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Roles of heat shock factor 1 in neuronal response to fetal environmental risks and its relevance to brain disorders.


ABSTRACT: Prenatal exposure of the developing brain to various environmental challenges increases susceptibility to late onset of neuropsychiatric dysfunction; still, the underlying mechanisms remain obscure. Here we show that exposure of embryos to a variety of environmental factors such as alcohol, methylmercury, and maternal seizure activates HSF1 in cerebral cortical cells. Furthermore, Hsf1 deficiency in the mouse cortex exposed in utero to subthreshold levels of these challenges causes structural abnormalities and increases seizure susceptibility after birth. In addition, we found that human neural progenitor cells differentiated from induced pluripotent stem cells derived from schizophrenia patients show higher variability in the levels of HSF1 activation induced by environmental challenges compared to controls. We propose that HSF1 plays a crucial role in the response of brain cells to prenatal environmental insults and may be a key component in the pathogenesis of late-onset neuropsychiatric disorders.

SUBMITTER: Hashimoto-Torii K 

PROVIDER: S-EPMC4051437 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

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Roles of heat shock factor 1 in neuronal response to fetal environmental risks and its relevance to brain disorders.

Hashimoto-Torii Kazue K   Torii Masaaki M   Fujimoto Mitsuaki M   Nakai Akira A   El Fatimy Rachid R   Mezger Valerie V   Ju Min J MJ   Ishii Seiji S   Chao Shih-Hui SH   Brennand Kristen J KJ   Gage Fred H FH   Rakic Pasko P  

Neuron 20140410 3


Prenatal exposure of the developing brain to various environmental challenges increases susceptibility to late onset of neuropsychiatric dysfunction; still, the underlying mechanisms remain obscure. Here we show that exposure of embryos to a variety of environmental factors such as alcohol, methylmercury, and maternal seizure activates HSF1 in cerebral cortical cells. Furthermore, Hsf1 deficiency in the mouse cortex exposed in utero to subthreshold levels of these challenges causes structural ab  ...[more]

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