Wnt signaling promotes neuronal differentiation from mesenchymal stem cells through activation of Tlx3.

Wnt signaling promotes neuronal differentiation from mesenchymal stem cells through activation of Tlx3.
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DOI:
10.1002/stem.624
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发表时间:
2011-05
期刊:
影响因子:
5.2
通讯作者:
Hashino, Eri
Hashino, Eri
中科院分区:
医学2区
文献类型:
--
作者:
Kondo, Takako;Matsuoka, Akihiro J.;Shimomura, Atsushi;Koehler, Karl R.;Chan, Rebecca J.;Miller, Josef M.;Srour, Edward F.;Hashino, Eri

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Wnt/β-catenin signaling promotes neural differentiation by activation of the neuron-specific transcription factors, Neurogenin1 (Ngn1), NeuroD and Brn3a, in the nervous system. Since neurons in cranial sensory ganglia and dorsal root ganglia transiently express Ngn1, NeuroD and Brn3a during embryonic development, we hypothesized that Wnt proteins could instructively promote a sensory neuronal fate from mesencymal stem cells (MSCs) directed to differentiate into neurons. Consistent with our hypothesis, Wnt1 induced expression of sensory neuron markers including Ngn1, NeuroD and Brn3a, as well as glutamatergic markers in neurally-induced MSCs in vitro and promoted engraftment of transplanted MSCs in the inner ear bearing selective loss of sensory neurons in vivo. Given the consensus function of T cell leukemia 3 (Tlx3), as a glutamatergic selector gene, we postulated that the effects of canonical Wnt signaling on sensory neuron and glutamatergic marker gene expression in MSCs may be mediated by Tlx3. We first confirmed that Wnt1 indeed up-regulates Tlx3 expression, which can be suppressed by canonical Wnt inhibitors. Next, our chromatin immunoprecipitation assays revealed that T-cell factor 3/4 (TCF3/4), Wnt-activated DNA binding proteins, interact with a regulatory region of Tlx3 in MSCs after neural induction. Furthermore, we demonstrated that forced expression of Tlx3 in MSCs induced sensory and glutamatergic neuron markers after neural induction. Together, these results identify Tlx3 as a novel target for canonical Wnt signaling that confers somatic stem cells with a sensory neuron phenotype upon neural induction.
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