West China Journal of Stomatology ›› 2025, Vol. 43 ›› Issue (2): 183-189.doi: 10.7518/hxkq.2025.2024392

• Basic Research • Previous Articles     Next Articles

Effects of cell area on single odontoblast polarization and differentiation via microarray technology

Li Huen1,2(), Yu Nianzuo3,4(), Li Xiheng1,2, Tang Xiaoduo2,3, Sun Yalu1,2, Si Chao1,2, Zhang Junhu3,4(), Chang Bei1,2()   

  1. 1.Dept. of Pediatric Dentistry, Hospital of Stomatology, Jilin University, Changchun 130021, China
    2.Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, Changchun 130021, China
    3.Institute of Translational Medicine, The First Hospital of Jilin University, Changchun 130021, China
    4.College of Chemistry, Jilin University, State Key Laboratory of Supramolecular Structure and Materials, Changchun 130021, China
  • Received:2024-10-24 Revised:2025-02-17 Online:2025-04-01 Published:2025-03-25
  • Contact: Zhang Junhu,Chang Bei E-mail:lhe22@mails.jlu.edu.cn;ynz@jlu.edu.cn;zjh@jlu.edu.cn;bchang@jlu.edu.cn
  • Supported by:
    Natural Science Foundation of China(82101075);Young Elite Scientists Sponsorship Program by China Association for Science and Technology(YESS20210407);China Postdoctoral Science Foundation(2022M711301);Bethune Project of Jilin University(419161923025)

Abstract:

Objective This study aimed to explore the impact of cell spreading area on odontoblast polarization and differentiation using micropatterned surfaces ge-nerated by photolithography. Methods Micropatterned surfaces with differential adhesive properties were prepared using polyethylene glycol diacrylate (PEGDA)-ba-sed photolithography. Human dental pulp stem cells (hD-PSCs) were isolated into single cells and cultured on micropatterned surfaces with areas of 1 800, 2 700, and 3 600 μm2. Immunofluorescence staining was used to observe cell morphology and analyze the relocating of the golgi apparatus and nucleus. Alkaline phosphatase staining was preformed to examine odontogenic differentiation. Results The hDPSCs were successfully isolated and cultured on micropatterned surfaces mimicking the morphology of polarized odontoblasts. Phalloidin staining confirmed that the isolated hDPSCs successfully recapitulated the morphology of predesigned micropatterns. Immunofluorescence staining showed that the polarization and differentiation levels of the hDPSCs with a 3600 μm2 area were significantly higher than those with 1 800 and 2 700 μm2 areas (P<0.05). Conclusion The polarization and differentiation of single hDPSCs increased with the cell areas on micropatterned surfaces.

Key words: cell polarization, micropatterning, odontoblast, cell differentiation

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