Panahipour Layla, Imani Atefe, Dos Santos Sanches Natália, Kühtreiber Hannes, Mildner Michael, Gruber Reinhard
Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.
Department of Diagnosis and Surgery, Araçatuba Dental School of Sao Paulo, Sao Paulo 16015-050, Brazil.
Bioengineering (Basel). 2024 Dec 23;11(12):1307. doi: 10.3390/bioengineering11121307.
Hyaluronic acid was proposed to support soft tissue recession surgery and guided tissue regeneration. The molecular mechanisms through which hyaluronic acid modulates the response of connective tissue cells remain elusive. To elucidate the impact of hyaluronic acid on the connective tissue cells, we used bulk RNA sequencing to determine the changes in the genetic signature of gingival fibroblasts exposed to 1.6% cross-linked hyaluronic acid and 0.2% natural hyaluronic acid. Transcriptome-wide changes were modest. Even when implementing a minimum of 1.5 log2 fold-change and a significance threshold of 1.0 -log10, only a dozenth of genes were differentially expressed. Upregulated genes were PLK3, SLC16A6, IL6, HBEGF, DGKE, DUSP4, PTGS2, FOXC2, ATAD2B, NFATC2, and downregulated genes were MMP24 and PLXNA2. RT-PCR analysis supported the impact of hyaluronic acid on increasing the expression of a selected gene panel. The findings from bulk RNA sequencing suggest that gingival fibroblasts experience weak changes in their transcriptome when exposed to hyaluronic acid.
透明质酸被认为可支持软组织退缩手术和引导组织再生。透明质酸调节结缔组织细胞反应的分子机制仍不清楚。为了阐明透明质酸对结缔组织细胞的影响,我们使用批量RNA测序来确定暴露于1.6%交联透明质酸和0.2%天然透明质酸的牙龈成纤维细胞基因特征的变化。全转录组变化不大。即使采用至少1.5的log2倍数变化和1.0 -log10的显著性阈值,也只有十二分之一的基因差异表达。上调的基因有PLK3、SLC16A6、IL6、HBEGF、DGKE、DUSP4、PTGS2、FOXC2、ATAD2B、NFATC2,下调的基因有MMP24和PLXNA2。RT-PCR分析支持透明质酸对增加选定基因表达的影响。批量RNA测序结果表明,牙龈成纤维细胞在暴露于透明质酸时,其转录组变化微弱。