TY - JOUR
T1 - Primary cilia are required for the persistence of memory and stabilization of perineuronal nets
AU - Jovasevic, Vladimir
AU - Zhang, Hui
AU - Sananbenesi, Farahnaz
AU - Guedea, Anita L.
AU - Soman, Kizhake V.
AU - Wiktorowicz, John E.
AU - Fischer, Andre
AU - Radulovic, Jelena
N1 - Funding Information:
We thank Dr. Paul DeCaen (Northwestern University) for providing Arl13B-GFP P1 mice for our in vitro studies, and Mr. Daniel Abdella for editing the manuscript and for assistance with the manuscript preparation. This work was funded by NIMH grant MH078064 to J.R.
Publisher Copyright:
© 2021 The Authors
PY - 2021/6/25
Y1 - 2021/6/25
N2 - It is well established that the formation of episodic memories requires multiple hippocampal mechanisms operating on different time scales. Early mechanisms of memory formation (synaptic consolidation) have been extensively characterized. However, delayed mechanisms, which maintain hippocampal activity as memories stabilize in cortical circuits, are not well understood. Here we demonstrate that contrary to the transient expression of early- and delayed-response genes, the expression of cytoskeleton- and extracellular matrix-associated genes remains dynamic even at remote time points. The most profound expression changes clustered around primary cilium-associated and collagen genes. These genes most likely contribute to memory by stabilizing perineuronal nets in the dorsohippocampal CA1 subfield, as revealed by targeted disruptions of the primary cilium or perineuronal nets. The findings show that nonsynaptic, primary cilium-mediated mechanisms are required for the persistence of context memory.
AB - It is well established that the formation of episodic memories requires multiple hippocampal mechanisms operating on different time scales. Early mechanisms of memory formation (synaptic consolidation) have been extensively characterized. However, delayed mechanisms, which maintain hippocampal activity as memories stabilize in cortical circuits, are not well understood. Here we demonstrate that contrary to the transient expression of early- and delayed-response genes, the expression of cytoskeleton- and extracellular matrix-associated genes remains dynamic even at remote time points. The most profound expression changes clustered around primary cilium-associated and collagen genes. These genes most likely contribute to memory by stabilizing perineuronal nets in the dorsohippocampal CA1 subfield, as revealed by targeted disruptions of the primary cilium or perineuronal nets. The findings show that nonsynaptic, primary cilium-mediated mechanisms are required for the persistence of context memory.
KW - Cellular neuroscience
KW - Cognitive neuroscience
KW - Neuroscience
UR - http://www.scopus.com/inward/record.url?scp=85109041006&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85109041006&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2021.102617
DO - 10.1016/j.isci.2021.102617
M3 - Article
AN - SCOPUS:85109041006
SN - 2589-0042
VL - 24
JO - iScience
JF - iScience
IS - 6
M1 - 102617
ER -