The State Key Laboratory Breeding Base of Basic Science of Stomatology and Key Laboratory for Oral Biomedicine of Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, China.
Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan 430071, China.
Development. 2023 May 15;150(10). doi: 10.1242/dev.200848. Epub 2023 May 22.
Dentin is the major hard tissue of teeth formed by differentiated odontoblasts. How odontoblast differentiation is regulated remains enigmatic. Here, we report that the E3 ubiquitin ligase CHIP is highly expressed in undifferentiated dental mesenchymal cells and downregulated after differentiation of odontoblasts. Ectopic expression of CHIP inhibits odontoblastic differentiation of mouse dental papilla cells, whereas knockdown of endogenous CHIP has opposite effects. Chip (Stub1) knockout mice display increased formation of dentin and enhanced expression of odontoblast differentiation markers. Mechanistically, CHIP interacts with and induces K63 polyubiquitylation of the transcription factor DLX3, leading to its proteasomal degradation. Knockdown of DLX3 reverses the enhanced odontoblastic differentiation caused by knockdown of CHIP. These results suggest that CHIP inhibits odontoblast differentiation by targeting its tooth-specific substrate DLX3. Furthermore, our results indicate that CHIP competes with another E3 ubiquitin ligase, MDM2, that promotes odontoblast differentiation by monoubiquitylating DLX3. Our findings suggest that the two E3 ubiquitin ligases CHIP and MDM2 reciprocally regulate DLX3 activity by catalyzing distinct types of ubiquitylation, and reveal an important mechanism by which differentiation of odontoblasts is delicately regulated by divergent post-translational modifications.
牙本质是由分化的成牙本质细胞形成的主要硬组织。成牙本质细胞分化是如何调节的仍然是个谜。在这里,我们报告 E3 泛素连接酶 CHIP 在未分化的牙间充质细胞中高度表达,并在成牙本质细胞分化后下调。CHIP 的异位表达抑制小鼠牙髓细胞的成牙本质细胞分化,而内源性 CHIP 的敲低则有相反的效果。Chip(Stub1)敲除小鼠表现出更多的牙本质形成和增强的成牙本质细胞分化标志物表达。在机制上,CHIP 与转录因子 DLX3 相互作用,并诱导其 K63 多泛素化,导致其蛋白酶体降解。DLX3 的敲低逆转了 CHIP 敲低引起的增强的成牙本质细胞分化。这些结果表明 CHIP 通过靶向其牙齿特异性底物 DLX3 抑制成牙本质细胞分化。此外,我们的结果表明,E3 泛素连接酶 CHIP 和 MDM2 相互竞争,后者通过单泛素化 DLX3 促进成牙本质细胞分化。我们的发现表明,这两种 E3 泛素连接酶 CHIP 和 MDM2 通过催化不同类型的泛素化,相互调节 DLX3 的活性,并揭示了成牙本质细胞分化是如何通过不同的翻译后修饰精细调节的重要机制。