FGF signaling refines Wnt gradients to regulate the patterning of taste papillae

被引:22
作者
Prochazkova, Michaela [1 ,2 ,3 ,4 ]
Hakkinen, Teemu J. [5 ]
Prochazka, Jan [1 ,2 ,3 ,4 ]
Spoutil, Frantisek [3 ,4 ]
Jheon, Andrew H. [1 ,2 ]
Ahn, Youngwook [6 ]
Krumlauf, Robb [6 ,7 ]
Jernvall, Jukka [5 ]
Klein, Ophir D. [1 ,2 ,8 ,9 ]
机构
[1] Univ Calif San Francisco, Dept Orofacial Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Program Craniofacial Biol, San Francisco, CA 94143 USA
[3] Inst Mol Genet CAS, Czech Ctr Phenogen, Vvi, Prumyslova 595, Vestec 25242, Czech Republic
[4] Div BIOCEV, Lab Transgen Models Dis, Prumyslova 595, Vestec 25242, Czech Republic
[5] Univ Helsinki, Inst Biotechnol, Dev Biol Program, POB 56, FIN-00014 Helsinki, Finland
[6] Stowers Inst Med Res, Kansas City, MO 64110 USA
[7] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA
[8] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[9] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
来源
DEVELOPMENT | 2017年 / 144卷 / 12期
基金
芬兰科学院;
关键词
FGF; Wnt; Tongue; Taste papilla; FUNGIFORM PAPILLA; TOOTH; WISE; MOUSE; SHH; TONGUE; MAINTENANCE; EPITHELIUM; PLACODES; MAMMARY;
D O I
10.1242/dev.148080
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
The patterning of repeated structures is a major theme in developmental biology, and the inter-relationship between spacing and size of such structures is an unresolved issue. Fungiform papillae are repeated epithelial structures that house taste buds on the anterior tongue. Here, we report that FGF signaling is a crucial regulator of fungiform papillae development. We found that mesenchymal FGF10 controls the size of the papillary area, while overall patterning remains unchanged. Our results show that FGF signaling negatively affects the extent of canonical Wnt signaling, which is the main activation pathway during fungiform papillae development; however, this effect does not occur at the level of gene transcription. Rather, our experimental data, together with computational modeling, indicate that FGF10 modulates the range of Wnt effects, likely via induction of Sostdc1 expression. We suggest that modification of the reach of Wnt signaling could be due to local changes in morphogen diffusion, representing a novel mechanism in this tissue context, and we propose that this phenomenon might be involved in a broader array of mammalian developmental processes.
引用
收藏
页码:2212 / 2221
页数:10
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