Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures

Summary: Secretory pathways within dendrites of neurons have been proposed for local transport of newly synthesized proteins. However, little is known about the dynamics of the local secretory system and whether the organelles are transient or stable structures. Here, we quantify the spatial and dyn...

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Main Authors: Jingqi Wang, Maciej Daniszewski, Marlene M. Hao, Damián Hernández, Alice Pébay, Paul A. Gleeson, Lou Fourriere
Format: Article
Language:English
Published: Elsevier 2023-07-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124723007209
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author Jingqi Wang
Maciej Daniszewski
Marlene M. Hao
Damián Hernández
Alice Pébay
Paul A. Gleeson
Lou Fourriere
author_facet Jingqi Wang
Maciej Daniszewski
Marlene M. Hao
Damián Hernández
Alice Pébay
Paul A. Gleeson
Lou Fourriere
author_sort Jingqi Wang
collection DOAJ
description Summary: Secretory pathways within dendrites of neurons have been proposed for local transport of newly synthesized proteins. However, little is known about the dynamics of the local secretory system and whether the organelles are transient or stable structures. Here, we quantify the spatial and dynamic behavior of dendritic Golgi and endosomes during differentiation of human neurons generated from induced pluripotent stem cells (iPSCs). In early neuronal development, before and during migration, the entire Golgi apparatus transiently translocates from the soma into dendrites. In mature neurons, dynamic Golgi elements, containing cis and trans cisternae, are transported from the soma along dendrites, in an actin-dependent process. Dendritic Golgi outposts are dynamic and display bidirectional movement. Similar structures were observed in cerebral organoids. Using the retention using selective hooks (RUSH) system, Golgi resident proteins are transported efficiently into Golgi outposts from the endoplasmic reticulum. This study reveals dynamic, functional Golgi structures in dendrites and a spatial map for investigating dendrite trafficking in human neurons.
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spelling doaj.art-7c5800b8066d4d5a9238cde3018867d72023-07-02T04:16:37ZengElsevierCell Reports2211-12472023-07-01427112709Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structuresJingqi Wang0Maciej Daniszewski1Marlene M. Hao2Damián Hernández3Alice Pébay4Paul A. Gleeson5Lou Fourriere6The Department of Biochemistry and Pharmacology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC 3010, AustraliaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC 3010, Australia; Department of Surgery, Royal Melbourne Hospital, The University of Melbourne, Parkville, VIC 3010, AustraliaThe Department of Biochemistry and Pharmacology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia; Corresponding authorThe Department of Biochemistry and Pharmacology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia; Corresponding authorSummary: Secretory pathways within dendrites of neurons have been proposed for local transport of newly synthesized proteins. However, little is known about the dynamics of the local secretory system and whether the organelles are transient or stable structures. Here, we quantify the spatial and dynamic behavior of dendritic Golgi and endosomes during differentiation of human neurons generated from induced pluripotent stem cells (iPSCs). In early neuronal development, before and during migration, the entire Golgi apparatus transiently translocates from the soma into dendrites. In mature neurons, dynamic Golgi elements, containing cis and trans cisternae, are transported from the soma along dendrites, in an actin-dependent process. Dendritic Golgi outposts are dynamic and display bidirectional movement. Similar structures were observed in cerebral organoids. Using the retention using selective hooks (RUSH) system, Golgi resident proteins are transported efficiently into Golgi outposts from the endoplasmic reticulum. This study reveals dynamic, functional Golgi structures in dendrites and a spatial map for investigating dendrite trafficking in human neurons.http://www.sciencedirect.com/science/article/pii/S2211124723007209CP: Cell biologyCP: Neuroscience
spellingShingle Jingqi Wang
Maciej Daniszewski
Marlene M. Hao
Damián Hernández
Alice Pébay
Paul A. Gleeson
Lou Fourriere
Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
Cell Reports
CP: Cell biology
CP: Neuroscience
title Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
title_full Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
title_fullStr Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
title_full_unstemmed Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
title_short Organelle mapping in dendrites of human iPSC-derived neurons reveals dynamic functional dendritic Golgi structures
title_sort organelle mapping in dendrites of human ipsc derived neurons reveals dynamic functional dendritic golgi structures
topic CP: Cell biology
CP: Neuroscience
url http://www.sciencedirect.com/science/article/pii/S2211124723007209
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