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Sci Rep. 2017 May 24;7(1):2384. doi: 10.1038/s41598-017-02468-8.

PKC-δ isoform plays a crucial role in Tat-TLR4 signalling pathway to activate NF-κB and CXCL8 production.

Author information

1
CPTP, U1043, INSERM/CNRS/UPS, Toulouse, France.
2
Université Paul Sabatier Toulouse 3, Toulouse, France.
3
CPTP, U1043, INSERM/CNRS/UPS, Toulouse, France. bahraoui@cict.fr.
4
Université Paul Sabatier Toulouse 3, Toulouse, France. bahraoui@cict.fr.

Abstract

HIV-1 Tat protein induces the production of CXCL8 chemokine in a TLR4/MD2 and PKC dependent manner. The objective of this study was to understand whether these two pathways were distinct or constituted a single common pathway, and to determine the nature of the PKC isoforms involved and their interrelation with the activation of NF-κB and CXCL8 gene product expression. Here, we show that Tat-induced CXCL8 production is essentially dependent on the activation of PKC delta isoform, as shown a) by the capacity of PKC delta dominant negative (DN), and Rottlerin, a selective PKC delta pharmacological inhibitor, to inhibit Tat-induced CXCL8 production and b) by the ability of the constitutively active (CAT) isoform of PKC delta to induce CXCL8 production in a HEK cell line in the absence of Tat stimulation. The finding that comparable amounts of CXCL8 were produced following stimulation with either Tat protein, PKC-delta CAT transfection, or both, argue for the implication of one common pathway where PKC delta is activated downstream of TLR4 recruitment and leads to the activation of NF-κB. Altogether, our results underline the crucial role of PKC delta isoform in activating gene expression of CXCL8, a cytokine largely implicated in the physiopathology of HIV-1 infection.

PMID:
28539656
PMCID:
PMC5443767
DOI:
10.1038/s41598-017-02468-8
[Indexed for MEDLINE]
Free PMC Article

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