Department of Dermatology, Changzheng Hospital, Naval Medical University, No. 415 Fengyang Road, Shanghai 200003, China.
Department of Dermatology, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Biomed Res Int. 2022 Mar 26;2022:5532118. doi: 10.1155/2022/5532118. eCollection 2022.
Cryptococcosis is an invasive fungal disease that is associated with an increasing prevalence along with a very high fatality and is primarily caused by Cryptococcus. However, its mechanism to cause pathogenicity is not yet completely understood. In this study, we aim to screen the lncRNA markers in human monocytic (THP-1) cells infected by () through high-throughput sequencing technology and to explore its effects on biological functions.
We initially conducted an lncRNA microarray analysis of the THP-1 cells infected by C. neoformans and normal THP-1 cells. Based upon these data, RT-qPCR was used to verify the expressions of the selected lncRNAs and mRNAs. We then performed functional and pathway enrichment analyses. Lastly, target prediction was performed by using the lncRNA target tool which was based on the differentially expressed lncRNAs.
We determined 81 upregulated and 96 downregulated lncRNAs using microarray. In addition, the profiling data showed 42 upregulated and 57 downregulated genes and discovered that neuroactive ligand-receptor interaction, tyrosine metabolism, and phenylalanine metabolism are extremely impaired in the regulation of infection. GO enrichment analysis of the 99 differentially expressed mRNAs exhibited that these modules showed different signaling pathways and biological mechanisms like protein binding and metal ion binding. Moreover, lncRNAs and mRNAs were analyzed for their coexpression relations. A qRT-PCR analysis confirmed that the expression of the top 10 differently expressed mRNA and lincRNA. The expressions of the lncRNAs after infection in THP-1 cells were detected by RNA-sequence, suggesting that microarray analysis could reveal lncRNAs having functional significance that might be linked with the progression of patients.
The current study analyzed the differential lncRNAs and mRNAs in infection and predicted the corresponding pathways and their correlations that can offer new potential insights into the mechanistic basis of this condition.
cryptococcosis 是一种侵袭性真菌病,其患病率呈上升趋势,死亡率非常高,主要由 cryptococcus 引起。然而,其致病机制尚不完全清楚。在本研究中,我们旨在通过高通量测序技术筛选人单核细胞(THP-1)细胞感染()后的 lncRNA 标志物,并探讨其对生物学功能的影响。
我们首先对感染 C. neoformans 的 THP-1 细胞和正常 THP-1 细胞进行了 lncRNA 微阵列分析。基于这些数据,使用 RT-qPCR 验证了所选 lncRNAs 和 mRNAs 的表达。然后进行了功能和途径富集分析。最后,通过基于差异表达 lncRNAs 的 lncRNA 靶标工具进行了靶标预测。
我们使用微阵列确定了 81 个上调和 96 个下调的 lncRNA。此外,分析数据显示 42 个上调和 57 个下调基因,并发现感染调节中神经活性配体-受体相互作用、酪氨酸代谢和苯丙氨酸代谢受到严重损害。99 个差异表达 mRNAs 的 GO 富集分析显示,这些模块表现出不同的信号通路和生物机制,如蛋白质结合和金属离子结合。此外,还分析了 lncRNAs 和 mRNAs 的共表达关系。qRT-PCR 分析证实了 top10 个差异表达 mRNA 和 lincRNA 的表达。通过 RNA-seq 检测了感染后 THP-1 细胞中 lncRNA 的表达,表明微阵列分析可以揭示具有功能意义的 lncRNA,这些 lncRNA 可能与患者病情的进展有关。
本研究分析了感染中的差异 lncRNAs 和 mRNAs,并预测了相应的途径及其相关性,为该疾病的机制基础提供了新的潜在见解。