Reduction of inflammation in a chronic periodontitis model in rats by TNF-α gene silencing with a topically applied siRNA-loaded calcium phosphate paste

被引:23
作者
Tenkumo, Taichi [1 ]
Rojas-Sanchez, Leonardo [2 ,3 ]
Saenz, Juan Ramon Vanegas [4 ]
Ogawa, Toru [1 ]
Miyashita, Makiko [1 ]
Yoda, Nobuhiro [1 ]
Prymak, Oleg [2 ,3 ]
Sokolova, Viktoriya [2 ,3 ]
Sasaki, Keiichi [1 ]
Epple, Matthias [2 ,3 ]
机构
[1] Tohoku Univ, Grad Sch Dent, Div Adv Prosthet Dent, Aoba Ku, 4-1 Seiryo Machi, Sendai, Miyagi 9808575, Japan
[2] Univ Duisburg Essen, Inorgan Chem, Univ Str 5-7, D-45117 Essen, Germany
[3] Univ Duisburg Essen, Ctr Nanointegrat Duisburg Essen CeNIDE, Univ Str 5-7, D-45117 Essen, Germany
[4] Univ Amer UAM, Costado Noroeste Camino Oriente, Fac Odontol, Mat Dentales, Managua, Nicaragua
基金
日本学术振兴会;
关键词
Calcium phosphate; Nanoparticles; Gene silencing; TNF-alpha; Periodontitis; Anti-inflammation; IN-VIVO; NUCLEIC-ACIDS; NANOPARTICLES; TRANSFECTION; DELIVERY; DNA; MACROPHAGES; EXPRESSION; CARRIERS; RELEASE;
D O I
10.1016/j.actbio.2020.01.031
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We developed a calcium phosphate-based paste containing siRNA against TNF-alpha and investigated its anti-inflammatory and bone-healing effects in vitro and in vivo in a rat periodontitis model. The bioactive spherical CaPIPElisiRNA/SiO2 nanoparticles had a core diameter of 40-90 nm and a positive charge (+23 mV) that facilitated cellular uptake. The TNF-alpha gene silencing efficiency of the nanoparticles in J774.2 monocytes, gingival-derived cells, and bone marrow-derived cells was 12 +/- 2%, 36 +/- 8%, and 35 +/- 22%, respectively. CaP/PElisiRNA/SiO2 nanoparticles cancelled the suppression of alkaline phosphatase (ALP) activity in LPS-stimulated bone marrow-derived cells. In vivo, ALP mRNA was up-regulated, TNF-alpha mRNA was down-regulated, and the amount of released TNF-alpha was significantly reduced after topical application of the calcium phosphate-based paste containing siRNA-loaded nanoparticles. The number of TNF-alpha-positive cells in response to CaP/PElisiRNA/SiO2 nanoparticle application was lower than that observed in the absence of siRNA. Elevated ALP activity and numerous TRAP-positive cells (osteoclasts) were observed in response to the application of all calcium phosphate pastes. These results demonstrate that local application of a paste consisting of siRNA-loaded calcium phosphate nanoparticles successfully induces TNF-alpha silencing in vitro and in vivo and removes the suppression of ALP activity stimulated by inflammation. Statement of significance We developed a calcium phosphate-based paste containing nanoparticles loaded with siRNA against TNF-alpha. The nanoparticles had a core diameter of 40-90 nm and positive charge (+23 my). The antiinflammatory and osteoinductive effects of the paste were investigated in vitro and in vivo in a rat periodontitis model. In vitro, the TNF-alpha gene silencing efficiency of the nanoparticles in J774.2 monocytes, gingival-derived cells, and bone marrow-derived cells was 12 +/- 2%, 36 +/- 8%. and 35 +/- 22%, respectively. The ALP activity of bone marrow-derived cells was recovered. In vivo, TNF-alpha mRNA was down-regulated and the amount of released TNF-alpha was significantly reduced, whereas the ALP mRNA was up-regulated. Elevated ALP activity and TRAP-positive cells were observed by immunohistochemistry. (C) 2020 Published by Elsevier Ltd on behalf of Acta Materialia Inc.
引用
收藏
页码:263 / 279
页数:17
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