Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway

This study aimed to investigate the effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 signaling pathway. A total of 43 adult female Wistar rats were selected and injected with HeLa cells in the caudal vein to construct a r...

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Main Authors: Song-An Zhang, Hu-Er-Xi-Dan Niyazi, Wen Hong, Gu-Li-Xian Tuluwengjiang, Lei Zhang, Yang Zhang, Wei-Peng Su, Yong-Xing Bao
Format: Article
Language:English
Published: IOS Press 2017-03-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317692237
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spelling doaj-6d42cd2b4ab548778670b7673505f6d02021-05-02T15:00:00ZengIOS PressTumor Biology1423-03802017-03-013910.1177/1010428317692237Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathwaySong-An Zhang0Hu-Er-Xi-Dan Niyazi1Wen Hong2Gu-Li-Xian Tuluwengjiang3Lei Zhang4Yang Zhang5Wei-Peng Su6Yong-Xing Bao7Cancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaCancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaAnus-Intestines Department, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaXinjiang Medical University, Urumqi, P.R. ChinaCancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaCancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaCancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaCancer Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. ChinaThis study aimed to investigate the effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 signaling pathway. A total of 43 adult female Wistar rats were selected and injected with HeLa cells in the caudal vein to construct a rat model of cervical cancer. All model rats were randomly divided into the radiotherapy group ( n  = 31) and the control group ( n  = 12). The immunophenotype of Treg cells was detected by the flow cytometry. The protein expressions of EBI3, PD-1, and PD-L1 in cervical cancer tissues were tested by the streptavidin–peroxidase method. HeLa cells in the logarithmic growth phase were divided into four groups: the blank, the negative control group, the EBI3 mimics group, and the EBI3 inhibitors group. Western blotting was used to detect PD-1 and PD-L1 protein expressions. MTT assay was performed to measure the proliferation of Treg cells. Flow cytometry was used to detect cell cycle and apoptosis, and CD4 + /CD8 + T cell ratio in each group. Compared with before and 1 week after radiotherapy, the percentages of CD4 + T cells and CD8 + T cells were significantly decreased in the radiotherapy group at 1 month after radiotherapy. Furthermore, down-regulation of EBI3 and up-regulation of PD-1 and PD-L1 were observed in cervical cancer tissues at 1 month after radiotherapy. In comparison to the blank and negative control groups, increased expression of EBI3 and decreased expressions of PD-1 and PD-L1 were found in the EBI3 mimics group. However, the EBI3 inhibitors group had a lower expression of EBI3 and higher expressions of PD-1 and PD-L1 than those in the blank and negative control groups. The EBI3 mimics group showed an increase in the optical density value (0.43 ± 0.05), while a decrease in the optical density value (0.31 ± 0.02) was found in the EBI3 inhibitors group. Moreover, compared with the blank and negative control groups, the apoptosis rates of Treg/CD4 + T/CD8 + T cells were decreased in the EBI3 mimics group, but the EBI3 inhibitors group exhibited an increase in apoptosis rate. In conclusion, over-expression of EBI3 could reduce the apoptosis of Treg/CD4 + T/CD8 + T cells and prevent radiation-induced immunosuppression of cervical cancer HeLa cells by inhibiting the activation of PD-1/PD-L1 signaling pathway.https://doi.org/10.1177/1010428317692237
collection DOAJ
language English
format Article
sources DOAJ
author Song-An Zhang
Hu-Er-Xi-Dan Niyazi
Wen Hong
Gu-Li-Xian Tuluwengjiang
Lei Zhang
Yang Zhang
Wei-Peng Su
Yong-Xing Bao
spellingShingle Song-An Zhang
Hu-Er-Xi-Dan Niyazi
Wen Hong
Gu-Li-Xian Tuluwengjiang
Lei Zhang
Yang Zhang
Wei-Peng Su
Yong-Xing Bao
Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
Tumor Biology
author_facet Song-An Zhang
Hu-Er-Xi-Dan Niyazi
Wen Hong
Gu-Li-Xian Tuluwengjiang
Lei Zhang
Yang Zhang
Wei-Peng Su
Yong-Xing Bao
author_sort Song-An Zhang
title Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
title_short Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
title_full Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
title_fullStr Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
title_full_unstemmed Effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 pathway
title_sort effect of ebi3 on radiation-induced immunosuppression of cervical cancer hela cells by regulating treg cells through pd-1/pd-l1 pathway
publisher IOS Press
series Tumor Biology
issn 1423-0380
publishDate 2017-03-01
description This study aimed to investigate the effect of EBI3 on radiation-induced immunosuppression of cervical cancer HeLa cells by regulating Treg cells through PD-1/PD-L1 signaling pathway. A total of 43 adult female Wistar rats were selected and injected with HeLa cells in the caudal vein to construct a rat model of cervical cancer. All model rats were randomly divided into the radiotherapy group ( n  = 31) and the control group ( n  = 12). The immunophenotype of Treg cells was detected by the flow cytometry. The protein expressions of EBI3, PD-1, and PD-L1 in cervical cancer tissues were tested by the streptavidin–peroxidase method. HeLa cells in the logarithmic growth phase were divided into four groups: the blank, the negative control group, the EBI3 mimics group, and the EBI3 inhibitors group. Western blotting was used to detect PD-1 and PD-L1 protein expressions. MTT assay was performed to measure the proliferation of Treg cells. Flow cytometry was used to detect cell cycle and apoptosis, and CD4 + /CD8 + T cell ratio in each group. Compared with before and 1 week after radiotherapy, the percentages of CD4 + T cells and CD8 + T cells were significantly decreased in the radiotherapy group at 1 month after radiotherapy. Furthermore, down-regulation of EBI3 and up-regulation of PD-1 and PD-L1 were observed in cervical cancer tissues at 1 month after radiotherapy. In comparison to the blank and negative control groups, increased expression of EBI3 and decreased expressions of PD-1 and PD-L1 were found in the EBI3 mimics group. However, the EBI3 inhibitors group had a lower expression of EBI3 and higher expressions of PD-1 and PD-L1 than those in the blank and negative control groups. The EBI3 mimics group showed an increase in the optical density value (0.43 ± 0.05), while a decrease in the optical density value (0.31 ± 0.02) was found in the EBI3 inhibitors group. Moreover, compared with the blank and negative control groups, the apoptosis rates of Treg/CD4 + T/CD8 + T cells were decreased in the EBI3 mimics group, but the EBI3 inhibitors group exhibited an increase in apoptosis rate. In conclusion, over-expression of EBI3 could reduce the apoptosis of Treg/CD4 + T/CD8 + T cells and prevent radiation-induced immunosuppression of cervical cancer HeLa cells by inhibiting the activation of PD-1/PD-L1 signaling pathway.
url https://doi.org/10.1177/1010428317692237
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