RETRACTED: Polyphosphate induces matrix metalloproteinase-3-mediated proliferation of odontoblast-like cells derived from induced pluripotent stem cells (Retracted article. See vol. 398, 2021)

被引:12
|
作者
Ozeki, Nobuaki [1 ]
Hase, Naoko [1 ]
Yamaguchi, Hideyuki [1 ]
Hiyama, Taiki [1 ]
Kawai, Rie [1 ]
Kondo, Ayami [2 ]
Nakata, Kazuhiko [1 ]
Mogi, Makio [2 ]
机构
[1] Aichi Gakuin Univ, Sch Dent, Dept Endodont, Chikusa Ku, Nagoya, Aichi 4648651, Japan
[2] Aichi Gakuin Univ, Sch Pharm, Dept Med Biochem, Chikusa Ku, Nagoya, Aichi 4648650, Japan
关键词
Inorganic polyphosphate; Matrix metalloproteinase-3; Induced pluripotent stem cell; Odontoblast; Cell proliferation; INORGANIC POLYPHOSPHATE; TNF-ALPHA; DIFFERENTIATION; INDUCTION; PERIODONTITIS; ACTIVATION; EXPRESSION; PROCOLLAGENASE; MINERALIZATION; CALCIFICATION;
D O I
10.1016/j.yexcr.2015.01.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inorganic polyphosphate [Poly(P)] may represent a physiological source of phosphate and has the ability to induce bone differentiation in osteoblasts. We previously reported that cytokine-induced matrix metalloproteinase (MMP)-3 accelerates the proliferation of purified odontoblast-like cells. In this study, MMP-3 small interfering RNA (siRNA) was transfected into odontoblast-like cells derived from induced pluripotent stem cells to investigate whether MMP-3 activity is induced by Poly(P) and/or is associated with cell proliferation and differentiation into odontoblast-like cells. Treatment with Poly(P) led to an increase in both cell proliferation and additional odontoblastic differentiation. Poly(P)-treated cells showed a small but significant increase in dentin sialophosphoprotein (DSPP) and dentin matrix protein-1 (DMP-1) mRNA expression, which are markers of mature odontoblasts. The cells also acquired additional odontoblast-specific properties including adoption of an odontoblastic phenotype typified by high alkaline phosphatase (ALP) activity and a calcification capacity. In addition, Poly(P) induced expression of MMP-3 mRNA and protein, and increased MMP-3 activity. MMP-3 siRNA-mediated disruption of the expression of these effectors potently suppressed the expression of odontoblastic biomarkers ALP, DSPP, and DMP-1, and blocked calcification. Interestingly, upon siRNA-mediated silencing of MMP-3, we noted a potent and significant decrease in cell proliferation. Using specific siRNAs, we revealed that a unique signaling cascade, Poly(P)-->MMP-3-->DSPP and/or DMP-1, was intimately involved in the proliferation of odontoblast-like cells. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:303 / 315
页数:13
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