» Articles » PMID: 22238087

Alteration of Synaptic Network Dynamics by the Intellectual Disability Protein PAK3

Overview
Journal J Neurosci
Specialty Neurology
Date 2012 Jan 13
PMID 22238087
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Several gene mutations linked to intellectual disability in humans code for synaptic molecules implicated in small GTPase signaling. This is the case of the Rac/Cdc42 effector p21-activated kinase 3 (PAK3). The mechanisms responsible for the intellectual defects and the consequences of the mutation on the development and wiring of brain networks remain unknown. Here we show that expression of PAK3 mutants, suppression of PAK3, or inhibition of PAK3 function in rat hippocampal slice cultures interfere with activity-mediated spine dynamics. Inhibition of PAK3 resulted in two main alterations: (1) an increased growth of new, unstable spines, occurring in clusters, and mediated by activity; and (2) an impairment of plasticity-mediated spine stabilization interfering with the formation of persistent spines. Additionally, we find that PAK3 is specifically recruited by activity from dendrites into spines, providing a new mechanism through which PAK3 could participate in the control of both spine stabilization and local spine growth. Together, these data identify a novel function of PAK3 in regulating activity-mediated rearrangement of synaptic connectivity associated with learning and suggest that defects in spine formation and refinement during development could account for intellectual disability.

Citing Articles

Aging activates escape of the silent X chromosome in the female mouse hippocampus.

Gadek M, Shaw C, Abdulai-Saiku S, Saloner R, Marino F, Wang D Sci Adv. 2025; 11(10):eads8169.

PMID: 40043106 PMC: 11881916. DOI: 10.1126/sciadv.ads8169.


Intracellular spatial transcriptomic analysis toolkit (InSTAnT).

Kumar A, Schrader A, Aggarwal B, Boroojeny A, Asadian M, Lee J Nat Commun. 2024; 15(1):7794.

PMID: 39242579 PMC: 11379969. DOI: 10.1038/s41467-024-49457-w.


The molecular basis of p21-activated kinase-associated neurodevelopmental disorders: From genotype to phenotype.

Dobrigna M, Poea-Guyon S, Rousseau V, Vincent A, Toutain A, Barnier J Front Neurosci. 2023; 17:1123784.

PMID: 36937657 PMC: 10017488. DOI: 10.3389/fnins.2023.1123784.


Pharmacological Inhibition of p-21 Activated Kinase (PAK) Restores Impaired Neurite Outgrowth and Remodeling in a Cellular Model of Down Syndrome.

Barraza-Nunez N, Perez-Nunez R, Gaete-Ramirez B, Barrios-Garrido A, Arriagada C, Poksay K Neurotox Res. 2023; 41(3):256-269.

PMID: 36867391 DOI: 10.1007/s12640-023-00638-3.


Genomic legacy of migration in endangered caribou.

Cavedon M, vonHoldt B, Hebblewhite M, Hegel T, Heppenheimer E, Hervieux D PLoS Genet. 2022; 18(2):e1009974.

PMID: 35143486 PMC: 8830729. DOI: 10.1371/journal.pgen.1009974.


References
1.
Xie Z, Srivastava D, Photowala H, Kai L, Cahill M, Woolfrey K . Kalirin-7 controls activity-dependent structural and functional plasticity of dendritic spines. Neuron. 2007; 56(4):640-56. PMC: 2118058. DOI: 10.1016/j.neuron.2007.10.005. View

2.
Zhang H, Webb D, Asmussen H, Niu S, Horwitz A . A GIT1/PIX/Rac/PAK signaling module regulates spine morphogenesis and synapse formation through MLC. J Neurosci. 2005; 25(13):3379-88. PMC: 6724907. DOI: 10.1523/JNEUROSCI.3553-04.2005. View

3.
Hashimoto S, Tsubouchi A, Mazaki Y, Sabe H . Interaction of paxillin with p21-activated Kinase (PAK). Association of paxillin alpha with the kinase-inactive and the Cdc42-activated forms of PAK3. J Biol Chem. 2000; 276(8):6037-45. DOI: 10.1074/jbc.M005854200. View

4.
Holtmaat A, Svoboda K . Experience-dependent structural synaptic plasticity in the mammalian brain. Nat Rev Neurosci. 2009; 10(9):647-58. DOI: 10.1038/nrn2699. View

5.
Mateos J, Luthi A, Savic N, Stierli B, Streit P, Gahwiler B . Synaptic modifications at the CA3-CA1 synapse after chronic AMPA receptor blockade in rat hippocampal slices. J Physiol. 2007; 581(Pt 1):129-38. PMC: 2075211. DOI: 10.1113/jphysiol.2006.120550. View