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人牙髓干细胞早期牙源性分化过程中的力学变化

Mechanical changes in human dental pulp stem cells during early odontogenic differentiation.

作者信息

Jones Taneka D, Naimipour Hamed, Sun Shan, Cho Michael, Alapati Satish B

机构信息

Department of Bioengineering, University of Illinois at Chicago, Chicago, Illinois.

Department of Endodontics, University of Illinois at Chicago, Chicago, Illinois.

出版信息

J Endod. 2015 Jan;41(1):50-5. doi: 10.1016/j.joen.2014.07.030. Epub 2014 Sep 18.

Abstract

INTRODUCTION

Cell adhesion and migration in bioactive scaffolds require actin cytoskeleton remodeling and focal adhesion formation. Additionally, human dental pulp stem cells (hDPSCs) undergo several changes in their mechanical properties during odontogenic differentiation. The effect of factors essential for odontogenesis on actin stress fiber elasticity and focal adhesion formation is not known.

METHODS

Live hDPSCs cultured in odontogenic media were imaged for cytoskeleton changes using an atomic force microscope. The Young's modulus (kPa) of the cytoskeleton was recorded as a function of culture medium for 10 days. Focal adhesion formation was assessed using immunofluorescence. Cultured hDPSCs were incubated with a monoclonal vinculin antibody, and filamentous actins were visualized using 0.5 μmol/L phalloidin.

RESULTS

Cytoskeletal elasticity significantly increased in response to odontogenic media. Both the number and physical size of focal adhesions in hDPSCs also increased. Up-regulation of vinculin expression was evident. The increase in the formation of focal adhesions was consistent with actin remodeling to stress fibers.

CONCLUSIONS

Our findings suggest that hDPSCs firmly attach to the glass substrate in response to odontogenic media. Successful regeneration of pulp-dentin tissue using biomimetic scaffolds will likely require cell-extracellular matrix interactions influenced by biochemical induction factors.

摘要

引言

生物活性支架中的细胞黏附与迁移需要肌动蛋白细胞骨架重塑和黏着斑形成。此外,人牙髓干细胞(hDPSCs)在牙源性分化过程中其力学性能会发生多种变化。牙源性必需因子对肌动蛋白应力纤维弹性和黏着斑形成的影响尚不清楚。

方法

使用原子力显微镜对在牙源性培养基中培养的活hDPSCs进行成像,以观察细胞骨架变化。记录细胞骨架的杨氏模量(kPa)随培养基培养10天的变化情况。使用免疫荧光评估黏着斑形成。将培养的hDPSCs与单克隆纽蛋白抗体孵育,并用0.5μmol/L鬼笔环肽使丝状肌动蛋白可视化。

结果

响应牙源性培养基,细胞骨架弹性显著增加。hDPSCs中黏着斑的数量和物理尺寸也增加。纽蛋白表达上调明显。黏着斑形成的增加与肌动蛋白重塑为应力纤维一致。

结论

我们的研究结果表明,hDPSCs响应牙源性培养基而牢固地附着于玻璃底物。使用仿生支架成功再生牙髓 - 牙本质组织可能需要受生化诱导因子影响的细胞 - 细胞外基质相互作用。

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