Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association

Interleukin (IL)-32θ, a newly identified IL-32 isoform, has been reported to exert pro-inflammatory effects through the association with protein kinase C delta (PKCδ). In this study, we further examined the effects of IL-32θ on IL-13 and IL-13Rα2 expression and th...

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Main Authors: Thu-Huyen Pham, Yesol Bak, Jae-Wook Oh, Jingi Hong, Seungyeoun Lee, Jin Tae Hong, Do-Young Yoon
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/8/1949
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spelling doaj-3d279902df394f7691671cd096ab77172020-11-24T21:49:08ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-04-01208194910.3390/ijms20081949ijms20081949Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 AssociationThu-Huyen Pham0Yesol Bak1Jae-Wook Oh2Jingi Hong3Seungyeoun Lee4Jin Tae Hong5Do-Young Yoon6Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, KoreaDepartment of Bioscience and Biotechnology, Konkuk University, Seoul 05029, KoreaDepartment of Stem cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, KoreaDepartment of Mathematics and Statistics, Sejong University, Seoul 05006, KoreaDepartment of Mathematics and Statistics, Sejong University, Seoul 05006, KoreaCollege of Pharmacy and Medical Research Center, Chungbuk National University, Chungbuk 28160, KoreaDepartment of Bioscience and Biotechnology, Konkuk University, Seoul 05029, KoreaInterleukin (IL)-32θ, a newly identified IL-32 isoform, has been reported to exert pro-inflammatory effects through the association with protein kinase C delta (PKCδ). In this study, we further examined the effects of IL-32θ on IL-13 and IL-13Rα2 expression and the related mechanism in THP-1 cells. Upon stimulating IL-32θ-expressing and non-expressing cells with phorbol 12-myristate 13-acetate (PMA), the previous microarray analysis showed that IL-13Rα2 and IL-13 mRNA expression were significantly decreased by IL-32θ. The protein expression of these factors was also confirmed to be down-regulated. The nuclear translocation of transcription factors STAT3 and STAT6, which are necessary for IL-13Rα2 and IL-13 promoter activities, was suppressed by IL-32θ. Additionally, a direct association was found between IL-32θ, PKCδ, and signal transducer and activator of transcription 3 (STAT3), but not STAT6, revealing that IL-32θ might act mainly through STAT3 and indirectly affect STAT6. Moreover, the interaction of IL-32θ with STAT3 requires PKCδ, since blocking PKCδ activity eliminated the interaction and consequently limited the inhibitory effect of IL-32θ on STAT3 activity. Interfering with STAT3 or STAT6 binding by decoy oligodeoxynucleotides (ODNs) identified that IL-32θ had additive effects with the STAT3 decoy ODN to suppress IL-13 and IL-13Rα2 mRNA expression. Taken together, our data demonstrate the intracellular interaction of IL-32θ, PKCδ, and STAT3 to regulate IL-13 and IL-13Rα2 synthesis, supporting the role of IL-32θ as an inflammatory modulator.https://www.mdpi.com/1422-0067/20/8/1949IL-13Rα2IL-13 signalingIL-32θSTAT3 activationPKCδ
collection DOAJ
language English
format Article
sources DOAJ
author Thu-Huyen Pham
Yesol Bak
Jae-Wook Oh
Jingi Hong
Seungyeoun Lee
Jin Tae Hong
Do-Young Yoon
spellingShingle Thu-Huyen Pham
Yesol Bak
Jae-Wook Oh
Jingi Hong
Seungyeoun Lee
Jin Tae Hong
Do-Young Yoon
Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
International Journal of Molecular Sciences
IL-13Rα2
IL-13 signaling
IL-32θ
STAT3 activation
PKCδ
author_facet Thu-Huyen Pham
Yesol Bak
Jae-Wook Oh
Jingi Hong
Seungyeoun Lee
Jin Tae Hong
Do-Young Yoon
author_sort Thu-Huyen Pham
title Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
title_short Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
title_full Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
title_fullStr Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
title_full_unstemmed Inhibition of IL-13 and IL-13Rα2 Expression by IL-32θ in Human Monocytic Cells Requires PKCδ and STAT3 Association
title_sort inhibition of il-13 and il-13rα2 expression by il-32θ in human monocytic cells requires pkcδ and stat3 association
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-04-01
description Interleukin (IL)-32θ, a newly identified IL-32 isoform, has been reported to exert pro-inflammatory effects through the association with protein kinase C delta (PKCδ). In this study, we further examined the effects of IL-32θ on IL-13 and IL-13Rα2 expression and the related mechanism in THP-1 cells. Upon stimulating IL-32θ-expressing and non-expressing cells with phorbol 12-myristate 13-acetate (PMA), the previous microarray analysis showed that IL-13Rα2 and IL-13 mRNA expression were significantly decreased by IL-32θ. The protein expression of these factors was also confirmed to be down-regulated. The nuclear translocation of transcription factors STAT3 and STAT6, which are necessary for IL-13Rα2 and IL-13 promoter activities, was suppressed by IL-32θ. Additionally, a direct association was found between IL-32θ, PKCδ, and signal transducer and activator of transcription 3 (STAT3), but not STAT6, revealing that IL-32θ might act mainly through STAT3 and indirectly affect STAT6. Moreover, the interaction of IL-32θ with STAT3 requires PKCδ, since blocking PKCδ activity eliminated the interaction and consequently limited the inhibitory effect of IL-32θ on STAT3 activity. Interfering with STAT3 or STAT6 binding by decoy oligodeoxynucleotides (ODNs) identified that IL-32θ had additive effects with the STAT3 decoy ODN to suppress IL-13 and IL-13Rα2 mRNA expression. Taken together, our data demonstrate the intracellular interaction of IL-32θ, PKCδ, and STAT3 to regulate IL-13 and IL-13Rα2 synthesis, supporting the role of IL-32θ as an inflammatory modulator.
topic IL-13Rα2
IL-13 signaling
IL-32θ
STAT3 activation
PKCδ
url https://www.mdpi.com/1422-0067/20/8/1949
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