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静磁场可提高无二甲亚砜冷冻保存期间牙髓干细胞的存活率。

Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation.

作者信息

Lin Shu-Li, Chang Wei-Jen, Lin Chun-Yen, Hsieh Sung-Chih, Lee Sheng-Yang, Fan Kang-Hsin, Lin Che-Tong, Huang Haw-Ming

机构信息

a Dental Department , Cathay General Hospital , Taipei , Taiwan .

b School of Dentistry, College of Oral Medicine, Taipei Medical University , Taipei , Taiwan .

出版信息

Electromagn Biol Med. 2015;34(4):302-8. doi: 10.3109/15368378.2014.919588. Epub 2014 May 23.

Abstract

Successful and efficient cryopreservation of living cells and organs is a key clinical application of regenerative medicine. Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective effects of static magnetic fields (SMFs) on human dental pulp stem cells (DPSCs) during cryopreservation. Human DPSCs isolated from extracted teeth were frozen with a 0.4-T or 0.8-T SMF and then stored at -196 °C for 24 h. During freezing, the cells were suspended in freezing media containing with 0, 3 or 10% DMSO. After thawing, the changes in survival rate of the DPSCs were determined by flow cytometry. To understand the possible cryoprotective mechanisms of the SMF, the membrane fluidity of SMF-exposed DPSCs was tested. The results showed that when the freezing medium was DMSO-free, the survival rates of the thawed DPSCs increased 2- or 2.5-fold when the cells were exposed to 0.4-T or 0.8-T SMFs, respectively (p < 0.01). In addition, after exposure to the 0.4-T SMF, the fluorescence anisotropy of the DPSCs increased significantly (p < 0.01) in the hydrophilic region. These results show that SMF exposure improved DMSO-free cryopreservation. This phenomenon may be due to the improvement of membrane stability for resisting damage caused by ice crystals during the freezing procedure.

摘要

活细胞和器官的成功高效冷冻保存是再生医学的一项关键临床应用。最近,已有关于完整牙库及牙组织冷冻保存的磁冷冻保存报道。本研究的目的是评估静态磁场(SMF)在冷冻保存过程中对人牙髓干细胞(DPSC)的冷冻保护作用。从拔除的牙齿中分离出的人DPSC用0.4-T或0.8-T的SMF进行冷冻,然后在-196°C下保存24小时。冷冻过程中,细胞悬浮于含有0、3或10%二甲基亚砜(DMSO)的冷冻培养基中。解冻后,通过流式细胞术测定DPSC的存活率变化。为了解SMF可能的冷冻保护机制,对暴露于SMF的DPSC的膜流动性进行了检测。结果表明,当冷冻培养基不含DMSO时,细胞分别暴露于0.4-T或0.8-T的SMF时,解冻后DPSC的存活率分别提高了2倍或2.5倍(p<0.01)。此外,暴露于0.4-T的SMF后,DPSC在亲水区的荧光各向异性显著增加(p<0.01)。这些结果表明,暴露于SMF可改善无DMSO的冷冻保存。这种现象可能是由于在冷冻过程中膜稳定性提高,从而抵抗了冰晶造成的损伤。

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