Electric field promoted odontogenic differentiation of stem cells from apical papilla by remodelling cytoskeleton

被引:0
|
作者
Li, Xiaolin [1 ,2 ]
Zhao, Sanjun [3 ]
Liu, Yao [4 ,5 ,6 ,7 ]
Gu, Yu [8 ,9 ]
Qiu, Lihong [1 ]
Chen, Xu [2 ]
Sloan, Alastair J. [2 ,10 ]
Song, Bing [11 ,12 ,13 ,14 ,15 ]
机构
[1] China Med Univ, Sch Hosp & Stomatol, Dept Endodont, Liaoning Prov Key Lab Oral Dis, Shenyang, Peoples R China
[2] China Med Univ, Sch Hosp & Stomatol, Liaoning Prov Key Lab Oral Dis, Dept Pediat Dent, Shenyang, Peoples R China
[3] Yunnan Normal Univ, Sch Life Sci, Kunming, Peoples R China
[4] Tongji Univ, Shanghai Engn Res Ctr Tooth Restorat & Regenerat, Shanghai, Peoples R China
[5] Tongji Univ, Tongji Res Inst Stomatol, Shanghai, Peoples R China
[6] Tongji Univ, Shanghai Tongji Stomatol Hosp, Dept Pediat Dent, Shanghai, Peoples R China
[7] Tongji Univ, Dent Sch, Shanghai, Peoples R China
[8] Morrello Clin, Neuro Rehabil & Neuro Physiotherapy, Newport, Wales
[9] Cardiff Univ, Cardiff Inst Tissue Engn & Repair, Sch Dent, Cardiff, Wales
[10] Univ Melbourne, Melbourne Dent Sch, Fac Med Dent & Hlth Sci, Melbourne, Vic, Australia
[11] China Med Univ, Hosp 1, Dept Dermatol, Minist Educ,Natl Hlth Commiss,Key Lab Immunodermat, Shenyang, Peoples R China
[12] Shenzhen Univ Adv Technol, Sch Biomed Engn, Shenzhen, Peoples R China
[13] Chinese Acad Sci, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Ctr Translat Med Res & Dev, Shenzhen, Peoples R China
[14] Chinese Acad Sci, Key Lab Biomed Imaging Sci & Syst, Shenzhen, Peoples R China
[15] State Key Lab Biomed Imaging Sci & Syst, Shenzhen, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
stem cells from apical papilla; odontogenic differentiation; dentine regeneration; direct current electric fields; cytoskeleton; TISSUES; MECHANISMS; MIGRATION; MOVEMENT;
D O I
10.1111/iej.14213
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aim This study examined the impact of direct current electric fields (DCEFs) on the biological properties of stem cells derived from the apical papilla (SCAP) and further elucidated the underlying mechanisms involved in odontogenic differentiation induced by DCEFs stimulation. Methodology The measurement of endogenous currents in wounded dentine was achieved using a non-invasive vibrating probe system. Two-dimensional (2D) and three-dimensional (3D) systems were developed to apply DCEFs of varying strengths. The migration direction and trajectories of SCAP within DCEFs were analysed using time-lapse imaging. Cell proliferation was assessed through Hoechst staining and the CCK-8 assay. Changes in cell morphology, arrangement, and polarization were examined using fluorescence staining. The odontogenic differentiation of SCAP in vitro was assessed using quantitative polymerase chain reaction (qPCR), western blot analysis, alkaline phosphatase staining, and Alizarin Red S staining. In vivo evaluation was conducted through Haematoxylin and eosin staining, immunohistochemistry staining, and Sirius Red staining after transplantation experiments. Results Injured dentine demonstrated a significantly increased outward current, and DCEFs facilitated the migration of SCAP towards the anode. DCEFs at a magnitude of 100 mV/mm promoted SCAP proliferation, whereas DCEFs at 200 mV/mm enhanced both polarization and odontogenic differentiation of SCAP. The application of cytoskeletal polymerization inhibitors mitigated the odontogenic differentiation induced by DCEFs. In vivo studies confirmed that DCEFs promoted the differentiation of SCAP into odontoblast-like cells in an orderly arrangement, as well as the formation of collagen fibres and dentine-like tissue. Conclusions DCEFs of varying intensities exhibited an enhanced capacity for migration, proliferation, odontogenic differentiation, and polarization in SCAP. These findings provide substantial insights for the advancement of innovative therapeutic strategies targeting the repair and regeneration of immature permanent teeth and dentine damage.
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页数:17
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