MKP3 mediates the cellular response to FGF8 signalling in the vertebrate limb

Yasuhiko Kawakami, Joaquín Rodríguez-León, Christopher M. Koth, Dirk Büscher, Tohru Itoh, Ángel Raya, Jennifer K. Ng, Concepción Rodríguez Esteban, Shigeru Takahashi, Domingos Henrique, May Fun Schwarz, Hiroshi Asahara, Juan Carlos Izpisúa Belmonte

Research output: Contribution to journalReview articlepeer-review

215 Scopus citations

Abstract

The mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) and phosphatidylinositol-3-OH kinase (PI(3)K)/Akt pathways are involved in the regulatory mechanisms of several cellular processes including proliferation, differentiation and apoptosis. Here we show that during chick, mouse and zebrafish limb/fin development, a known MAPK/ERK regulator, Mkp3, is induced in the mesenchyme by fibroblast growth factor 8 (FGF8) signalling, through the PI(3)K/Akt pathway. This correlates with a high level of phosphorylated ERK in the apical ectodermal ridge (AER), where Mkp3 expression is excluded. Conversely, phosphorylated Akt is detected only in the mesenchyme. Constitutively active Mek1, as well as the downregulation of Mkp3 by small interfering RNA (siRNA), induced apoptosis in the mesenchyme. This suggests that MKP3 has a key role in mediating the proliferative, anti-apoptotic signalling of AER-derived FGF8.

Original languageEnglish (US)
Pages (from-to)513-519
Number of pages7
JournalNature Cell Biology
Volume5
Issue number6
DOIs
StatePublished - Jun 1 2003

Bibliographical note

Funding Information:
We thank G. Martin for providing limb-specific Fgf4;Fgf8 double-knockout mouse embryos, C. Nuesslein Volhard for the mutant zebrafish dackel, M. Aoki and P. Vogt for the constitutively active Akt construct, T. Jessell for the chick Pea3 and Er81 clones, E. Nishida for the constitutively active Mek1 clone, I. Dubova for his expertise and help with zebrafish, G. Sternik for his assistance with the microscopic analyses, and M. Tsuda for assistance with experiments. J.R.L. is supported by a fellowship from the Fundação Calouste Gulbenkian. T.I. is supported by a JSPS Postdoctoral Fellowship for Research Abroad, Japan. C.M.K. is partly supported by a postdoctoral fellowship from the Canadian Institutes of Health Research, J.K.N. is supported by an NIH training grant, and A.R. is partly supported by a postdoctoral fellowship from the Ministerio de Educación, Cultura y Deporte, Spain. H.A. is supported by the Arthritis Foundation and the Japan Science and Technology Cooperation. This work was supported by grants from BioCell, Fundacao Calouste Gulbenkian e Fundacao para Ciencia e Technologia, the Arthritis Foundation, the G. Harold and Leila Y. Mathers Charitable Foundation, the National Science Foundation, and the National Institutes of Health.

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