Mineral trioxide aggregate immersed in sodium hypochlorite reduce the osteoblastic differentiation of human periodontal ligament stem cells.
Mineral trioxide aggregate immersed in sodium hypochlorite reduce the osteoblastic differentiation of human periodontal ligament stem cells.
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DOI:
10.1038/s41598-021-01545-3
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发表时间:
2021-11-11
影响因子:
4.6
通讯作者:
Maeda H
中科院分区:
文献类型:
--
作者:
Yamashita K;Tomokiyo A;Ono T;Ipposhi K;Alhasan MA;Tsuchiya A;Hamano S;Sugii H;Yoshida S;Itoyama T;Maeda H
White mineral trioxide aggregate (WMTA) is a root canal treatment material, which is known to exhibit a dark brown color when in contact with sodium hypochlorite solution (NaOCl). This study aimed to investigate the effects of NaOCl on the surface properties of WMTA discs and WMTA-induced osteoblastic differentiation of periodontal ligament stem cells (PDLSCs). Mixed WMTA (ProRoot MTA) was filled into the molds to form WMTA discs. These discs were immersed in distilled water (D-WMTA) or 5% NaOCl (Na-WMTA). Their surface structures and Ca2+ release level was investigated. Moreover, they were cultured with a clonal human PDLSC line (line 1–17 cells). The main crystal structures of Na-WMTA were identical to the structures of D-WMTA. Globular aggregates with polygonal and needle-like crystals were found on D-WMTA and Na-WMTA, which included Ca, Si, Al, C and O. However, many amorphous structures were also identified on Na-WMTA. These structures consisted of Na and Cl, but did not include Ca. NaOCl immersion also reduced Ca2+ release level from whole WMTA discs. Line 1–17 cells cultured with D-WMTA formed many mineralized nodules and exhibited high expression levels of osteoblast-related genes. However, cells incubated with Na-WMTA generated a small number of nodules and showed low expression levels of osteoblast-related genes. These results indicated that NaOCl reduced Ca2+ release from WMTA by generating amorphous structures and changing its elemental distribution. NaOCl may also partially abolish the ability of WMTA to stimulate osteoblastic differentiation of PDLSCs.
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影响因子:
4.3
作者:
Tomokiyo A;Yoshida S;Hamano S;Hasegawa D;Sugii H;Maeda H
通讯作者:
Maeda H
影响因子:
1.3
作者:
Garna, Devy;Kaur, Manmeet;Ghuman, Mandeep
通讯作者:
Ghuman, Mandeep
影响因子:
168.9
作者:
Seo, BM;Miura, M;Shi, ST
通讯作者:
Shi, ST
影响因子:
5
作者:
Silva, R. A. B.;Borges, A. T. N.;Silva, L. A. B.
通讯作者:
Silva, L. A. B.
影响因子:
4.2
作者:
Tang, HM;Torabinejad, M;Kettering, JD
通讯作者:
Kettering, JD