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下调 PHGDH 影响精索静脉曲张中支持细胞的乳酸生成。

Down regulating PHGDH affects the lactate production of sertoli cells in varicocele.

机构信息

Department of Urology, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

出版信息

Reprod Biol Endocrinol. 2020 Jul 14;18(1):70. doi: 10.1186/s12958-020-00625-9.

Abstract

BACKGROUND

Although varicocele is considered to be one of the leading causes of male infertility, the precise mechanism underlying how varicocele leads to male infertility is not completely understood. We found the lactate concentration on the varicocele side of the patients was decreased compare with peripheral venous blood. In the testicles, the lactate produced by the sertoli cells through the glycolysis pathway provides most of the energy needed for spermatogenesis, the reduction of lactate will affect spermatogenesis. The objective of this study was to investigate the mechanism of this abnormal energy metabolism phenomenon in varicocele.

METHODS

In this study, we collected the testicular tissue from patients with varicocele, the glycolysis related proteins PHGDH was identified by iTRAQ proteomics technology. Experimental rat varicocele model was constructed according to our new clip technique, the mRNA and protein expression levels of PHGDH were examined with qRT-PCR and Western blotting. We constructed a sertoli cell of PHGDH down-regulation model, and then detected the glucose consumption, LDH activities and lactate production in the sertoli cells. Western blot was conducted to investigate the effects of PHGDH on the expression of phosphoserine phosphatase (PSPH) and Pyruvate kinase M2 (PKM2). Flow cytometry was used to detect the cell apoptosis and cell cycle in sertoli cells.

RESULTS

The results showed that testicular protein PHGDH was down-regulated in patients with varicocele and in experimental rat varicocele model. Down-regulation of PHGDH in sertoli cells significantly decreased the glucose consumption, LDH activities and lactate production in the sertoli cells, indicating that the low expression of PHGDH ultimately led to a decrease in lactate production by affecting the glycolysis. The Western blot results showed that the down-regulation of PHGDH significantly reduced the expression of pathway protein PSPH and PKM2, leading to the reduction of lactate production. Moreover, PHGDH knockdown can promote apoptosis and inhibit cell cycle to affect cell growth.

CONCLUSIONS

Overall, we conformed that varicocele lead to the decreasing of testis lactate production. Down-regulation of PHGDH in sertoli cells may mediate the process of abnormal glucose metabolism. Our study provide new insight into the mechanisms underlying metabolism-associated male infertility and suggests a novel therapeutic target for male infertility.

摘要

背景

尽管精索静脉曲张被认为是男性不育的主要原因之一,但精索静脉曲张导致男性不育的确切机制尚不完全清楚。我们发现患者精索静脉曲张侧的乳酸浓度较外周静脉血降低。在睾丸中,支持细胞通过糖酵解途径产生的乳酸为精子发生提供了大部分所需的能量,乳酸的减少会影响精子发生。本研究的目的是探讨精索静脉曲张中这种异常能量代谢现象的机制。

方法

本研究收集精索静脉曲张患者的睾丸组织,应用 iTRAQ 蛋白质组学技术鉴定糖酵解相关蛋白 PHGDH。根据我们新的夹闭技术构建实验性大鼠精索静脉曲张模型,采用 qRT-PCR 和 Western blot 检测 PHGDH 的 mRNA 和蛋白表达水平。构建 PHGDH 下调的支持细胞模型,然后检测支持细胞的葡萄糖消耗、LDH 活性和乳酸产生。Western blot 检测 PHGDH 对磷酸丝氨酸磷酸酶(PSPH)和丙酮酸激酶 M2(PKM2)表达的影响。流式细胞术检测支持细胞的细胞凋亡和细胞周期。

结果

结果显示,精索静脉曲张患者和实验性大鼠精索静脉曲张模型睾丸组织蛋白 PHGDH 下调。支持细胞中 PHGDH 的下调显著降低了支持细胞的葡萄糖消耗、LDH 活性和乳酸产生,表明低表达 PHGDH 通过影响糖酵解最终导致乳酸产生减少。Western blot 结果表明,PHGDH 下调显著降低了通路蛋白 PSPH 和 PKM2 的表达,导致乳酸产生减少。此外,PHGDH 敲低可促进细胞凋亡并抑制细胞周期,从而影响细胞生长。

结论

总之,我们证实精索静脉曲张导致睾丸乳酸产生减少。支持细胞中 PHGDH 的下调可能介导了异常葡萄糖代谢的过程。我们的研究为代谢相关男性不育的机制提供了新的见解,并为男性不育症提供了新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8219/7359552/e3e66390e698/12958_2020_625_Fig1_HTML.jpg

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