ZnSO^sub 4^ rescued vimentin from collapse in DBP-exposed Sertoli cells by attenuating ER stress and apoptosis

Sertoli cells (SCs) provide physical and nutritional support for spermatogenesis. Dibutyl phthalate (DBP) is a plasticizer that has male reproductive toxicity. The collapse of vimentin in DBP-exposed SCs is thought to induce the sloughing of spermatocytes from seminiferous tubules. In this study, we...

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Veröffentlicht in:Toxicology in vitro 2018-04, Vol.48, p.195
Hauptverfasser: Zhang, Xi, Wang, Xiaogang, Liu, Taixiu, Mo, Min, Ao, Lin, Liu, Jinyi, Cao, Jia, Cui, Zhihong
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container_issue
container_start_page 195
container_title Toxicology in vitro
container_volume 48
creator Zhang, Xi
Wang, Xiaogang
Liu, Taixiu
Mo, Min
Ao, Lin
Liu, Jinyi
Cao, Jia
Cui, Zhihong
description Sertoli cells (SCs) provide physical and nutritional support for spermatogenesis. Dibutyl phthalate (DBP) is a plasticizer that has male reproductive toxicity. The collapse of vimentin in DBP-exposed SCs is thought to induce the sloughing of spermatocytes from seminiferous tubules. In this study, we explored methods to rescue vimentin from collapse in DBP-exposed SCs. DBP not only induced the hyperphosphorylation of vimentin but also triggered endoplasmic reticulum (ER) stress and apoptosis in SCs. Treatment with BAPTA-AM, an antagonist of Ca2+, significantly decreased the level of phosphorylated vimentin, while LY294002, an inhibitor of Akt1, did not. ER stress and apoptosis remained at high levels, and the distribution of vimentin was not improved. ZnSO4 treatment did not decrease the level of phosphorylated vimentin. However, after treatment, ER stress and apoptosis were obviously inhibited, and the distribution of vimentin was reconverted. These results indicated that ZnSO4 could alleviate the collapse of vimentin by attenuating ER stress and apoptosis. This study suggested that an appropriate zinc supply might be a choice to alleviate DBP-induced adverse reproductive effects.
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Dibutyl phthalate (DBP) is a plasticizer that has male reproductive toxicity. The collapse of vimentin in DBP-exposed SCs is thought to induce the sloughing of spermatocytes from seminiferous tubules. In this study, we explored methods to rescue vimentin from collapse in DBP-exposed SCs. DBP not only induced the hyperphosphorylation of vimentin but also triggered endoplasmic reticulum (ER) stress and apoptosis in SCs. Treatment with BAPTA-AM, an antagonist of Ca2+, significantly decreased the level of phosphorylated vimentin, while LY294002, an inhibitor of Akt1, did not. ER stress and apoptosis remained at high levels, and the distribution of vimentin was not improved. ZnSO4 treatment did not decrease the level of phosphorylated vimentin. However, after treatment, ER stress and apoptosis were obviously inhibited, and the distribution of vimentin was reconverted. These results indicated that ZnSO4 could alleviate the collapse of vimentin by attenuating ER stress and apoptosis. This study suggested that an appropriate zinc supply might be a choice to alleviate DBP-induced adverse reproductive effects.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><language>eng</language><publisher>Oxford: Elsevier Science Ltd</publisher><subject>AKT1 protein ; Apoptosis ; Calcium ; Calcium ions ; Collapse ; Dibutyl phthalate ; Endoplasmic reticulum ; Exposure ; Phosphorylation ; Sertoli cells ; Spermatocytes ; Spermatogenesis ; Stress ; Stresses ; Toxicity ; Tubules ; Vimentin ; Zinc</subject><ispartof>Toxicology in vitro, 2018-04, Vol.48, p.195</ispartof><rights>Copyright Elsevier Science Ltd. 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Dibutyl phthalate (DBP) is a plasticizer that has male reproductive toxicity. The collapse of vimentin in DBP-exposed SCs is thought to induce the sloughing of spermatocytes from seminiferous tubules. In this study, we explored methods to rescue vimentin from collapse in DBP-exposed SCs. DBP not only induced the hyperphosphorylation of vimentin but also triggered endoplasmic reticulum (ER) stress and apoptosis in SCs. Treatment with BAPTA-AM, an antagonist of Ca2+, significantly decreased the level of phosphorylated vimentin, while LY294002, an inhibitor of Akt1, did not. ER stress and apoptosis remained at high levels, and the distribution of vimentin was not improved. ZnSO4 treatment did not decrease the level of phosphorylated vimentin. However, after treatment, ER stress and apoptosis were obviously inhibited, and the distribution of vimentin was reconverted. These results indicated that ZnSO4 could alleviate the collapse of vimentin by attenuating ER stress and apoptosis. 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subjects AKT1 protein
Apoptosis
Calcium
Calcium ions
Collapse
Dibutyl phthalate
Endoplasmic reticulum
Exposure
Phosphorylation
Sertoli cells
Spermatocytes
Spermatogenesis
Stress
Stresses
Toxicity
Tubules
Vimentin
Zinc
title ZnSO^sub 4^ rescued vimentin from collapse in DBP-exposed Sertoli cells by attenuating ER stress and apoptosis
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