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Mouse brain transcriptome responses to inhaled nanoparticulate matter differed by sex and APOE in Nrf2-Nfkb interactions.


ABSTRACT: The neurotoxicity of air pollution is undefined for sex and APOE alleles. These major risk factors of Alzheimer's disease (AD) were examined in mice given chronic exposure to nPM, a nano-sized subfraction of urban air pollution. In the cerebral cortex, female mice had two-fold more genes responding to nPM than males. Transcriptomic responses to nPM had sex-APOE interactions in AD-relevant pathways. Only APOE3 mice responded to nPM in genes related to Abeta deposition and clearance (Vav2, Vav3, S1009a). Other responding genes included axonal guidance, inflammation (AMPK, NFKB, APK/JNK signaling), and antioxidant signaling (NRF2, HIF1A). Genes downstream of NFKB and NRF2 responded in opposite directions to nPM. Nrf2 knockdown in microglia augmented NFKB responses to nPM, suggesting a critical role of NRF2 in air pollution neurotoxicity. These findings give a rationale for epidemiologic studies of air pollution to consider sex interactions with APOE alleles and other AD-risk genes.

SUBMITTER: Haghani A 

PROVIDER: S-EPMC7314548 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Mouse brain transcriptome responses to inhaled nanoparticulate matter differed by sex and <i>APOE</i> in <i>Nrf2-Nfkb</i> interactions.

Haghani Amin A   Cacciottolo Mafalda M   Doty Kevin R KR   D'Agostino Carla C   Thorwald Max M   Safi Nikoo N   Levine Morgan E ME   Sioutas Constantinos C   Town Terrence C TC   Forman Henry Jay HJ   Zhang Hongqiao H   Morgan Todd E TE   Finch Caleb E CE  

eLife 20200624


The neurotoxicity of air pollution is undefined for sex and <i>APOE</i> alleles. These major risk factors of Alzheimer's disease (AD) were examined in mice given chronic exposure to nPM, a nano-sized subfraction of urban air pollution. In the cerebral cortex, female mice had two-fold more genes responding to nPM than males. Transcriptomic responses to nPM had sex-<i>APOE</i> interactions in AD-relevant pathways. Only <i>APOE</i>3 mice responded to nPM in genes related to Abeta deposition and cle  ...[more]

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