Roles of Primary Cilia in the Developing Brain

Essential to development, primary cilia are microtubule-based cellular organelles that protrude from the surface of cells. Acting as cellular antenna, primary cilia play central roles in transducing or regulating several signaling pathways, including Sonic hedgehog (Shh) and Wnt signaling. Defects i...

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Main Authors: Sang Min Park, Hee Jin Jang, Jeong Ho Lee
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-05-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Wnt
Online Access:https://www.frontiersin.org/article/10.3389/fncel.2019.00218/full
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spelling doaj-708b34e2192b47bd923411fb17f1c0b02020-11-25T02:16:48ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022019-05-011310.3389/fncel.2019.00218448640Roles of Primary Cilia in the Developing BrainSang Min Park0Hee Jin Jang1Jeong Ho Lee2Jeong Ho Lee3Biomedical Science and Engineering Interdisciplinary Program, Korea Advanced Institute of Science and Technology, Daejeon, South KoreaBiomedical Science and Engineering Interdisciplinary Program, Korea Advanced Institute of Science and Technology, Daejeon, South KoreaBiomedical Science and Engineering Interdisciplinary Program, Korea Advanced Institute of Science and Technology, Daejeon, South KoreaGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South KoreaEssential to development, primary cilia are microtubule-based cellular organelles that protrude from the surface of cells. Acting as cellular antenna, primary cilia play central roles in transducing or regulating several signaling pathways, including Sonic hedgehog (Shh) and Wnt signaling. Defects in primary cilia contribute to a group of syndromic disorders known as “ciliopathies” and can adversely affect development of the brain and other essential organs, including the kidneys, eyes, and liver. The molecular mechanisms of how defective primary cilia contribute to neurological defects, however, remain poorly understood. In this mini review, we summarize recent advances in understanding of the interactions between primary cilia and signaling pathways essential to cellular homeostasis and brain development.https://www.frontiersin.org/article/10.3389/fncel.2019.00218/fullprimary ciliaWntMTORautophagyciliopathyFMCD
collection DOAJ
language English
format Article
sources DOAJ
author Sang Min Park
Hee Jin Jang
Jeong Ho Lee
Jeong Ho Lee
spellingShingle Sang Min Park
Hee Jin Jang
Jeong Ho Lee
Jeong Ho Lee
Roles of Primary Cilia in the Developing Brain
Frontiers in Cellular Neuroscience
primary cilia
Wnt
MTOR
autophagy
ciliopathy
FMCD
author_facet Sang Min Park
Hee Jin Jang
Jeong Ho Lee
Jeong Ho Lee
author_sort Sang Min Park
title Roles of Primary Cilia in the Developing Brain
title_short Roles of Primary Cilia in the Developing Brain
title_full Roles of Primary Cilia in the Developing Brain
title_fullStr Roles of Primary Cilia in the Developing Brain
title_full_unstemmed Roles of Primary Cilia in the Developing Brain
title_sort roles of primary cilia in the developing brain
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2019-05-01
description Essential to development, primary cilia are microtubule-based cellular organelles that protrude from the surface of cells. Acting as cellular antenna, primary cilia play central roles in transducing or regulating several signaling pathways, including Sonic hedgehog (Shh) and Wnt signaling. Defects in primary cilia contribute to a group of syndromic disorders known as “ciliopathies” and can adversely affect development of the brain and other essential organs, including the kidneys, eyes, and liver. The molecular mechanisms of how defective primary cilia contribute to neurological defects, however, remain poorly understood. In this mini review, we summarize recent advances in understanding of the interactions between primary cilia and signaling pathways essential to cellular homeostasis and brain development.
topic primary cilia
Wnt
MTOR
autophagy
ciliopathy
FMCD
url https://www.frontiersin.org/article/10.3389/fncel.2019.00218/full
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