SFRP1 and SFRP2 Dose-Dependently Regulate Midbrain Dopamine Neuron Development In Vivo and in Embryonic Stem Cells

被引:52
|
作者
Kele, Julianna [1 ]
Andersson, Emma R. [1 ]
Villaescusa, J. Carlos [1 ]
Cajanek, Lukas [1 ]
Parish, Clare L. [2 ,3 ]
Bonilla, Sonia [1 ]
Toledo, Enrique M. [1 ]
Bryja, Vitezslav [1 ]
Rubin, Jeffrey S. [4 ]
Shimono, Akihiko [5 ]
Arenas, Ernest [1 ]
机构
[1] Karolinska Inst, Lab Mol Neurobiol Med Biochem & Biophys, S-17177 Stockholm, Sweden
[2] Univ Melbourne, Florey Neurosci Inst, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Ctr Neurosci, Parkville, Vic 3052, Australia
[4] NCI CCR LCMB, MSC 4255, Bethesda, MD USA
[5] Natl Univ Singapore, Ctr Life Sci 02 07, Canc Sci Inst Singapore, Singapore, Singapore
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会; 瑞典研究理事会;
关键词
Embryonic stem cells; Neural differentiation; Developmental biology; Parkinson's disease; FRIZZLED-RELATED PROTEIN-1; DISHEVELLED PHOSPHORYLATION; INCREASES DIFFERENTIATION; INT-1; PROTOONCOGENE; PARKINSONS-DISEASE; SPEMANN ORGANIZER; WNT/BETA-CATENIN; WNT ANTAGONIST; NERVOUS-SYSTEM; MOUSE;
D O I
10.1002/stem.1049
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Secreted Frizzled related proteins (sFRPs) are a family of proteins that modulate Wnt signaling, which in turn regulates multiple aspects of ventral midbrain (VM) and dopamine (DA) neuron development. However, it is not known which Wnt signaling branch and what aspects of midbrain DA neuron development are regulated by sFRPs. Here, we show that sFRP1 and sFRP2 activate the Wnt/planar-cell-polarity/Rac1 pathway in DA cells. In the developing VM, sFRP1 and sFRP2 are expressed at low levels, and sFRP1-/- or sFRP2-/- mice had no detectable phenotype. However, compound sFRP1-/-;sFRP2-/- mutants revealed a Wnt/PCP phenotype similar to that previously described for Wnt5a-/- mice. This included an anteroposterior shortening of the VM, a lateral expansion of the Shh domain and DA lineage markers (Lmx1a and Th), as well as an accumulation of Nurr1+ precursors in the VM. In vitro experiments showed that, while very high concentrations of SFRP1 had a negative effect on cell survival, low/medium concentrations of sFRP1 or sFRP2 promoted the DA differentiation of progenitors derived from primary VM cultures or mouse embryonic stem cells (ESCs), mimicking the effects of Wnt5a. We thus conclude that the main function of sFRP1 and sFRP2 is to enhance Wnt/PCP signaling in DA cells and to regulate Wnt/PCP-dependent functions in midbrain development. Moreover, we suggest that lowmedium concentrations of sFRPs may be used to enhance the DA differentiation of ESCs and improve their therapeutic application. STEM CELLS 2012;30:865875
引用
收藏
页码:865 / 875
页数:11
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