Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism

Thomas C. Jaramillo, Haley E. Speed, Zhong Xuan, Jeremy M. Reimers, Shunan Liu, Craig M. Powell

Research output: Contribution to journalArticle

54 Citations (Scopus)

Abstract

Shank3 is a multi-domain, synaptic scaffolding protein that organizes proteins in the postsynaptic density of excitatory synapses. Clinical studies suggest that ∼0.5% of autism spectrum disorder (ASD) cases may involve SHANK3 mutation/deletion. Patients with SHANK3 mutations exhibit deficits in cognition along with delayed/impaired speech/language and repetitive and obsessive/compulsive-like (OCD-like) behaviors. To examine how mutation/deletion of SHANK3 might alter brain function leading to ASD, we have independently created mice with deletion of Shank3 exons 4-9, a region implicated in ASD patients. We find that homozygous deletion of exons 4-9 (Shank3e4-9 KO) results in loss of the two highest molecular weight isoforms of Shank3 and a significant reduction in other isoforms. Behaviorally, both Shank3e4-9 heterozygous (HET) and Shank3e4-9 KO mice display increased repetitive grooming, deficits in novel and spatial object recognition learning and memory, and abnormal ultrasonic vocalizations. Shank3e4-9 KO mice also display abnormal social interaction when paired with one another. Analysis of synaptosome fractions from striata of Shank3e4-9 KO mice reveals decreased Homer1b/c, GluA2, and GluA3 expression. Both Shank3e4-9 HET and KO demonstrated a significant reduction in NMDA/AMPA ratio at excitatory synapses onto striatal medium spiny neurons. Furthermore, Shank3e4-9 KO mice displayed reduced hippocampal LTP despite normal baseline synaptic transmission. Collectively these behavioral, biochemical and physiological changes suggest Shank3 isoforms have region-specific roles in regulation of AMPAR subunit localization and NMDAR function in the Shank3e4-9 mutant mouse model of autism.

Original languageEnglish (US)
Pages (from-to)350-375
Number of pages26
JournalAutism Research
Volume9
Issue number3
DOIs
StatePublished - Mar 1 2016

Fingerprint

Corpus Striatum
Autistic Disorder
Protein Isoforms
Sequence Deletion
Synapses
Exons
Grooming
alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
Synaptosomes
N-Methylaspartate
Interpersonal Relations
Ultrasonics
Synaptic Transmission
Cognition
Language
Molecular Weight
Learning
Neurons
Mutation
Brain

Keywords

  • Autism spectrum disorder
  • Grooming
  • Mouse model
  • Phelan-McDermid syndrome
  • Shank3

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology
  • Genetics(clinical)

Cite this

Jaramillo, T. C., Speed, H. E., Xuan, Z., Reimers, J. M., Liu, S., & Powell, C. M. (2016). Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism. Autism Research, 9(3), 350-375. https://doi.org/10.1002/aur.1529

Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism. / Jaramillo, Thomas C.; Speed, Haley E.; Xuan, Zhong; Reimers, Jeremy M.; Liu, Shunan; Powell, Craig M.

In: Autism Research, Vol. 9, No. 3, 01.03.2016, p. 350-375.

Research output: Contribution to journalArticle

Jaramillo, TC, Speed, HE, Xuan, Z, Reimers, JM, Liu, S & Powell, CM 2016, 'Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism', Autism Research, vol. 9, no. 3, pp. 350-375. https://doi.org/10.1002/aur.1529
Jaramillo, Thomas C. ; Speed, Haley E. ; Xuan, Zhong ; Reimers, Jeremy M. ; Liu, Shunan ; Powell, Craig M. / Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism. In: Autism Research. 2016 ; Vol. 9, No. 3. pp. 350-375.
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