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Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport

Cilia are microtubule-based organelles that mediate signal transduction in a variety of tissues. Despite their importance, the signaling cascades that regulate cilia formation remain incompletely understood. Here we report that prostaglandin signaling affects ciliogenesis by regulating anterograde i...

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Autores principales: Jin, Daqing, Ni, Terri T., Sun, Jianjian, Wan, Haiyan, Amack, Jeffrey D., Yu, Guangju, Fleming, Jonathan, Chiang, Chin, Li, Wenyan, Papierniak, Anna, Cheepala, Satish, Conseil, Gwenaëlle, Cole, Susan P.C., Zhou, Bin, Drummond, Iain A., Schuetz, John D., Malicki, Jarema, Zhong, Tao P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154319/
https://www.ncbi.nlm.nih.gov/pubmed/25173977
http://dx.doi.org/10.1038/ncb3029
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author Jin, Daqing
Ni, Terri T.
Sun, Jianjian
Wan, Haiyan
Amack, Jeffrey D.
Yu, Guangju
Fleming, Jonathan
Chiang, Chin
Li, Wenyan
Papierniak, Anna
Cheepala, Satish
Conseil, Gwenaëlle
Cole, Susan P.C.
Zhou, Bin
Drummond, Iain A.
Schuetz, John D.
Malicki, Jarema
Zhong, Tao P.
author_facet Jin, Daqing
Ni, Terri T.
Sun, Jianjian
Wan, Haiyan
Amack, Jeffrey D.
Yu, Guangju
Fleming, Jonathan
Chiang, Chin
Li, Wenyan
Papierniak, Anna
Cheepala, Satish
Conseil, Gwenaëlle
Cole, Susan P.C.
Zhou, Bin
Drummond, Iain A.
Schuetz, John D.
Malicki, Jarema
Zhong, Tao P.
author_sort Jin, Daqing
collection PubMed
description Cilia are microtubule-based organelles that mediate signal transduction in a variety of tissues. Despite their importance, the signaling cascades that regulate cilia formation remain incompletely understood. Here we report that prostaglandin signaling affects ciliogenesis by regulating anterograde intraflagellar transport (IFT). Zebrafish leakytail (lkt) mutants display ciliogenesis defects, and lkt locus encodes an ATP-binding cassette transporter (ABCC4). We show that Lkt/ABCC4 localizes to the cell membrane and exports prostaglandin E(2) (PGE(2)), a function that is abrogated by the Lkt/ABCC4(T804M) mutant. PGE(2) synthesis enzyme Cyclooxygenase-1 and its receptor, EP4, which localizes to the cilium and activates cAMP-mediated signaling cascade, are required for cilia formation and elongation. Importantly, PGE(2) signaling increases anterograde but not retrograde velocity of IFT and promotes ciliogenesis in mammalian cells. These findings lead us to propose that Lkt/ABCC4-mediated PGE(2) signaling acts through a ciliary G-protein-coupled receptor, EP4, to upregulate cAMP synthesis and increase anterograde IFT, thereby promoting ciliogenesis.
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spelling pubmed-41543192015-03-01 Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport Jin, Daqing Ni, Terri T. Sun, Jianjian Wan, Haiyan Amack, Jeffrey D. Yu, Guangju Fleming, Jonathan Chiang, Chin Li, Wenyan Papierniak, Anna Cheepala, Satish Conseil, Gwenaëlle Cole, Susan P.C. Zhou, Bin Drummond, Iain A. Schuetz, John D. Malicki, Jarema Zhong, Tao P. Nat Cell Biol Article Cilia are microtubule-based organelles that mediate signal transduction in a variety of tissues. Despite their importance, the signaling cascades that regulate cilia formation remain incompletely understood. Here we report that prostaglandin signaling affects ciliogenesis by regulating anterograde intraflagellar transport (IFT). Zebrafish leakytail (lkt) mutants display ciliogenesis defects, and lkt locus encodes an ATP-binding cassette transporter (ABCC4). We show that Lkt/ABCC4 localizes to the cell membrane and exports prostaglandin E(2) (PGE(2)), a function that is abrogated by the Lkt/ABCC4(T804M) mutant. PGE(2) synthesis enzyme Cyclooxygenase-1 and its receptor, EP4, which localizes to the cilium and activates cAMP-mediated signaling cascade, are required for cilia formation and elongation. Importantly, PGE(2) signaling increases anterograde but not retrograde velocity of IFT and promotes ciliogenesis in mammalian cells. These findings lead us to propose that Lkt/ABCC4-mediated PGE(2) signaling acts through a ciliary G-protein-coupled receptor, EP4, to upregulate cAMP synthesis and increase anterograde IFT, thereby promoting ciliogenesis. 2014-08-31 2014-09 /pmc/articles/PMC4154319/ /pubmed/25173977 http://dx.doi.org/10.1038/ncb3029 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Jin, Daqing
Ni, Terri T.
Sun, Jianjian
Wan, Haiyan
Amack, Jeffrey D.
Yu, Guangju
Fleming, Jonathan
Chiang, Chin
Li, Wenyan
Papierniak, Anna
Cheepala, Satish
Conseil, Gwenaëlle
Cole, Susan P.C.
Zhou, Bin
Drummond, Iain A.
Schuetz, John D.
Malicki, Jarema
Zhong, Tao P.
Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title_full Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title_fullStr Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title_full_unstemmed Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title_short Prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
title_sort prostaglandin signaling regulates ciliogenesis by modulating intraflagellar transport
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154319/
https://www.ncbi.nlm.nih.gov/pubmed/25173977
http://dx.doi.org/10.1038/ncb3029
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