Carcinogenesis, Teratogenesis & Mutagenesis ›› 2020, Vol. 32 ›› Issue (5): 329-335.doi: 10.3969/j.issn.1004-616x.2020.05.001

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Effects of SOX30 gene knockout on testicular tissue structure and hormone secretion in male mice

WANG Ping1,2, JIANG Xiao1, HAN Fei1, CUI Zhihong3, TANG Ying1,4, ZHOU Yangxi1,3, LIU Wenbin1, CAO Jia1, LIU Jinyi1   

  1. 1. Institute of Toxicology, College of Preventive Medicine, Army Medical University, Chongqing 400038;
    2. Medical Center of Hematology, The Xinqiao Hospital of Army Medical University, Chongqing 400037;
    3. College of Pharmaceutical Sciences and Chinese Medicine, Southwest University, Chongqing 400715;
    4. Department of Occupational Health and Environmental Hygiene, School of Public Health and Management, Ningxia Medical University, Yinchuan 750004, Ningxia, China
  • Received:2020-07-22 Revised:2020-08-22 Online:2020-10-01 Published:2020-10-12

Abstract: OBJECTIVE: To evaluate the effects of SOX30 gene knockout on testicular tissue structure and hormone secretion in male mice,and to explore the role of SOX30 gene in male reproductive system. METHODS: The SOX30 gene knockout mouse model was constructed by the gene recombination method and genotypes were identified by the PCR method. The male mice were divided into wild type (WW),heterozygous (KW) and homozygous (KK) groups according to the results from genotype identification (2.5 months old). Testicular volume and testicular organ index were calculated. After H&E staining,structures of the testes and epididymes of each mouse were determined,and diameters of the Seminiferous tubule were measured. Levels of the testosteron (T) and inhibin B (INH-B) hormones in homogenates of testicular tissues were detected by ELISA. Expressions of SOX9 and 3β-HSD in testicular tissues were determined by using the immunofluorescence technique. RESULTS: Compared with the WW and KW types,the testicular organ index of KK mice was significantly decreased (P < 0.05). There were no pathological changes in the testes and epididymes of KW and WW mice. On the contrary,testes in KK mice had disordered spermatogenic cells,giant cells,vacuolar degeneration and interstitial hyperplasia. No matured sperm was found in the epididymis of KK mice. The lumen diameters of seminiferous tubules in the KK mice were reduced compared with the WW mice (P < 0.05). In addition,the T and INH-B levels in homogenates from testicular tissues were reduced significantly in the KK compared with the WW and KW mice (P < 0.05). There was no significant difference in the number of Sertoli cells expressing SOX9 between WW and KK mice,but the number of leydig cells expressing 3β-HSD in KK mice was significantly more than that in WW mice (P < 0.05). CONCLUSION: Our results suggest that the knockout of SOX30 induced pathological damage in testes of mice via inhibiting the synthesis of T and INH-B which played important roles in maintaining normal functions of testes.

Key words: SOX30 gene, gene knockout, male, mice, reproduction

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