li et al., 2015 )."

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"TNFaIP3 prevents the NFκB-dependent upregulation of NLRP3 and conversion of pro-IL1β to mature IL1β through the binding of its A20-like zinc finger domain to ubiquitin chains [52]."

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"In murine models, A20 and Tnfaip3 was shown to downregulate the activity of NLRP3 inflammasome."

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"The staining of NLRP3 positive clusters in CMECs transfected into Len-TNFAIP3 supports these data ( Fig. 7 J–K, P < 0.05), Indicating that the up-regulated TNFAIP3 inhibits NLRP3 activation and IL-1β [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"