Neuronal theories of neurodevelopmental disorders (NDDs) of autism and mental retardation propose that abnormal connectivity underlies deficits in attentional processing. We tested this theory by studying unitary synaptic connections between layer 5 pyramidal neurons within medial prefrontal cortex (mPFC) networks in the Fmr1-KO mouse model for mental retardation and autism. In line with predictions from neurocognitive theory, we found that neighboring pyramidal neurons were hyperconnected during a critical period in early mPFC development. Surprisingly, excitatory synaptic connections between Fmr1-KO pyramidal neurons were significantly slower and failed to recover from short-term depression as quickly as wild type (WT) synapses. By 4-5 weeks of mPFC development, connectivity rates were identical for both KO and WT pyramidal neurons and synapse dynamics changed from depressing to facilitating responses with similar properties in both groups. We propose that the early alteration in connectivity and synaptic recovery are tightly linked: using a network model, we show that slower synapses are essential to counterbalance hyperconnectivity in order to maintain a dynamic range of excitatory activity. However, the slow synaptic time constants induce decreased responsiveness to low-frequency stimulation, which may explain deficits in integration and early information processing in attentional neuronal networks in NDDs. © 2011 The Author.

Hyperconnectivity and slow synapses during early development of medial prefrontal cortex in a mouse model for mental retardation and Autism / Testa-Silva, G.; Loebel, A.; Giugliano, M.; De Kock, C. P. J.; Mansvelder, H. D.; Meredith, R. M.. - In: CEREBRAL CORTEX. - ISSN 1047-3211. - 22:6(2012), pp. 1333-1342. [10.1093/cercor/bhr224]

Hyperconnectivity and slow synapses during early development of medial prefrontal cortex in a mouse model for mental retardation and Autism

Giugliano, M.;
2012-01-01

Abstract

Neuronal theories of neurodevelopmental disorders (NDDs) of autism and mental retardation propose that abnormal connectivity underlies deficits in attentional processing. We tested this theory by studying unitary synaptic connections between layer 5 pyramidal neurons within medial prefrontal cortex (mPFC) networks in the Fmr1-KO mouse model for mental retardation and autism. In line with predictions from neurocognitive theory, we found that neighboring pyramidal neurons were hyperconnected during a critical period in early mPFC development. Surprisingly, excitatory synaptic connections between Fmr1-KO pyramidal neurons were significantly slower and failed to recover from short-term depression as quickly as wild type (WT) synapses. By 4-5 weeks of mPFC development, connectivity rates were identical for both KO and WT pyramidal neurons and synapse dynamics changed from depressing to facilitating responses with similar properties in both groups. We propose that the early alteration in connectivity and synaptic recovery are tightly linked: using a network model, we show that slower synapses are essential to counterbalance hyperconnectivity in order to maintain a dynamic range of excitatory activity. However, the slow synaptic time constants induce decreased responsiveness to low-frequency stimulation, which may explain deficits in integration and early information processing in attentional neuronal networks in NDDs. © 2011 The Author.
2012
22
6
1333
1342
https://doi.org/10.1093/CERCOR/BHR224
Testa-Silva, G.; Loebel, A.; Giugliano, M.; De Kock, C. P. J.; Mansvelder, H. D.; Meredith, R. M.
File in questo prodotto:
File Dimensione Formato  
testa-silva2011.pdf

non disponibili

Descrizione: Articolo principale
Tipologia: Versione Editoriale (PDF)
Licenza: Non specificato
Dimensione 825.96 kB
Formato Adobe PDF
825.96 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11767/99660
Citazioni
  • ???jsp.display-item.citation.pmc??? 70
  • Scopus 90
  • ???jsp.display-item.citation.isi??? 89
social impact