Sonic Hedgehog Promotes Cementoblastic Differentiation via Activating the BMP Pathways

被引:17
|
作者
Bae, Won-Jung [1 ,2 ]
Auh, Q-Schick [3 ]
Lim, Hyun-Chang [4 ]
Kim, Gyu-Tae [5 ]
Kim, Hyun-Soo [6 ]
Kim, Eun-Cheol [1 ,2 ]
机构
[1] Kyung Hee Univ, Dept Oral & Maxillofacial Pathol, Sch Dent, 14 Kyungheedae Ro, Seoul 02453, South Korea
[2] Kyung Hee Univ, Res Ctr Tooth & Periodontal Regenerat MRC, 14 Kyungheedae Ro, Seoul 02453, South Korea
[3] Kyung Hee Univ, Sch Dent, Dept Oral Med, Seoul, South Korea
[4] Kyung Hee Univ, Sch Dent, Dept Periodontol, Seoul, South Korea
[5] Kyung Hee Univ, Sch Dent, Dept Oral & Maxillofacial Radiol, Seoul, South Korea
[6] Kyung Hee Univ, Grad Sch, Dept Orthodont, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Sonic hedgehog; Cementoblasts; Differentiation; Signal pathways; BONE MORPHOGENETIC PROTEIN-2; PERIODONTAL-LIGAMENT CELLS; MESENCHYMAL STEM-CELLS; OSTEOBLASTIC DIFFERENTIATION; SIGNALING PATHWAY; GENE-EXPRESSION; TOOTH ROOT; IN-VITRO; PROLIFERATION; CEMENTUM;
D O I
10.1007/s00223-016-0155-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although sonic hedgehog (SHH), an essential molecule in embryogenesis and organogenesis, stimulates proliferation of human periodontal ligament (PDL) stem cells, the effects of recombinant human SHH (rh-SHH) on osteoblastic differentiation are unclear. To reveal the role of SHH in periodontal regeneration, expression of SHH in mouse periodontal tissues and its effects on the osteoblastic/cementoblastic differentiation in human cementoblasts were investigated. SHH is immunolocalized to differentiating cementoblasts, PDL cells, and osteoblasts of the developing mouse periodontium. Addition of rh-SHH increased cell growth, ALP activity, and mineralization nodule formation, and upregulated mRNA expression of osteoblastic and cementoblastic markers. The osteoblastic/cementoblastic differentiation of rh-SHH was abolished by the SHH inhibitor cyclopamine (Cy) and the BMP antagonist noggin. rh-SHH increased the expression of BMP-2 and -4 mRNA, as well as levels of phosphorylated Akt, ERK, p38, and JNK, and of MAPK and NF-kappa B activation, which were reversed by noggin, Cy, and BMP-2 siRNA. Collectively, this study is the first to demonstrate that SHH can promote cell growth and cell osteoblastic/cementoblastic differentiation via BMP pathway. Thus, SHH plays important roles in the development of periodontal tissue, and might represent a new therapeutic target for periodontitis and periodontal regeneration.
引用
收藏
页码:396 / 407
页数:12
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