» Articles » PMID: 26594141

Autism Spectrum Disorders and Neuropathology of the Cerebellum

Overview
Journal Front Neurosci
Date 2015 Nov 24
PMID 26594141
Citations 106
Authors
Affiliations
Soon will be listed here.
Abstract

The cerebellum contains the largest number of neurons and synapses of any structure in the central nervous system. The concept that the cerebellum is solely involved in fine motor function has become outdated; substantial evidence has accumulated linking the cerebellum with higher cognitive functions including language. Cerebellar deficits have been implicated in autism for more than two decades. The computational power of the cerebellum is essential for many, if not most of the processes that are perturbed in autism including language and communication, social interactions, stereotyped behavior, motor activity and motor coordination, and higher cognitive functions. The link between autism and cerebellar dysfunction should not be surprising to those who study its cellular, physiological, and functional properties. Postmortem studies have revealed neuropathological abnormalities in cerebellar cellular architecture while studies on mouse lines with cell loss or mutations in single genes restricted to cerebellar Purkinje cells have also strongly implicated this brain structure in contributing to the autistic phenotype. This connection has been further substantiated by studies investigating brain damage in humans restricted to the cerebellum. In this review, we summarize advances in research on idiopathic autism and three genetic forms of autism that highlight the key roles that the cerebellum plays in this spectrum of neurodevelopmental disorders.

Citing Articles

Cerebellar Alterations in Autism Spectrum Disorder: A Mini-Review.

Rodrigues B, Silva J, Kawamoto E Cerebellum. 2025; 24(2):52.

PMID: 39985593 DOI: 10.1007/s12311-025-01806-1.


Behavioral decline in Shank3 mice during early adulthood parallels cerebellar granule cell glutamatergic synaptic changes.

Kshetri R, Beavers J, Hyde R, Ewa R, Schwertman A, Porcayo S Mol Autism. 2024; 15(1):52.

PMID: 39633421 PMC: 11616285. DOI: 10.1186/s13229-024-00628-y.


Engrailed-2 and inflammation convergently and independently impinge on cerebellar Purkinje cell differentiation.

Bahaaeldin M, Bulte C, Luelsberg F, Kumar S, Kappler J, Volker C J Neuroinflammation. 2024; 21(1):306.

PMID: 39609827 PMC: 11603920. DOI: 10.1186/s12974-024-03301-6.


The Cerebellum-Ventral Tegmental Area Microcircuit and Its Implications for Autism Spectrum Disorder: A Narrative Review.

Zhou P, Peng S, Wen S, Lan Q, Zhuang Y, Li X Neuropsychiatr Dis Treat. 2024; 20:2039-2048.

PMID: 39494383 PMC: 11531233. DOI: 10.2147/NDT.S485487.


Multiunit Recording of Cerebellar Cortex in Autistic Male Rats during Social Interaction in Enriched Environments.

Cruz-Magos O, Herrera-Meza G, Garcia L, Coria-Avila G, Herrera-Covarrubias D, Toledo-Cardenas M NeuroSci. 2024; 4(3):178-185.

PMID: 39483200 PMC: 11523729. DOI: 10.3390/neurosci4030016.


References
1.
Ellegood J, Pacey L, Hampson D, Lerch J, Henkelman R . Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging. Neuroimage. 2010; 53(3):1023-9. DOI: 10.1016/j.neuroimage.2010.03.038. View

2.
Casanova M, Buxhoeveden D, Switala A, Roy E . Rett syndrome as a minicolumnopathy. Clin Neuropathol. 2003; 22(4):163-8. View

3.
Betancur C . Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res. 2010; 1380:42-77. DOI: 10.1016/j.brainres.2010.11.078. View

4.
Steadman P, Ellegood J, Szulc K, Turnbull D, Joyner A, Henkelman R . Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas. Autism Res. 2013; 7(1):124-37. PMC: 4418792. DOI: 10.1002/aur.1344. View

5.
Ertan G, Arulrajah S, Tekes A, Jordan L, Huisman T . Cerebellar abnormality in children and young adults with tuberous sclerosis complex: MR and diffusion weighted imaging findings. J Neuroradiol. 2010; 37(4):231-8. DOI: 10.1016/j.neurad.2009.12.006. View