Unmasking Proteolytic Activity for Adult Visual Cortex Plasticity by the Removal of Lynx1.

dc.contributor.author

Bukhari, Noreen

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Burman, Poromendro N

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Hussein, Ayan

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Demars, Michael P

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Sadahiro, Masato

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Brady, Daniel M

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Tsirka, Stella E

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Russo, Scott J

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Morishita, Hirofumi

dc.date.accessioned

2021-04-01T19:02:15Z

dc.date.available

2021-04-01T19:02:15Z

dc.date.issued

2015-09

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2021-04-01T19:02:15Z

dc.description.abstract

Unlabelled

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.

Significance statement

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.
dc.identifier

35/37/12693

dc.identifier.issn

0270-6474

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1529-2401

dc.identifier.uri

https://hdl.handle.net/10161/22507

dc.language

eng

dc.publisher

Society for Neuroscience

dc.relation.ispartof

The Journal of neuroscience : the official journal of the Society for Neuroscience

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10.1523/jneurosci.4315-14.2015

dc.subject

Visual Cortex

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Dendritic Spines

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Animals

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Mice, Inbred C57BL

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Mice, Knockout

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Mice

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Blindness

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Tissue Plasminogen Activator

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Neuropeptides

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Membrane Glycoproteins

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Nerve Tissue Proteins

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Sensory Deprivation

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Environment

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Housing, Animal

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Action Potentials

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Aging

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Neuronal Plasticity

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Dominance, Ocular

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Genes, Reporter

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Female

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Male

dc.title

Unmasking Proteolytic Activity for Adult Visual Cortex Plasticity by the Removal of Lynx1.

dc.type

Journal article

pubs.begin-page

12693

pubs.end-page

12702

pubs.issue

37

pubs.organisational-group

School of Medicine

pubs.organisational-group

Duke Institute for Brain Sciences

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Neurology, Movement Disorders

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Duke

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University Institutes and Centers

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Institutes and Provost's Academic Units

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Neurology

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Clinical Science Departments

pubs.publication-status

Published

pubs.volume

35

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