An in vitro study of the impact of 4mT static magnetic field to modify the differentiation rate of rat bone marrow stem cells into primordial germ cells

被引:24
作者
Jouni, Fatemeh Javani [1 ]
Abdolmaleki, Parviz [1 ]
Behmanesh, Mehrdad [2 ]
Movahedin, Mansoureh [3 ]
机构
[1] TMU, Fac Biol Sci, Dept Biophys, Tehran, Iran
[2] TMU, Fac Biol Sci, Dept Genet, Tehran, Iran
[3] TMU, Fac Med Sci, Dept Anat Sci, Tehran, Iran
基金
美国国家科学基金会;
关键词
Bone marrow stem cell; Bone morphogenetic protein 4; Differentiation; Primordial germ cell; Static magnetic field; EMBRYONIC STEM; GENE-EXPRESSION; VICIA-FABA; SELF-RENEWAL; PROTEIN; ISOFORMS; OCT4; GENERATION; INDUCTION; KNOCKDOWN;
D O I
10.1016/j.diff.2014.06.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This investigation was performed to evaluate the differentiation capacity and alteration in genes expression patterns during in vitro differentiation of bone marrow stem cells into primordial germ cells using static magnetic held (4 mT) and BMP-4 (25 ng/ml). The rate of differentiation was investigated using the Real Time-PCR method for tracing expression of differentiation markers (Oct-4, Nanog, C-Myc, Fragilis, Mvh and Stella). Then, immunocytochemical reaction was carried out for detection of marker proteins (Oct4 and Mvh). Increasing of the exposure time of the 4 mT SMF (24 and 48 h) and treatment time with 25 ng/ml BMP4 (48 and 96 h) indicated a marked decrease in expression of pluripotency genes (Oct-4, Nanog and C-Myc) and Oct4 protein and increase in primordial germ cell specific genes (Fragilis, Mvh and Stella) and Mvh protein compared with the control group. Final results showed that in a synergistic manner, the combination of SWF with BMP4 exaggerates the differentiation potential of BMSCs to PGCs by activating the MAPK pathway and altering the Ca2+ concentration. (C) 2014 International Society of Differentiation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:230 / 237
页数:8
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