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Transmembrane BAX Inhibitor Motif-6 (TMBIM6) protects against cisplatin-induced testicular toxicity

Title
Transmembrane BAX Inhibitor Motif-6 (TMBIM6) protects against cisplatin-induced testicular toxicity
Authors
Kim, H.-K.Yadav, R.K.Bhattarai, K.R.Jung, H.-W.Kim, Hyung RyongChae, H.-J.
DGIST Authors
Kim, Hyung Ryong
Issue Date
2018-03
Citation
Human Reproduction, 33(3), 378-389
Type
Article
Article Type
Article
Keywords
cholesterol monooxygenase (side chain cleaving)cisplatinheme oxygenase 1initiation factor 2alphalentivirus vectorpregnenoloneprotein Baxprotein disulfide isomeraseprotein kinase Breactive oxygen metabolitesteroidogenic acute regulatory proteintestosteronetranscription factor Nrf2transmembrane BAX inhibitor motif 6unclassified druganimal cellanimal experimentanimal modelanimal tissueArticlebioaccumulationblood samplingcancer therapycarbonylationcomparative studycontrolled studydrug mechanismendoplasmic reticulumendoplasmic reticulum stressenzyme activitygene overexpressiongene productgene transferimmunoblottingin vitro studyLeydig cellmousenonhumanoxidative stressphenotypic variationpolymerase chain reactionprotein expressionprotein processingquantitative analysisreproductive toxicitysingle drug dosesteroidogenesistestis diseasetestis tissuetestis weighttestosterone blood leveltestosterone synthesisupregulation
ISSN
0268-1161
Abstract
STUDY QUESTION Is the Transmembrane BAX Inhibitor Motif-6 (TMBIM6) involved in the molecular mechanism by which cisplatin causes reproductive toxicity? SUMMARY ANSWER TMBIM6 protects against cisplatin-induced testicular toxicity through up-regulation of heme oxygenase-1 (HO-1),-which maintains the levels of steroidogenic enzymes by decreaseing oxidative stress in the endoplasmic reticulum (ER). WHAT IS KNOWN ALREADY Testosterone production is highly suppressed as a main complication of cisplatin (cis-diamminedichloroplatinum) anticancer therapy. STUDY DESIGN, SIZE, DURATION Groups of seven wild type or Tmbim6 KO C57BL/6J mice were given a single i.p., injection of cisplatin (30 mg/kg body wt) and testis and serum were collected 3 days later. Tmbim6-lentivirus-mediated testicular expression-rescued KO mice were analyzed to confirm function was restored. Tmbim6-over expressing TM3 mouse Leydig cells were exposed to cisplatin in vitro. PARTICIPANTS/MATERIALS, SETTING, METHODS After collection of the specimens serum testosterone level and testicular weight and structure were compared between the groups. Quantitative PCR, immunoblot, and assays for ROS, HO-1 activity and protein disulfide isomerase (PDI) carbonylation were performed. MAIN RESULTS AND THE ROLE OF CHANCE Phospho protein kinase B (p-Akt), nuclear factor erythroid 2 (NFE2)-related factor 2 (Nrf2), and its downstream gene product HO-1 and the levels of testosterone synthesis-associated enzymes, including steroidogenic acute regulatory protein (StAR), a rate limiting enzyme for testosterone production, were significantly expressed in the presence of Tmbim6 and maintained after cisplatin treament. Excessive post-translational oxidation of protein disulfide isomerase (PDI), altered folding capacitance and ROS accumulation, and ER stress were also decreased in the presence of Tmbim6. Higher levels of ER stress and protein hypercarbonylation were consistently observed in KO testis, compared with WT testis. In the Tmbim6 KO mice, lentivirus-mediated testicular expression of Tmbim6 rescued the above phenotypes. Furthermore, the protective role of Tmbim6 against testicular toxicity was consistently shown in Tmbim6-overexpressing TM3 Leydig cells (testosterone producing cells). We conclude that TMBIM6 protects against cisplatin-induced testicular toxicity by inducing HO-1 and enhancing ER folding capacitance. LARGE SCALE DATA N/A LIMITATIONS, REASONS FOR CAUTION This study was performed using a short, 3-day cisplatin treatment condition. Therefore, the results need to be cautiously interpreted with regard to cisplatin-associated chronic toxicity. Moreover, to determine the clinical relevance of the role of TMBIM6, further studies in testicular cancer are needed. WIDER IMPLICATIONS OF THE FINDINGS Cisplatin-associated ER stress and redox imbalance might be implicated as toxicity mechanisms associated with anticancer therapy. STUDY FUNDING/COMPETING INTEREST(S) This study was supported by the National Research Foundation of Korea (2015R1A2A1A13001849). The authors have no competing interests to disclose. © The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology.
URI
http://hdl.handle.net/20.500.11750/6159
DOI
10.1093/humrep/dex381
Publisher
Oxford University Press
Files:
There are no files associated with this item.
Collection:
ETC1. Journal Articles


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