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Estradiol reverses excitatory synapse loss in a cellular model of neuropsychiatric disorders.


ABSTRACT: Loss of glutamatergic synapses is thought to be a key cellular pathology associated with neuropsychiatric disorders including schizophrenia (SCZ) and major depressive disorder (MDD). Genetic and cellular studies of SCZ and MDD using in vivo and in vitro systems have supported a key role for dysfunction of excitatory synapses in the pathophysiology of these disorders. Recent clinical studies have demonstrated that the estrogen, 17?-estradiol can ameliorate many of the symptoms experienced by patients. Yet, to date, our understanding of how 17?-estradiol exerted these beneficial effects is limited. In this study, we have tested the hypothesis that 17?-estradiol can restore dendritic spine number in a cellular model that recapitulates the loss of synapses associated with SCZ and MDD. Ectopic expression of wildtype, mutant or shRNA-mediated knockdown of Disrupted in Schizophrenia 1 (DISC1) reduced dendritic spine density in primary cortical neurons. Acute or chronic treatment with 17?-estradiol increased spine density to control levels in neurons with altered DISC1 levels. In addition, 17?-estradiol reduced the extent to which ectopic wildtype and mutant DISC1 aggregated. Furthermore, 17?-estradiol also caused the enrichment of synaptic proteins at synapses and increased the number of dendritic spines containing PSD-95 or that overlapped with the pre-synaptic marker bassoon. Taken together, our data indicates that estrogens can restore lost excitatory synapses caused by altered DISC1 expression, potentially through the trafficking of DISC1 and its interacting partners. These data highlight the possibility that estrogens exert their beneficial effects in SCZ and MDD in part by modulating dendritic spine number.

SUBMITTER: Erli F 

PROVIDER: S-EPMC7026123 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Estradiol reverses excitatory synapse loss in a cellular model of neuropsychiatric disorders.

Erli Filippo F   Palmos Alish B AB   Raval Pooja P   Mukherjee Jayanta J   Sellers Katherine J KJ   Gatford Nicholas J F NJF   Moss Stephen J SJ   Brandon Nicholas J NJ   Penzes Peter P   Srivastava Deepak P DP  

Translational psychiatry 20200121 1


Loss of glutamatergic synapses is thought to be a key cellular pathology associated with neuropsychiatric disorders including schizophrenia (SCZ) and major depressive disorder (MDD). Genetic and cellular studies of SCZ and MDD using in vivo and in vitro systems have supported a key role for dysfunction of excitatory synapses in the pathophysiology of these disorders. Recent clinical studies have demonstrated that the estrogen, 17β-estradiol can ameliorate many of the symptoms experienced by pati  ...[more]

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