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Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition

Negative allosteric modulators, such as lynx1 and lynx2, directly interact with nicotinic acetylcholine receptors (nAChRs). The nAChRs are integral to cholinergic signaling in the brain and have been shown to mediate different aspects of cognitive function. Given the interaction between lynx protein...

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Autores principales: Sherafat, Yasmine, Chen, Edison, Lallai, Valeria, Bautista, Malia, Fowler, James P., Chen, Yen-Chu, Miwa, Julie, Fowler, Christie D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595198/
https://www.ncbi.nlm.nih.gov/pubmed/34803621
http://dx.doi.org/10.3389/fnbeh.2021.703748
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author Sherafat, Yasmine
Chen, Edison
Lallai, Valeria
Bautista, Malia
Fowler, James P.
Chen, Yen-Chu
Miwa, Julie
Fowler, Christie D.
author_facet Sherafat, Yasmine
Chen, Edison
Lallai, Valeria
Bautista, Malia
Fowler, James P.
Chen, Yen-Chu
Miwa, Julie
Fowler, Christie D.
author_sort Sherafat, Yasmine
collection PubMed
description Negative allosteric modulators, such as lynx1 and lynx2, directly interact with nicotinic acetylcholine receptors (nAChRs). The nAChRs are integral to cholinergic signaling in the brain and have been shown to mediate different aspects of cognitive function. Given the interaction between lynx proteins and these receptors, we examined whether these endogenous negative allosteric modulators are involved in cognitive behaviors associated with cholinergic function. We found both cell-specific and overlapping expression patterns of lynx1 and lynx2 mRNA in brain regions associated with cognition, learning, memory, and sensorimotor processing, including the prefrontal cortex (PFC), cingulate cortex, septum, hippocampus, amygdala, striatum, and pontine nuclei. Since lynx proteins are thought to play a role in conditioned associations and given the expression patterns across brain regions, we first assessed whether lynx knockout mice would differ in a cognitive flexibility task. We found no deficits in reversal learning in either the lynx1(–/–) or lynx2(–/–) knockout mice. Thereafter, sensorimotor gating was examined with the prepulse inhibition (PPI) assessment. Interestingly, we found that both male and female lynx1(–/–) mice exhibited a deficit in the PPI behavioral response. Given the comparable expression of lynx2 in regions involved in sensorimotor gating, we then examined whether removal of the lynx2 protein would lead to similar behavioral effects. Unexpectedly, we found that while male lynx2(–/–) mice exhibited a decrease in the baseline startle response, no differences were found in sensorimotor gating for either male or female lynx2(–/–) mice. Taken together, these studies provide insight into the expression patterns of lynx1 and lynx2 across multiple brain regions and illustrate the modulatory effects of the lynx1 protein in sensorimotor gating.
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spelling pubmed-85951982021-11-18 Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition Sherafat, Yasmine Chen, Edison Lallai, Valeria Bautista, Malia Fowler, James P. Chen, Yen-Chu Miwa, Julie Fowler, Christie D. Front Behav Neurosci Neuroscience Negative allosteric modulators, such as lynx1 and lynx2, directly interact with nicotinic acetylcholine receptors (nAChRs). The nAChRs are integral to cholinergic signaling in the brain and have been shown to mediate different aspects of cognitive function. Given the interaction between lynx proteins and these receptors, we examined whether these endogenous negative allosteric modulators are involved in cognitive behaviors associated with cholinergic function. We found both cell-specific and overlapping expression patterns of lynx1 and lynx2 mRNA in brain regions associated with cognition, learning, memory, and sensorimotor processing, including the prefrontal cortex (PFC), cingulate cortex, septum, hippocampus, amygdala, striatum, and pontine nuclei. Since lynx proteins are thought to play a role in conditioned associations and given the expression patterns across brain regions, we first assessed whether lynx knockout mice would differ in a cognitive flexibility task. We found no deficits in reversal learning in either the lynx1(–/–) or lynx2(–/–) knockout mice. Thereafter, sensorimotor gating was examined with the prepulse inhibition (PPI) assessment. Interestingly, we found that both male and female lynx1(–/–) mice exhibited a deficit in the PPI behavioral response. Given the comparable expression of lynx2 in regions involved in sensorimotor gating, we then examined whether removal of the lynx2 protein would lead to similar behavioral effects. Unexpectedly, we found that while male lynx2(–/–) mice exhibited a decrease in the baseline startle response, no differences were found in sensorimotor gating for either male or female lynx2(–/–) mice. Taken together, these studies provide insight into the expression patterns of lynx1 and lynx2 across multiple brain regions and illustrate the modulatory effects of the lynx1 protein in sensorimotor gating. Frontiers Media S.A. 2021-11-03 /pmc/articles/PMC8595198/ /pubmed/34803621 http://dx.doi.org/10.3389/fnbeh.2021.703748 Text en Copyright © 2021 Sherafat, Chen, Lallai, Bautista, Fowler, Chen, Miwa and Fowler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Sherafat, Yasmine
Chen, Edison
Lallai, Valeria
Bautista, Malia
Fowler, James P.
Chen, Yen-Chu
Miwa, Julie
Fowler, Christie D.
Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title_full Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title_fullStr Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title_full_unstemmed Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title_short Differential Expression Patterns of Lynx Proteins and Involvement of Lynx1 in Prepulse Inhibition
title_sort differential expression patterns of lynx proteins and involvement of lynx1 in prepulse inhibition
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595198/
https://www.ncbi.nlm.nih.gov/pubmed/34803621
http://dx.doi.org/10.3389/fnbeh.2021.703748
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