- Oral presentation
- Open Access
Transforming growth factor beta (TGFβ) signaling is regulated at the pocket region of primary cilia
© Christensen et al; licensee BioMed Central Ltd. 2012
- Published: 16 November 2012
- Transform Growth Factor Beta
- Human Embryonic Stem Cell
- Mouse Embryonic Fibroblast
- Primary Cilium
- Smad Signaling
TGFβ signaling extensively cross-talks with Hh, Wnt and RTK signaling to control cell proliferation, migration and differentiation, and when aberrantly regulated leads to developmental defects and cancer. TGFβ signaling is activated through the internalization of TGFβ receptors via clathrin-dependent endocytosis (CDE), at which the receptor activates Smad transcription factors. Here we investigated the relationship between TGFβ signaling and primary cilia in fibroblasts and in EC and human embryonic stem cells during their differentiation into cardiomyocytes and neurons using transcriptomics, imaging and molecular biology tools. During cardiomyocyte differentiation, expression of TGFβ receptors and Smad proteins were up-regulated and targeted to the pocket region of primary cilia, at which the receptor colocalized with clathrin-coated pits and vesicles to activate Smad2/3. This activation was blocked by receptor antagonists or by Ift20 knockdown. In contrast, neuronal differentiation was associated with a loss of ciliary TGFβ signaling. In mouse embryonic fibroblasts (MEFs) and human foreskin fibroblasts (hFFs), TGFβ stimulation increased the targeting of TGFβ receptors to the ciliary pocket region followed by activation of Smad signaling to promote cell cycle entry. In Tg737orpk MEFs there was a major reduction in TGFβ-induced Smad2/3 phosphorylation, and this was associated with reduced activity of clathrin-dependent endocytosis at stumpy primary cilia. Similarly, inhibition of CDE blocked activation of Smad2/3 at the ciliary pocket region in hFFs. Our results suggest that the ciliary pocket region functions as a unique site for regulation of TGFβ signaling and potentially in cross-talking with other signaling pathways during development and in tissue homeostasis.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.