Neural Differentiation of Human Adipose Tissue-Derived Stem Cells Involves Activation of the Wnt5a/JNK Signalling

被引:39
作者
Jang, Sujeong [1 ]
Park, Jong-Seong [1 ]
Jeong, Han-Seong [1 ]
机构
[1] Chonnam Natl Univ, Dept Physiol, Sch Med, Gwangju 501746, South Korea
基金
新加坡国家研究基金会;
关键词
TRANSPLANTATION; PROLIFERATION; PROMOTES;
D O I
10.1155/2015/178618
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stem cells are a powerful resource for cell-based transplantation therapies, but understanding of stem cell differentiation at the molecular level is not clear yet. We hypothesized that the Wnt pathway controls stem cell maintenance and neural differentiation. We have characterized the transcriptional expression of Wnt during the neural differentiation of hADSCs. After neural induction, the expressions of Wnt2, Wnt4, and Wnt11 were decreased, but the expression of Wnt5a was increased compared with primary hADSCs in RT-PCR analysis. In addition, the expression levels of most Fzds and LRP5/6 ligand were decreased, but not Fzd3 and Fzd5. Furthermore, Dvl1 and RYK expression levels were downregulated in NI-hADSCs. There were no changes in the expression of beta-catenin and GSK3 beta. Interestingly, Wnt5a expression was highly increased in NI-hADSCs by real time RT-PCR analysis and western blot. Wnt5a level was upregulated after neural differentiation and Wnt3, Dvl2, and Naked1 levels were downregulated. Finally, we found that the JNK expression was increased after neural induction and ERK level was decreased. Thus, this study shows for the first time how a single Wnt5a ligand can activate the neural differentiation pathway through the activation of Wnt5a/JNK pathway by binding Fzd3 and Fzd5 and directing Axin/GSK-3 beta in hADSCs.
引用
收藏
页数:7
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共 31 条
[1]   Olig2-Induced Neural Stem Cell Differentiation Involves Downregulation of Wnt Signaling and Induction of Dickkopf-1 Expression [J].
Ahn, Sung-Min ;
Byun, Kyunghee ;
Kim, Deokhoon ;
Lee, Kiyoung ;
Yoo, Jong Shin ;
Kim, Seung U. ;
Jho, Eek-hoon ;
Simpson, Richard J. ;
Lee, Bonghee .
PLOS ONE, 2008, 3 (12)
[2]   Autologous mesenchymal stem cell transplantation in stroke patients [J].
Bang, OY ;
Lee, JS ;
Lee, PH ;
Lee, G .
ANNALS OF NEUROLOGY, 2005, 57 (06) :874-882
[3]   WNT signaling in bone homeostasis and disease: from human mutations to treatments [J].
Baron, Roland ;
Kneissel, Michaela .
NATURE MEDICINE, 2013, 19 (02) :179-192
[4]   Wnt5a Mediates Nerve Growth Factor-Dependent Axonal Branching and Growth in Developing Sympathetic Neurons [J].
Bodmer, Daniel ;
Levine-Wilkinson, Seamus ;
Richmond, Alissa ;
Hirsh, Sarah ;
Kuruvilla, Rejji .
JOURNAL OF NEUROSCIENCE, 2009, 29 (23) :7569-7581
[5]   Autocrine stimulation of osteoblast activity by Wnt5a in response to TNF-α in human mesenchymal stem cells [J].
Briolay, A. ;
Lencel, P. ;
Bessueille, L. ;
Caverzasio, J. ;
Buchet, R. ;
Magne, D. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 430 (03) :1072-1077
[6]   Wnt/β-Catenin Signaling Blockade Promotes Neuronal Induction and Dopaminergic Differentiation in Embryonic Stem Cells [J].
Cajanek, Lukas ;
Ribeiro, Diogo ;
Liste, Isabel ;
Parish, Clare L. ;
Bryja, Vitezslav ;
Arenas, Ernest .
STEM CELLS, 2009, 27 (12) :2917-2927
[7]   Mesodermal fate decisions of a stem cell: the Wnt switch [J].
Davis, L. A. ;
zur Nieden, N. I. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (17) :2658-2674
[8]   Expression profiling and functional analysis of Wnt signaling mechanisms in mesenchymal stem cells [J].
Etheridge, SL ;
Spencer, GJ ;
Heath, DJ ;
Genever, PG .
STEM CELLS, 2004, 22 (05) :849-860
[9]   Wnt-5a/JNK Signaling Promotes the Clustering of PSD-95 in Hippocampal Neurons [J].
Farias, Ginny G. ;
Alfaro, Ivan E. ;
Cerpa, Waldo ;
Grabowski, Catalina P. ;
Godoy, Juan A. ;
Bonansco, Christian ;
Inestrosa, Nibaldo C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (23) :15857-15866
[10]   Differentiation of human neural progenitor cells regulated by Wnt-3a [J].
Huebner, Rayk ;
Schmoele, Anne-Caroline ;
Liedmann, Andrea ;
Frech, Moritz J. ;
Rolls, Arndt ;
Luo, Jiankai .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 400 (03) :358-362