Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis

Ciliogenesis is a complex process requiring hundreds of molecules, although few secreted proteins have been implicated. Here, the authors show that the secreted metalloproteases ADAMTS9 and ADAMTS20 intracellularly regulate ciliogenesis from unique periciliary vesicles with proteolytic activity.

Guardado en:
Detalles Bibliográficos
Autores principales: Sumeda Nandadasa, Caroline M. Kraft, Lauren W. Wang, Anna O’Donnell, Rushabh Patel, Heon Yung Gee, Kay Grobe, Timothy C. Cox, Friedhelm Hildebrandt, Suneel S. Apte
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
Materias:
Q
Acceso en línea:https://doaj.org/article/ab5baac1ec5848ec9b9f690a16ccfcb8
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ab5baac1ec5848ec9b9f690a16ccfcb8
record_format dspace
spelling oai:doaj.org-article:ab5baac1ec5848ec9b9f690a16ccfcb82021-12-02T16:57:06ZSecreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis10.1038/s41467-019-08520-72041-1723https://doaj.org/article/ab5baac1ec5848ec9b9f690a16ccfcb82019-02-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-08520-7https://doaj.org/toc/2041-1723Ciliogenesis is a complex process requiring hundreds of molecules, although few secreted proteins have been implicated. Here, the authors show that the secreted metalloproteases ADAMTS9 and ADAMTS20 intracellularly regulate ciliogenesis from unique periciliary vesicles with proteolytic activity.Sumeda NandadasaCaroline M. KraftLauren W. WangAnna O’DonnellRushabh PatelHeon Yung GeeKay GrobeTimothy C. CoxFriedhelm HildebrandtSuneel S. ApteNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-19 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Sumeda Nandadasa
Caroline M. Kraft
Lauren W. Wang
Anna O’Donnell
Rushabh Patel
Heon Yung Gee
Kay Grobe
Timothy C. Cox
Friedhelm Hildebrandt
Suneel S. Apte
Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
description Ciliogenesis is a complex process requiring hundreds of molecules, although few secreted proteins have been implicated. Here, the authors show that the secreted metalloproteases ADAMTS9 and ADAMTS20 intracellularly regulate ciliogenesis from unique periciliary vesicles with proteolytic activity.
format article
author Sumeda Nandadasa
Caroline M. Kraft
Lauren W. Wang
Anna O’Donnell
Rushabh Patel
Heon Yung Gee
Kay Grobe
Timothy C. Cox
Friedhelm Hildebrandt
Suneel S. Apte
author_facet Sumeda Nandadasa
Caroline M. Kraft
Lauren W. Wang
Anna O’Donnell
Rushabh Patel
Heon Yung Gee
Kay Grobe
Timothy C. Cox
Friedhelm Hildebrandt
Suneel S. Apte
author_sort Sumeda Nandadasa
title Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
title_short Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
title_full Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
title_fullStr Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
title_full_unstemmed Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
title_sort secreted metalloproteases adamts9 and adamts20 have a non-canonical role in ciliary vesicle growth during ciliogenesis
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/ab5baac1ec5848ec9b9f690a16ccfcb8
work_keys_str_mv AT sumedanandadasa secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT carolinemkraft secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT laurenwwang secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT annaodonnell secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT rushabhpatel secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT heonyunggee secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT kaygrobe secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT timothyccox secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT friedhelmhildebrandt secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
AT suneelsapte secretedmetalloproteasesadamts9andadamts20haveanoncanonicalroleinciliaryvesiclegrowthduringciliogenesis
_version_ 1718382641559896064