Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

Persistence of Cajal-Retzius cells in the postnatal hippocampus is required for development of dendritic spines of CA1 pyramidal cells

Ingvild Lynneberg Glærum, View ORCID ProfileKeagan Dunville, View ORCID ProfileNicola Pietro Montaldo, Hinako Kirikae, View ORCID ProfileMaximiliano Jose Nigro, View ORCID ProfilePål Sætrom, View ORCID ProfileBarbara van Loon, View ORCID ProfileGiulia Quattrocolo
doi: https://doi.org/10.1101/2022.05.09.491146
Ingvild Lynneberg Glærum
1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
2Mohn Research Center for the Brain, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Keagan Dunville
1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Keagan Dunville
Nicola Pietro Montaldo
3Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, 7491, Norway
4Department of Microbiology, Oslo University Hospital and University of Oslo, Oslo, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Nicola Pietro Montaldo
Hinako Kirikae
1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
5Department of Organ Anatomy, Graduate School of Medicine, Tohoku University
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Maximiliano Jose Nigro
1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Maximiliano Jose Nigro
Pål Sætrom
3Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Pål Sætrom
Barbara van Loon
3Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Barbara van Loon
Giulia Quattrocolo
1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
2Mohn Research Center for the Brain, Norwegian University of Science and Technology (NTNU), Trondheim 7491, Norway
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Giulia Quattrocolo
  • For correspondence: giulia.quattrocolo@ntnu.no
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Preview PDF
Loading

Summary

Cajal-Retzius (CR) cells are a transient type of neuron that populate the postnatal hippocampus. The role of transient cell types and circuits have been vastly addressed in neocortical regions, but poorly studied in the hippocampus. To understand how CR cells’ persistence influences the maturation of hippocampal circuits, we specifically ablated CR cells from the postnatal hippocampus. Our results highlighted layer-specific effects on dendritic spines and synaptic-related genes and revealed a critical role of CR cells in the establishment of the hippocampal network.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
Back to top
PreviousNext
Posted May 10, 2022.
Download PDF
Email

Thank you for your interest in spreading the word about bioRxiv.

NOTE: Your email address is requested solely to identify you as the sender of this article.

Enter multiple addresses on separate lines or separate them with commas.
Persistence of Cajal-Retzius cells in the postnatal hippocampus is required for development of dendritic spines of CA1 pyramidal cells
(Your Name) has forwarded a page to you from bioRxiv
(Your Name) thought you would like to see this page from the bioRxiv website.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Persistence of Cajal-Retzius cells in the postnatal hippocampus is required for development of dendritic spines of CA1 pyramidal cells
Ingvild Lynneberg Glærum, Keagan Dunville, Nicola Pietro Montaldo, Hinako Kirikae, Maximiliano Jose Nigro, Pål Sætrom, Barbara van Loon, Giulia Quattrocolo
bioRxiv 2022.05.09.491146; doi: https://doi.org/10.1101/2022.05.09.491146
Reddit logo Twitter logo Facebook logo LinkedIn logo Mendeley logo
Citation Tools
Persistence of Cajal-Retzius cells in the postnatal hippocampus is required for development of dendritic spines of CA1 pyramidal cells
Ingvild Lynneberg Glærum, Keagan Dunville, Nicola Pietro Montaldo, Hinako Kirikae, Maximiliano Jose Nigro, Pål Sætrom, Barbara van Loon, Giulia Quattrocolo
bioRxiv 2022.05.09.491146; doi: https://doi.org/10.1101/2022.05.09.491146

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Subject Area

  • Neuroscience
Subject Areas
All Articles
  • Animal Behavior and Cognition (4225)
  • Biochemistry (9101)
  • Bioengineering (6750)
  • Bioinformatics (23941)
  • Biophysics (12087)
  • Cancer Biology (9493)
  • Cell Biology (13738)
  • Clinical Trials (138)
  • Developmental Biology (7614)
  • Ecology (11659)
  • Epidemiology (2066)
  • Evolutionary Biology (15477)
  • Genetics (10616)
  • Genomics (14293)
  • Immunology (9460)
  • Microbiology (22774)
  • Molecular Biology (9069)
  • Neuroscience (48851)
  • Paleontology (354)
  • Pathology (1479)
  • Pharmacology and Toxicology (2564)
  • Physiology (3822)
  • Plant Biology (8308)
  • Scientific Communication and Education (1467)
  • Synthetic Biology (2289)
  • Systems Biology (6171)
  • Zoology (1297)