Huang I-Shen, Li Li-Hua, Chen Wei-Jen, Huang Eric Yi-Hsiu, Juan Chi-Chang, Huang William J
Department of Urology, Taipei Veterans General Hospital, Taipei, Taiwan.
Department of Physiology, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Eur Urol Open Sci. 2023 Jul 7;54:88-96. doi: 10.1016/j.euros.2023.06.004. eCollection 2023 Aug.
The primary microenvironment of the testis comprises testicular interstitial fluid (TIF) surrounding the seminiferous tubules and testicular interstitial tissue. The pathological alterations of germ and Sertoli cells could affect the TIF composition and might contain putative biomarkers for monitoring active spermatogenesis.
We identified differentially expressed proteins in the TIF of patients with obstructive (OA) or nonobstructive (NOA) azoospermia to elucidate the underlying etiology of defective spermatogenesis.
We prospectively enrolled nine patients, including three men with OA and six with NOA with ( = 3) and without ( = 3) successful sperm retrieval. Their TIF was collected during the testicular sperm extraction procedure.
TIF was analyzed using liquid chromatography-tandem mass spectrometry to identify differentially expressed proteins specific to OA and NOA with or without successful sperm retrieval. The dysregulated protein was further validated using Western blotting.
Among the 555 TIF proteins identified in NOA patients, 14 were downregulated relative to OA patients. These proteins participate in biological processes such as proteolysis, complement activation, and immune responses; complement and coagulation cascade pathways were also enriched. Furthermore, 68 proteins with significantly higher levels were identified in the TIF of NOA patients with successful sperm retrieval than in those with failed sperm retrieval; these are mainly implicated in oxidation-reduction processes. The expression of calreticulin, which can distinguish successful and failed testicular sperm retrieval in the NOA group, was validated by Western blotting.
We provide the first scientific evaluation of TIF protein composition in men with azoospermia. These findings will help identify the physiological and pathological roles of each protein in regulating sperm production. Thus, our study underscores the potential of TIF in sperm retrieval biomarker discovery and would serve as a foundation for further studies to improve treatment strategies against azoospermia.
Using a proteomic approach, we identified and analyzed the total protein content of testicular interstitial fluid in humans with defective spermatogenesis for the first time and discovered altered protein expression patterns in patients with nonobstructive azoospermia (NOA). Proteins related to oxidation-reduction processes were upregulated in NOA patients with successful sperm retrieval compared with those with failed sperm retrieval. This can aid the development of novel diagnostic tools for successful testicular sperm retrieval.
睾丸的主要微环境包括围绕生精小管的睾丸间质液(TIF)和睾丸间质组织。生殖细胞和支持细胞的病理改变可能会影响TIF的组成,并且可能包含用于监测活跃精子发生的潜在生物标志物。
我们鉴定了梗阻性(OA)或非梗阻性(NOA)无精子症患者TIF中差异表达的蛋白质,以阐明精子发生缺陷的潜在病因。
设计、场所和参与者:我们前瞻性招募了9名患者,包括3名OA患者和6名NOA患者,其中3名成功获取精子,3名未成功获取精子。在睾丸精子提取过程中收集他们的TIF。
使用液相色谱-串联质谱法分析TIF,以鉴定OA和NOA患者中特定的差异表达蛋白质,无论是否成功获取精子。使用蛋白质印迹法进一步验证失调的蛋白质。
在NOA患者中鉴定出的555种TIF蛋白质中,相对于OA患者,有14种蛋白质表达下调。这些蛋白质参与蛋白水解、补体激活和免疫反应等生物学过程;补体和凝血级联途径也得到了富集。此外,与未成功获取精子的NOA患者相比,成功获取精子的NOA患者的TIF中鉴定出68种水平显著更高的蛋白质;这些蛋白质主要参与氧化还原过程。通过蛋白质印迹法验证了钙网蛋白的表达,该蛋白可区分NOA组中睾丸精子获取的成功与失败。
我们首次对无精子症男性的TIF蛋白质组成进行了科学评估。这些发现将有助于确定每种蛋白质在调节精子产生中的生理和病理作用。因此,我们的研究强调了TIF在发现精子获取生物标志物方面的潜力,并将为进一步研究改善无精子症治疗策略奠定基础。
我们首次使用蛋白质组学方法鉴定并分析了精子发生缺陷的人类睾丸间质液中的总蛋白质含量,并发现非梗阻性无精子症(NOA)患者的蛋白质表达模式发生了改变。与未成功获取精子的NOA患者相比,成功获取精子的NOA患者中与氧化还原过程相关的蛋白质上调。这有助于开发用于成功获取睾丸精子的新型诊断工具。