Expression of testis specific expressed gene 1 in ethanol-induced mouse testis injury model and significance
Chaohui Gu, Fengyan Tian, Guanru Li, Zhankui Jia, Zhenglei Meng, Ke Sun, Jinxing Wei
Abstract
Chaohui Gu, Fengyan Tian, Guanru Li, Zhankui Jia, Zhenglei Meng, Ke Sun, Jinxing Wei
Abstract
Objective To explore the cellular localization and transcript levels of testis specific expressed gene 1 (TSEG-1) in ethanol-induced mouse testis injury model.Methods Twelve male Kunming mice were divided into normal saline solution group (n =6) and ethanol injection group (n =6).The morphological changes of testes were observed by hematoxylin and eosin (HE) staining.The transcriptional and protein levels of TSEG-1 were detected by real-time reverse transcriptase-polymerase chain reaction (RT-qPCR),Immunohistochemistry (IHC) and Western blotting.Results Intraperitoneal injection of 3 g ethanol (15%,V/V)/kg body weight for 14 days induced mouse testis injury.As compared with normal saline solution group,85.6% serminous tubules disappeared,the number of Ⅰ-Ⅳ-stage spermatogenic cells was reduced,and 78.2% spermatocytes and spermatids had nuclei shrinkage in ethanol injection group.Extensive TSEG-1 mRNA levels were observed in control testes,mainly localizing in spermatocytes and early spermatids.The transcripts of TSEG-1 (7.500 ± 0.657,n =6) were up-regulated to 8 folds in ethanol injection group as compared with those in normal saline solution control group (0.985 ±0.231,n =6),with the difference being significant (t =22.915,P < 0.01).Especially,the protein expression of TSEG-1 (1.360 ±0.202,n =6) was up-regulated to 4 folds in ethanol injection group as compared with that in normal saline solution control group (0.330 ±0.112,n =6),with the difference being significant,t =10.69,P < 0.01.Conclusion Ethanol-induced testis injury model was successfully constructed by intraperitoneal injection of ethanol.The novel gene TSEG-1 may play a role in the pathogenesis of ethanol-induced testis injury model,which laid the basis for further study on its function in testis diseases. Key words: Ethanol; Testis injury; Testis specific expressed gene 1
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Objective To explore the cellular localization and transcript levels of testis specific expressed gene 1 (TSEG-1) in ethanol-induced mouse testis injury model.Methods Twelve male Kunming mice were divided into normal saline solution group (n =6) and ethanol injection group (n =6).The morphological changes of testes were observed by hematoxylin and eosin (HE) staining.The transcriptional and protein levels of TSEG-1 were detected by real-time reverse transcriptase-polymerase chain reaction (RT-qPCR),Immunohistochemistry (IHC) and Western blotting.Results Intraperitoneal injection of 3 g ethanol (15%,V/V)/kg body weight for 14 days induced mouse testis injury.As compared with normal saline solution group,85.6% serminous tubules disappeared,the number of Ⅰ-Ⅳ-stage spermatogenic cells was reduced,and 78.2% spermatocytes and spermatids had nuclei shrinkage in ethanol injection group.Extensive TSEG-1 mRNA levels were observed in control testes,mainly localizing in spermatocytes and early spermatids.The transcripts of TSEG-1 (7.500 ± 0.657,n =6) were up-regulated to 8 folds in ethanol injection group as compared with those in normal saline solution control group (0.985 ±0.231,n =6),with the difference being significant (t =22.915,P < 0.01).Especially,the protein expression of TSEG-1 (1.360 ±0.202,n =6) was up-regulated to 4 folds in ethanol injection group as compared with that in normal saline solution control group (0.330 ±0.112,n =6),with the difference being significant,t =10.69,P < 0.01.Conclusion Ethanol-induced testis injury model was successfully constructed by intraperitoneal injection of ethanol.The novel gene TSEG-1 may play a role in the pathogenesis of ethanol-induced testis injury model,which laid the basis for further study on its function in testis diseases. Key words: Ethanol; Testis injury; Testis specific expressed gene 1
Key concepts: Saline, Ethanol, Intraperitoneal injection, H&E stain, Immunohistochemistry, Andrology, Messenger RNA, Internal medicine