| Literature DB >> 25959824 |
Janos Tözser1, Ryan Earwood2, Akiko Kato2, Jacob Brown2, Koichi Tanaka2, Ruth Didier2, Timothy L Megraw2, Martin Blum3, Yoichi Kato4.
Abstract
The cilium is a small cellular organelle with motility- and/or sensory-related functions that plays a crucial role during developmental and homeostatic processes. Although many molecules or signal transduction pathways that control cilia assembly have been reported, the mechanisms of ciliary length control have remained enigmatic. Here, we report that Smad2-dependent transforming growth factor β (TGF-β) signaling impacts the length of motile cilia at the Xenopus left-right (LR) organizer, the gastrocoel roof plate (GRP), as well as at the neural tube and the epidermis. Blocking TGF-β signaling resulted in the absence of the transition zone protein B9D1/MSKR-1 from cilia in multi-ciliated cells (MCCs) of the epidermis. Interestingly, this TGF-β activity is not mediated by Mcidas, Foxj1, and RFX2, the known major regulators of ciliogenesis. These data indicate that TGF-β signaling is crucial for the function of the transition zone, which in turn may affect the regulation of cilia length.Entities:
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Year: 2015 PMID: 25959824 PMCID: PMC4439334 DOI: 10.1016/j.celrep.2015.04.025
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423