褪黑素
牙周膜干细胞
细胞生物学
炎症
线粒体
化学
干细胞
生物
内分泌学
免疫学
生物化学
碱性磷酸酶
酶
作者
Xuan Li,Bei‐Min Tian,Yuan Yin,Huan Zhou,Dian Gan,Fen Liu,Jiu-Jiu Zhang,Dao‐Kun Deng,Chen Jiao,Ming Xu,Li‐An Wu,X. H. He,Fa‐Ming Chen
标识
DOI:10.1016/j.fmre.2024.05.012
摘要
Inflammation-induced mitochondrial dysfunction functionally impairs periodontal ligament stem cells (PDLSCs) and hinders their therapeutic efficacy in periodontal regeneration. Melatonin, a mitochondrion-targeted molecule, is considered a promising anti-inflammatory agent in therapeutics, but whether melatonin protects PDLSC cementoblastic differentiation against inflammation-induced damage and the underlying mechanisms of this function remain unclear. This study confirmed that melatonin rescues PDLSC cementoblastic differentiation under inflammatory conditions and that melatonin-induced recovery is linked to ameliorated mitochondrial function in cells. Next, through lncRNA microarray analysis, mass spectrometry and functional studies, an interaction between LINC01444 and HSPD1 was identified as a mechanism mediating these melatonin-induced mitochondrial changes. In this context, suppressing LINC01444 was found to increase the total and cytoplasmic HSPD1 protein levels, and in turn, mitochondrial function improved. We further revealed the upstream mechanism by which melatonin inhibits the m6A modification of LINC01444, thereby decreasing its stability and expression. Our data indicate that LINC01444 is a key target involved in the restorative effects of melatonin on cellular mitochondrial function and cementoblastic differentiation. Melatonin inhibits LINC01444 m6A modification to maintain its stability and expression and prevents LINC01444 from interacting with HSPD1 to exert its damaging effects on PDLSCs.
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