Mi Jun, Wang Shuangshuang, Liu Panpan, Liu Chang, Zhuang Dexuan, Leng Xue, Zhang Qun, Bai Fuxiang, Feng Qiang, Wu Xunwei
Department of Tissue Engineering and Regeneration, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University and Shandong Key Laboratory of Oral Tissue Regeneration and, Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, Jinan, China.
Shenzhen Research Institute of Shandong University, Shenzhen, China.
Front Cell Dev Biol. 2022 Jun 16;10:921663. doi: 10.3389/fcell.2022.921663. eCollection 2022.
Mesenchymal stem cells (MSCs) within the periodontal ligament (PDL), termed periodontal ligament stem cells (PDLSCs), have a self-renewing capability and a multidirectional differentiation potential. The molecular mechanisms that regulate multidirectional differentiation, such as the osteogenic differentiation of PDLSCs, remain to be elucidated. Cullin 4B (CUL4B), which assembles the CUL4B-RING ubiquitin ligase (CRL4B) complex, is involved in regulating a variety of developmental and physiological processes including the skeletal development and stemness of cancer stem cells. However, nothing is known about the possible role of CUL4B in the osteogenic differentiation of PDLSCs. Here, we found that knockdown of CUL4B decreased the proliferation, migration, stemness and osteogenic differentiation ability of PDLSCs. Mechanistically, we demonstrate that CUL4B cooperates with the PRC2 complex to repress the expression of miR-320c and miR-372/373-3p, which results in the upregulation of RUNX2, a master transcription factor (TF) that regulates osteogenic differentiation. In brief, the present study reveals the role of CUL4B as a new regulator of osteogenic differentiation in PDLSCs.
牙周膜(PDL)中的间充质干细胞(MSCs),即牙周膜干细胞(PDLSCs),具有自我更新能力和多向分化潜能。调节多向分化的分子机制,如PDLSCs的成骨分化,仍有待阐明。组装CUL4B-RING泛素连接酶(CRL4B)复合物的Cullin 4B(CUL4B)参与调节包括骨骼发育和癌症干细胞干性在内的多种发育和生理过程。然而,关于CUL4B在PDLSCs成骨分化中可能发挥的作用尚不清楚。在这里,我们发现敲低CUL4B会降低PDLSCs的增殖、迁移、干性和成骨分化能力。从机制上讲,我们证明CUL4B与PRC2复合物协同作用以抑制miR-320c和miR-372/373-3p的表达,这导致RUNX2上调,RUNX2是一种调节成骨分化的主要转录因子(TF)。简而言之,本研究揭示了CUL4B作为PDLSCs成骨分化新调节因子的作用。