Purified Wnt-5a increases differentiation of midbrain dopaminergic cells and dishevelled phosphorylation

被引:102
作者
Schulte, G [1 ]
Bryja, V [1 ]
Rawal, N [1 ]
Castelo-Branco, G [1 ]
Sousa, KM [1 ]
Arenas, E [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, Mol Neurobiol Lab, S-17177 Stockholm, Sweden
关键词
beta-catenin; dopaminergic neurones; proliferation; SN4741; Wnt-3a; Wnt signalling;
D O I
10.1111/j.1471-4159.2004.03022.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Wnt family of lipoproteins regulates several aspects of the development of the nervous system. Recently, we reported that Wnt-3a enhances the proliferation of midbrain dopaminergic precursors and that Wnt-5a promotes their differentiation into dopaminergic neurones. Here we report the purification of hemagglutinin-tagged Wnt-5a using a three-step purification method similar to that previously described for Wnt-3a. Haemagglutinin-tagged Wnt-5a was biologically active and induced the differentiation of immature primary midbrain precursors into tyrosine hydroxylase-positive dopaminergic neurones. Using a substantia nigra-derived dopaminergic cell line (SN4741), we found that Wnt-5a, unlike Wnt-3a, did not promote beta-catenin phosphorylation or stabilization. However, both Wnt-5a and Wnt-3a activated dishevelled, as assessed by a phosphorylation-dependent mobility shift. Moreover, the activity of Wnt-5a on dishevelled was blocked by pre-treatment with acyl protein thioesterase-1, indicating that palmitoylation of Wnt-5a is necessary for its function. Thus, our results suggest that Wnt-3a and Wnt-5a, respectively, activate canonical and non-canonical Wnt signalling pathways in ventral midbrain dopaminergic cells. Furthermore, we identify dishevelled as a key player in transducing both Wnt canonical and non-canonical signals in dopaminergic cells.
引用
收藏
页码:1550 / 1553
页数:4
相关论文
共 19 条
[1]   Differential regulation of midbrain dopaminergic neuron development by Wnt-1, Wnt-3a, and Wnt-5a [J].
Castelo-Branco, GA ;
Wagner, J ;
Rodriguez, FJ ;
Kele, J ;
Sousa, K ;
Rawal, N ;
Pasolli, HA ;
Fuchs, E ;
Kitajewski, J ;
Arenas, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12747-12752
[2]   Dishevelled 2 recruits β-arrestin 2 to mediate Wnt5A-stimulated endocytosis of Frizzled 4 [J].
Chen, W ;
ten Berge, D ;
Brown, J ;
Ahn, S ;
Hu, LA ;
Miller, WE ;
Caron, MG ;
Barak, LS ;
Nusse, R ;
Lefkowitz, RJ .
SCIENCE, 2003, 301 (5638) :1391-1394
[3]   Casein kinase Iε modulates the signaling specificities of dishevelled [J].
Cong, F ;
Schweizer, L ;
Varmus, H .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (05) :2000-2011
[4]   Wnt proteins induce dishevelled phosphorylation via an LRP5/6-Independent mechanism, irrespective of their ability to stabilize β-catenin [J].
González-Sancho, JM ;
Brennan, KR ;
Castelo-Soccio, LA ;
Brown, AMC .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (11) :4757-4768
[5]   Specificity of WNT-receptor interactions [J].
Hsieh, JC .
FRONTIERS IN BIOSCIENCE, 2004, 9 :1333-1338
[6]   The Wnt signalling pathway [J].
Huelsken, J ;
Behrens, J .
JOURNAL OF CELL SCIENCE, 2002, 115 (21) :3977-3978
[7]   The TAK1-NLK mitogen-activated protein kinase cascade functions in the Wnt-5a/Ca2+ pathway to antagonize Wnt/β-catenin signaling [J].
Ishitani, T ;
Kishida, S ;
Hyodo-Miura, J ;
Ueno, N ;
Yasuda, J ;
Waterman, M ;
Shibuya, H ;
Moon, RT ;
Ninomiya-Tsuji, J ;
Matsumoto, K .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :131-139
[8]  
Jansson M, 2001, J CELL SCI, V114, P2043
[9]   Ca2+/calmodulin-dependent protein kinase II is stimulated by Wnt and frizzled homologs and promotes ventral cell fates in Xenopus [J].
Kühl, M ;
Sheldahl, LC ;
Malbon, CC ;
Moon, RT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12701-12711
[10]   Frizzleds: New members of the superfamily of G-protein-coupled receptors [J].
Malbon, CC .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :1048-1058