Toll-like receptor agonists, poly(I:C) and flagellin, lead to IL-36γ induction with divergent release kinetics and differentially alter autophagy in primary human keratinocytes (notice n° 1056838)

détails MARC
000 -LEADER
fixed length control field 02886cam a2200301 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250130132532.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Papayannakos, Christopher J.
Relator term author
245 00 - TITLE STATEMENT
Title Toll-like receptor agonists, poly(I:C) and flagellin, lead to IL-36γ induction with divergent release kinetics and differentially alter autophagy in primary human keratinocytes
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2022.<br/>
500 ## - GENERAL NOTE
General note 29
520 ## - SUMMARY, ETC.
Summary, etc. IL-36γ, a pro-inflammatory member of the IL-1 cytokine superfamily, can be induced and secreted by normal human foreskin keratinocytes (HFKs) in response to pathogenic stimuli, however, the mechanisms underlying the secretion are unknown. In this study, we demonstrate that stimulation with the TLR3 agonist, poly (I:C), led to a delayed secretion of IL-36γ compared to stimulation with the TLR5 agonist, flagellin, despite equal levels of the cytokine ( p = 0.006). IL-36γ was shown to be released from HFKs in its inactive, uncleaved form, based on western blotting. Moreover, recombinant IL-36γ in its activated, cleaved form induced endogenous IL-36γ 10-fold ( p = 0.004) and CXCL8 five-fold ( p = 0.003) over baseline levels compared to unactivated full-length recombinant IL-36γ. The ratio of LC3b-II/LC3b-I was significantly higher in poly(I:C)-treated cells compared to flagellin-treated and unstimulated controls without a change in SQSTM1/p62 after 24 hours of stimulation ( p = 0.043). Under fluorescence microscopy, poly(I:C) led to a two-fold increase at eight hours and four-fold increase at 24 hours in accumulated autophagosomes post-stimulation ( p = 0.032). In contrast, autophagosomes were unchanged relative to baseline in response to flagellin. Bafilomycin A1 treatment enhanced poly(I:C)-mediated IL-36γ secretion ( p = 0.044) while rapamycin led to a noticeable, but non-significant, increase in flagellin-mediated IL-36γ secretion, indicating that interrupting autophagic flux can alter IL-3γ grelease from HFKs. Finally, we show that, compared to clinically normal laryngeal tissue, there were significantly higher levels of LC3b-II in HPV-infected respiratory papilloma tissue, indicating a higher number of autophagosomes; a signature of disrupted autophagic flux.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element autophagy
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element keratinocyte
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element LC3b
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element interleukin-36γ
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element Toll-like receptor
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Zhu, Daniel
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Jung, Bongseok
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Rana, Ali A.
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name DeVoti, James A.
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Abramson, Allan L.
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Bonagura, Vincent R.
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Steinberg, Bettie M.
Relator term author
786 0# - DATA SOURCE ENTRY
Note European Cytokine Network | Volume 33 | 2 | 2022-06-01 | p. 19-29 | 1148-5493
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-european-cytokine-network-2022-2-page-19?lang=en&redirect-ssocas=7080">https://shs.cairn.info/revue-european-cytokine-network-2022-2-page-19?lang=en&redirect-ssocas=7080</a>

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