Yao Amin, Zhang Yu, Ouyang Mengting, Wen Lei, Lai Wei
Department of Dermatology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Dermato-Venereology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.
Photochem Photobiol. 2025 Mar-Apr;101(2):505-516. doi: 10.1111/php.14015. Epub 2024 Aug 30.
Transfer RNA-derived small RNAs (tsRNAs) refer to a newly established family of non-coding RNAs that regulate a diverse set of biological processes. However, the function of tsRNAs in skin photoaging remains unclear. This research aims to investigate the potential correlation between tsRNAs and skin photoaging. Human dermal fibroblasts (HDFs) were irradiated with UVA at 10 J/cm once a day lasting for 14 days, resulting in the establishment of a photoaging model induced by UVA. To identify the expression profiles and functions of tsRNAs, tsRNA sequencing and bioinformatics analysis were conducted. qPCR was employed to validate the results of differentially expressed (DE) tsRNAs. A total of 34 tsRNAs exhibited significant differential expression between the UVA and control groups (n = 3), with nine upregulated and 25 downregulated (log fold change >1.5, p-value <0.05). Six tsRNAs were selected at random and validated by qRT-PCR. The enrichment analysis of DE tsRNAs target genes indicated that the dysregulated tsRNAs appeared to be connected with cell cycle, DNA replication and the AGE-RAGE signaling pathway. The expression of tsRNAs was found to be aberrant in UVA-HDF. These findings provide insights into the UVA-induced damage and potential target genes for skin photoaging.
转运RNA衍生的小RNA(tsRNAs)是指一个新建立的非编码RNA家族,其可调节多种生物过程。然而,tsRNAs在皮肤光老化中的功能仍不清楚。本研究旨在探讨tsRNAs与皮肤光老化之间的潜在相关性。将人皮肤成纤维细胞(HDFs)每天用10 J/cm的UVA照射一次,持续14天,从而建立UVA诱导的光老化模型。为了鉴定tsRNAs的表达谱和功能,进行了tsRNA测序和生物信息学分析。采用qPCR验证差异表达(DE)tsRNAs的结果。在UVA组和对照组(n = 3)之间共有34种tsRNAs表现出显著差异表达,其中9种上调,25种下调(log倍数变化>1.5,p值<0.05)。随机选择6种tsRNAs并通过qRT-PCR进行验证。DE tsRNAs靶基因的富集分析表明,失调的tsRNAs似乎与细胞周期、DNA复制和AGE-RAGE信号通路有关。发现tsRNAs在UVA-HDF中的表达异常。这些发现为UVA诱导的皮肤光老化损伤和潜在靶基因提供了见解。