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DNAJA4 deficiency enhances NF-kappa B-related growth arrest induced by hyperthermia in human keratinocytes.

Authors :
Sun YZ
Ren Y
Zhang YJ
Han Y
Yang Y
Gao YL
Zhu LL
Qi RQ
Chen HD
Gao XH
Source :
Journal of dermatological science [J Dermatol Sci] 2018 Sep; Vol. 91 (3), pp. 256-267. Date of Electronic Publication: 2018 May 23.
Publication Year :
2018

Abstract

Background: Hyperthermia is an effective treatment against cancer and human papillomavirus (HPV) infection. Previous studies have shown that heat shock proteins are crucial to the action of hyperthermia.<br />Objectives: To examine the effects of hyperthermia in combination with DNAJA4-deficiency on human keratinocytes and Condyloma acumunatum (CA) tissues.<br />Methods: HaCaT cells were subjected to 44°C (compared to 37°C) waterbath for 30min for stimulation. Foreskin or CA tissues obtained from patients undergoing circumcision or pathological examination were bisected and subjected to similar treatments. DNAJA4-knockout (KO) HaCaT cells were generated with CRISPR/Cas9 technology. mRNA and protein expressions were determined using rt-qPCR and western-blotting. Cell cycle distribution, apoptosis and senescence were analyzed by flow cytometry.<br />Results: DNAJA4 was induced in HaCaT cells, foreskin and CA tissues subjected to hyperthermia at both transcriptional and translational levels. NF-kB, <superscript>3</superscript> was activated by hyperthermia in HaCaT cells, and further enhanced by DNAJA4-deficiency. Transcription of TNF-α <superscript>4</superscript> ; IL-1B, <superscript>5</superscript> TNFAIP3 <superscript>6</superscript> and IL-8 <superscript>7</superscript> were induced in HaCaT cells subjected to hyperthermia. DNAJA4-knockout promoted transcriptions of TNF-α and IL-1B, whereas decreased that of TNFAIP3 and IL-8. Reduced cell survival, proliferation and viability were demonstrated using flow cytometry and MTS assays. Furthermore, NF-kB inhibitors reversed most of the phenotypes observed.<br />Conclusions: Hyperthermia reduced HaCaT cell proliferation and promoted cytokine expressions responsible for anti-viral activity, mainly through a NF-kB dependent pathway. DNAJA4-deficiency enhanced the activation of NF-kB by hyperthermia in HaCaT cells, indicating that DNAJA4 may be a promising therapeutic target for use in the treatment of cutaneous HPV infections.<br /> (Copyright © 2018 Japanese Society for Investigative Dermatology. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-569X
Volume :
91
Issue :
3
Database :
MEDLINE
Journal :
Journal of dermatological science
Publication Type :
Academic Journal
Accession number :
29807809
Full Text :
https://doi.org/10.1016/j.jdermsci.2018.05.006