Unmasking Proteolytic Activity for Adult Visual Cortex Plasticity by the Removal of Lynx1.
Abstract
<h4>Unlabelled</h4>Experience-dependent cortical plasticity declines with age. At
the molecular level, experience-dependent proteolytic activity of tissue plasminogen
activator (tPA) becomes restricted in the adult brain if mice are raised in standard
cages. Understanding the mechanism for the loss of permissive proteolytic activity
is therefore a key link for improving function in adult brains. Using the mouse primary
visual cortex (V1) as a model, we demonstrate that tPA activity in V1 can be unmasked
following 4 d of monocular deprivation when the mice older than 2 months are raised
in standard cages by the genetic removal of Lynx1, a negative regulator of adult plasticity.
This was also associated with the reduction of stubby and thin spine density and enhancement
of ocular dominance shift in adult V1 of Lynx1 knock-out (KO) mice. These structural
and functional changes were tPA-dependent because genetic removal of tPA in Lynx1
KO mice can block the monocular deprivation-dependent reduction of dendritic spine
density, whereas both genetic and adult specific inhibition of tPA activity can ablate
the ocular dominance shift in Lynx1 KO mice. Our work demonstrates that the adult
brain has an intrinsic potential for experience-dependent elevation of proteolytic
activity to express juvenile-like structural and functional changes but is effectively
limited by Lynx1 if mice are raised in standard cages. Insights into the Lynx1-tPA
plasticity mechanism may provide novel therapeutic targets for adult brain disorders.<h4>Significance
statement</h4>Experience-dependent proteolytic activity of tissue plasminogen activator
(tPA) becomes restricted in the adult brain in correlation with the decline in cortical
plasticity when mice are raised in standard cages. We demonstrated that removal of
Lynx1, one of negative regulators of plasticity, unmasks experience-dependent tPA
elevation in visual cortex of adult mice reared in standard cages. This proteolytic
elevation facilitated dendritic spine reduction and ocular dominance plasticity in
adult visual cortex. This is the first demonstration of adult brain to retain the
intrinsic capacity to elevate tPA in an experience-dependent manner but is effectively
limited by Lynx1. tPA-Lynx1 may potentially be a new candidate mechanism for interventions
that were shown to activate plasticity in adult brain.
Type
Journal articleSubject
Visual CortexDendritic Spines
Animals
Mice, Inbred C57BL
Mice, Knockout
Mice
Blindness
Tissue Plasminogen Activator
Neuropeptides
Membrane Glycoproteins
Nerve Tissue Proteins
Sensory Deprivation
Environment
Housing, Animal
Action Potentials
Aging
Neuronal Plasticity
Dominance, Ocular
Genes, Reporter
Female
Male
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https://hdl.handle.net/10161/22507Published Version (Please cite this version)
10.1523/jneurosci.4315-14.2015Publication Info
Bukhari, Noreen; Burman, Poromendro N; Hussein, Ayan; Demars, Michael P; Sadahiro,
Masato; Brady, Daniel M; ... Morishita, Hirofumi (2015). Unmasking Proteolytic Activity for Adult Visual Cortex Plasticity by the Removal of
Lynx1. The Journal of neuroscience : the official journal of the Society for Neuroscience, 35(37). pp. 12693-12702. 10.1523/jneurosci.4315-14.2015. Retrieved from https://hdl.handle.net/10161/22507.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Noreen Bukhari-Parlakturk
Assistant Professor of Neurology
I have a long standing interest in developing disease-modifying therapies for movement
disorders, a major unmet clinical need. I work at the interface of neuroscience and
neurology to apply mechanistic understanding of neurological disease to develop targeted
neuromodulatory therapies and in the process further disease mechanisms and medical
therapy.

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