Electromagnetic Fields Mediate Efficient Cell Reprogramming into a Pluripotent State

被引:72
作者
Baek, Soonbong [1 ]
Quan, Xiaoyuan [1 ]
Kim, Soochan [2 ]
Lengner, Christopher [3 ]
Park, Jung-Keug [4 ]
Kim, Jongpil [1 ]
机构
[1] Dongguk Univ, Dept Biomed Engn, Lab Stem Cells & Cell Reprogramming, Seoul 100715, South Korea
[2] Dongguk Univ, Res Inst Biotechnol, Seoul 100715, South Korea
[3] Hankyong Natl Univ, Dept Elect & Elect Engn, Kyonggi Do 456749, South Korea
[4] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
基金
新加坡国家研究基金会;
关键词
electromagnetic fields; cell reprogamming; epigenetic changes; STEM-CELLS; DEFINED FACTORS; MAGNETIC-FIELD; SOMATIC-CELLS; IN-VITRO; DIFFERENTIATION; INDUCTION; EXPOSURE; DISEASE; FIBROBLASTS;
D O I
10.1021/nn502923s
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Life on Earth is constantly exposed to natural electromagnetic fields (EMFs), and it is generally accepted that EMFs may exert a variety of effects on biological systems. Particularly, extremely low-frequency electromagnetic fields (EL-EMFs) affect biological processes such as cell development and differentiation; however, the fundamental mechanisms by which EMFs influence these processes remain unclear. Here we show that EMF exposure induces epigenetic changes that promote efficient somatic cell reprogramming to pluripotency. These epigenetic changes resulted from EMF-induced activation of the histone lysine methyltransferase Mll2. Remarkably, an EMF-free system that eliminates Earth's naturally occurring magnetic field abrogates these epigenetic changes, resulting in a failure to undergo reprogramming. Therefore, our results reveal that EMF directly regulates dynamic epigenetic changes through Mll2, providing an efficient tool for epigenetic reprogramming including the acquisition of pluripotency.
引用
收藏
页码:10125 / 10138
页数:14
相关论文
共 46 条
[1]
An Guang-zhou, 2013, Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi, V31, P246
[2]
Transient JMJD2B-Mediated Reduction of H3K9me3 Levels Improves Reprogramming of Embryonic Stem Cells into Cloned Embryos [J].
Antony, Jisha ;
Oback, Fleur ;
Chamley, Larry W. ;
Oback, Bjoern ;
Laible, Goetz .
MOLECULAR AND CELLULAR BIOLOGY, 2013, 33 (05) :974-983
[3]
Electromagnetic Field Treatment Protects Against and Reverses Cognitive Impairment in Alzheimer's Disease Mice [J].
Arendash, Gary W. ;
Sanchez-Ramos, Juan ;
Mori, Takashi ;
Mamcarz, Malgorzata ;
Lin, Xiaoyang ;
Runfeldt, Melissa ;
Wang, Li ;
Zhang, Guixin ;
Sava, Vasyl ;
Tan, Jun ;
Cao, Chuanhai .
JOURNAL OF ALZHEIMERS DISEASE, 2010, 19 (01) :191-210
[4]
BAKHMUTSKY NG, 1991, SOV MEDITISINA, P86
[5]
915 MHz microwaves and 50 Hz magnetic field affect chromatin conformation and 53BP1 foci in human lymphocytes from hypersensitive and healthy persons [J].
Belyaev, IY ;
Hillert, L ;
Protopopova, M ;
Tamm, C ;
Malmgren, LOG ;
Persson, BRR ;
Selivanova, G ;
Harms-Ringdahl, M .
BIOELECTROMAGNETICS, 2005, 26 (03) :173-184
[6]
Problems of weak electromagnetic field effects in cell biology [J].
Berg, H .
BIOELECTROCHEMISTRY AND BIOENERGETICS, 1999, 48 (02) :355-360
[7]
Experimental evidence of a potentially increased thrombo-embolic disease risk by domestic electromagnetic field exposure [J].
Caprani, A ;
Richert, A ;
Flaud, P .
BIOELECTROMAGNETICS, 2004, 25 (04) :313-315
[8]
Reprogramming of murine and human somatic cells using a single polycistronic vector [J].
Carey, Bryce W. ;
Markoulaki, Styliani ;
Hanna, Jacob ;
Saha, Kris ;
Gao, Qing ;
Mitalipova, Maisam ;
Jaenisch, Rudolf .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (01) :157-162
[9]
A Comparative Analysis of the In Vitro Effects of Pulsed Electromagnetic Field Treatment on Osteogenic Differentiation of Two Different Mesenchymal Cell Lineages [J].
Ceccarelli, Gabriele ;
Bloise, Nora ;
Mantelli, Melissa ;
Gastaldi, Giulia ;
Fassina, Lorenzo ;
De Angelis, Maria Gabriella Cusella ;
Ferrari, Davide ;
Imbriani, Marcello ;
Visai, Livia .
BIORESEARCH OPEN ACCESS, 2013, 2 (04) :283-294
[10]
H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs [J].
Chen, Jiekai ;
Liu, He ;
Liu, Jing ;
Qi, Jing ;
Wei, Bei ;
Yang, Jiaqi ;
Liang, Hanquan ;
Chen, You ;
Chen, Jing ;
Wu, Yaran ;
Guo, Lin ;
Zhu, Jieying ;
Zhao, Xiangjie ;
Peng, Tianran ;
Zhang, Yixin ;
Chen, Shen ;
Li, Xuejia ;
Li, Dongwei ;
Wang, Tao ;
Pei, Duanqing .
NATURE GENETICS, 2013, 45 (01) :34-U62