Palladino Michael A, Fasano Genevieve A, Patel Dharm, Dugan Christine, London Marie
Monmouth University, 400 Cedar Avenue, West Long Branch, NJ 07764 USA.
Basic Clin Androl. 2018 Nov 16;28:14. doi: 10.1186/s12610-018-0079-x. eCollection 2018.
Bacterial infection and inflammation of the testis impairs fertility, yet an understanding of inflammatory responses of the testis is incomplete. We are interested in identifying gene pathways involved in the detection and clearance of infectious microbes in the male reproductive tract. In previous studies in our lab focused on hypoxia-responsive genes of the testis, preliminary experiments suggested that genes classically categorized as hypoxia genes are also activated during antimicrobial responses. The purpose of this study was to identify hypoxia and inflammatory gene pathways that contribute to antimicrobial protection of the testis and to consider possible cross-talk and interactions between these pathways. Inflammation was induced in Sprague-Dawley rats using or lipopolysaccharide (LPS). Levels of hypoxia-inducible factor-1 (HIF-1α) protein and nuclear factor kappa B (NF-κB) were measured, and hypoxia and inflammatory gene expression patterns in testis were analyzed by gene expression profiling using real-time quantitative PCR arrays.
In LPS-treated rats, HIF-1α protein increased with no change in mRNA. Western Blot analysis also demonstrated no change in NF-κB and inhibitory NFKB alpha (IκBα) protein levels following LPS treatment. Five hypoxia pathway genes ( and , and 11 inflammatory pathway genes ( up-regulated after 3 h of inflammation. and remained elevated at 6 h. Six genes were up-regulated at 6 h only (, . One gene () was down-regulated after 3 h and no genes at 6 h. Electrophoretic mobility shift assay results suggest a decrease in NF-κB binding activity following LPS treatment.
Testicular HIF-1α is up-regulated following LPS-induced inflammation. In contrast to other tissues, in which HIF-1α is up-regulated through transcriptional activation via NF-κB, we conclude that HIF-1α in the testis is not up-regulated through an increase in mRNA or through NF-κB-dependent mechanisms. Hypoxia pathway genes and genes involved in Toll-like receptor (TLR) and cytokine-mediated signaling comprise major functional categories of up-regulated genes, demonstrating that both hypoxia and classic inflammatory pathways are involved in inflammatory responses of the testis.
睾丸的细菌感染和炎症会损害生育能力,但对睾丸炎症反应的了解并不完整。我们感兴趣的是确定参与男性生殖道中感染性微生物检测和清除的基因通路。在我们实验室之前关于睾丸缺氧反应基因的研究中,初步实验表明,经典分类为缺氧基因的基因在抗菌反应期间也会被激活。本研究的目的是确定有助于睾丸抗菌保护的缺氧和炎症基因通路,并考虑这些通路之间可能的相互作用和对话。使用或脂多糖(LPS)在斯普拉格-道利大鼠中诱导炎症。测量缺氧诱导因子-1(HIF-1α)蛋白和核因子κB(NF-κB)的水平,并使用实时定量PCR阵列通过基因表达谱分析睾丸中的缺氧和炎症基因表达模式。
在LPS处理的大鼠中,HIF-1α蛋白增加,而mRNA无变化。蛋白质印迹分析还表明,LPS处理后NF-κB和抑制性NFKBα(IκBα)蛋白水平没有变化。五个缺氧通路基因(和,以及11个炎症通路基因(在炎症3小时后上调。和在6小时时仍保持升高。六个基因仅在6小时时上调(,。一个基因()在3小时后下调,在6小时时无基因下调。电泳迁移率变动分析结果表明,LPS处理后NF-κB结合活性降低。
LPS诱导的炎症后,睾丸中的HIF-1α上调。与其他组织不同,在其他组织中HIF-1α通过NF-κB的转录激活而上调,我们得出结论,睾丸中的HIF-1α不是通过mRNA增加或通过NF-κB依赖性机制上调的。缺氧通路基因以及参与Toll样受体(TLR)和细胞因子介导信号传导的基因构成上调基因的主要功能类别,表明缺氧和经典炎症通路均参与睾丸的炎症反应。