» Articles » PMID: 25578949

Dendritic Spine Dysgenesis in Autism Related Disorders

Overview
Journal Neurosci Lett
Specialty Neurology
Date 2015 Jan 13
PMID 25578949
Citations 93
Authors
Affiliations
Soon will be listed here.
Abstract

The activity-dependent structural and functional plasticity of dendritic spines has led to the long-standing belief that these neuronal compartments are the subcellular sites of learning and memory. Of relevance to human health, central neurons in several neuropsychiatric illnesses, including autism related disorders, have atypical numbers and morphologies of dendritic spines. These so-called dendritic spine dysgeneses found in individuals with autism related disorders are consistently replicated in experimental mouse models. Dendritic spine dysgenesis reflects the underlying synaptopathology that drives clinically relevant behavioral deficits in experimental mouse models, providing a platform for testing new therapeutic approaches. By examining molecular signaling pathways, synaptic deficits, and spine dysgenesis in experimental mouse models of autism related disorders we find strong evidence for mTOR to be a critical point of convergence and promising therapeutic target.

Citing Articles

Developmental deficits, synapse and dendritic abnormalities in a Clcn4 KO autism mice model: endophenotypic target for ASD.

Lee S, Choi Y, Kim D, Jeong H, Do Y, Jung S Transl Psychiatry. 2025; 15(1):28.

PMID: 39863599 PMC: 11762770. DOI: 10.1038/s41398-024-03201-6.


The potential ameliorative effect of mesenchymal stem cells-derived exosomes on cerebellar histopathology and their modifying role on PI3k-mTOR signaling in rat model of autism spectrum disorder.

Elsherif R, Mm Abdel-Hafez A, Hussein O, Sabry D, Abdelzaher L, Bayoumy A J Mol Histol. 2025; 56(1):65.

PMID: 39760823 DOI: 10.1007/s10735-024-10335-w.


Deciphering the Role of Shank3 in Dendritic Morphology and Synaptic Function Across Postnatal Developmental Stages in the Shank3B KO Mouse.

Yang J, Ma G, Du X, Xie J, Wang M, Wang W Neurosci Bull. 2024; .

PMID: 39693031 DOI: 10.1007/s12264-024-01330-y.


Mutation in the mitochondrial chaperone TRAP1 leads to autism with more severe symptoms in males.

Rydzanicz M, Kuzniewska B, Magnowska M, Wojtowicz T, Stawikowska A, Hojka A EMBO Mol Med. 2024; 16(11):2976-3004.

PMID: 39333440 PMC: 11554806. DOI: 10.1038/s44321-024-00147-6.


Clinical-grade intranasal NGF fuels neurological and metabolic functions of Mecp2-deficient mice.

Pozzer D, Indrigo M, Breccia M, Florio E, Franchino C, De Rocco G Brain. 2024; 148(3):845-860.

PMID: 39300821 PMC: 11884770. DOI: 10.1093/brain/awae291.


References
1.
Tang G, Gudsnuk K, Kuo S, Cotrina M, Rosoklija G, Sosunov A . Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits. Neuron. 2014; 83(5):1131-43. PMC: 4159743. DOI: 10.1016/j.neuron.2014.07.040. View

2.
Chevere-Torres I, Kaphzan H, Bhattacharya A, Kang A, Maki J, Gambello M . Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex. Neurobiol Dis. 2011; 45(3):1101-10. PMC: 3276695. DOI: 10.1016/j.nbd.2011.12.028. View

3.
Chapleau C, Calfa G, Lane M, Albertson A, Larimore J, Kudo S . Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations. Neurobiol Dis. 2009; 35(2):219-33. PMC: 2722110. DOI: 10.1016/j.nbd.2009.05.001. View

4.
Jay V, Becker L, Chan F, Perry Sr T . Puppet-like syndrome of Angelman: a pathologic and neurochemical study. Neurology. 1991; 41(3):416-22. DOI: 10.1212/wnl.41.3.416. View

5.
Kandt R, Haines J, Smith M, Northrup H, Gardner R, Short M . Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nat Genet. 1992; 2(1):37-41. DOI: 10.1038/ng0992-37. View