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WWP2通过单泛素化KLF5促进成牙本质细胞分化。

WWP2 Promotes Odontoblastic Differentiation by Monoubiquitinating KLF5.

作者信息

Fu J, Zheng H, Xue Y, Jin R, Yang G, Chen Z, Yuan G

机构信息

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, HuBei, China.

出版信息

J Dent Res. 2021 Apr;100(4):432-439. doi: 10.1177/0022034520970866. Epub 2020 Nov 9.

Abstract

WW domain-containing E3 Ub-protein ligase 2 (WWP2) belongs to the homologous to E6AP C-terminus (HECT) E3 ligase family. It has been explored to regulate osteogenic differentiation, chondrogenesis, and palatogenesis. Odontoblasts are terminally differentiated mesenchymal cells, which contribute to dentin formation in tooth development. However, it remained unknown whether WWP2 participated in odontoblast differentiation. In this study, WWP2 was found to be expressed in mouse dental papilla cells (mDPCs), odontoblasts, and odontoblastic-induced mDPCs by immunohistochemistry and Western blotting. Besides, WWP2 expression was decreased in the cytoplasm but increased in the nuclei of differentiation-induced mDPCs. When was knocked down, the elevated expression of odontoblast marker genes ( and ) in mDPCs induced by differentiation medium was suppressed. Meanwhile, a decrease of alkaline phosphatase (ALP) activity was observed by ALP staining, and reduced formation of mineralized matrix nodules was demonstrated by Alizarin Red S staining. Overexpression of WWP2 presented opposite results to knockdown experiments, suggesting that WWP2 promoted odontoblastic differentiation of mDPCs. Further investigation found that WWP2 was coexpressed and interacted with KLF5 in the nuclei, leading to ubiquitination of KLF5. The PPPSY (PY2) motif of KLF5 was essential for its physical binding with WWP2. Also, cysteine 838 (Cys838) of WWP2 was the active site for ubiquitination of KLF5, which did not lead to proteolysis of KLF5. Then, KLF5 was confirmed to be monoubiquitinated and transactivated by WWP2, which promoted the expression of KLF5 downstream genes and . Deletion of the PY2 motif of KLF5 or mutation of Cys838 of WWP2 reduced the upregulation of and . Besides, lysine (K) residues K31, K52, K83, and K265 of KLF5 were verified to be crucial to WWP2-mediated KLF5 transactivation. Taken together, WWP2 promoted odontoblastic differentiation by monoubiquitinating KLF5.

摘要

含WW结构域的E3泛素蛋白连接酶2(WWP2)属于E6相关蛋白C端同源(HECT)E3连接酶家族。它已被研究用于调节成骨分化、软骨形成和腭裂发生。成牙本质细胞是终末分化的间充质细胞,在牙齿发育中有助于牙本质形成。然而,WWP2是否参与成牙本质细胞分化仍不清楚。在本研究中,通过免疫组织化学和蛋白质印迹法发现WWP2在小鼠牙乳头细胞(mDPCs)、成牙本质细胞和成牙本质细胞诱导的mDPCs中表达。此外,在分化诱导的mDPCs中,WWP2在细胞质中的表达降低,但在细胞核中的表达增加。当WWP2被敲低时,分化培养基诱导的mDPCs中成牙本质细胞标记基因(和)的表达升高受到抑制。同时,通过碱性磷酸酶(ALP)染色观察到ALP活性降低,茜素红S染色显示矿化基质结节形成减少。WWP2过表达呈现出与敲低实验相反的结果,表明WWP2促进了mDPCs的成牙本质细胞分化。进一步研究发现,WWP2在细胞核中与KLF5共表达并相互作用,导致KLF5泛素化。KLF5的PPPSY(PY2)基序对其与WWP2的物理结合至关重要。此外,WWP2的半胱氨酸838(Cys838)是KLF5泛素化的活性位点,这不会导致KLF5的蛋白水解。然后,证实KLF5被WWP2单泛素化并反式激活,这促进了KLF5下游基因和的表达。KLF5的PY2基序缺失或WWP2的Cys838突变降低了和的上调。此外,可以证实KLF5的赖氨酸(K)残基K31、K52、K83和K265对WWP2介导的KLF5反式激活至关重要。综上所述,WWP2通过单泛素化KLF5促进成牙本质细胞分化。

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