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Series GSE75208 Query DataSets for GSE75208
Status Public on Dec 31, 2015
Title Estrogenic compounds reduce influenza A virus replication in primary human nasal epithelial cells derived from female, but not male, donors
Organism Homo sapiens
Experiment type Expression profiling by array
Summary E2 exposure significantly decreased peak viral titer in hNECs from female donors. We used microarray analyses to identify global gene expression patterns between E2 and vehicle exposed hNECs from female donors
Influenza causes an acute infection characterized by virus replication in respiratory epithelial cells. The severity of influenza and other respiratory diseases changes over the life course and during pregnancy in women, suggesting that sex steroid hormones, such as estrogens, may be involved. Using primary, differentiated human nasal epithelial cell (hNEC) cultures from adult male and female donors, we exposed cultures to the endogenous 17β-estradiol (E2) or select estrogen receptor modulators (SERMs), then infected cultures with a seasonal influenza A virus (IAV) to determine whether estrogenic signaling could affect the outcome of IAV infection and whether these effects where sex-dependent. Estradiol, raloxifene, and bisphenol A decreased IAV titers in hNECs from female, but not male, donors. The estrogenic decrease in viral titer was dependent on the genomic estrogen receptor- 2 (ESR2) as neither genomic ESR1 nor non- genomic GPR30 were expressed in hNEC cultures and addition of the genomic ER antagonist ICI 182,780 reversed the antiviral effects of E2. Treatment of hNECs with E2 had no effect on interferon or chemokine secretion, but significantly downregulated cell metabolic processes, including genes that encode for zinc finger proteins, many of which contain estrogen response elements in their promoters. These data provide novel insights into the cellular and molecular mechanisms of how natural and synthetic estrogens impact IAV infection in respiratory epithelial cells derived from humans.
 
Overall design Primary human nasal epithelial cells from females were exposed to E2 for 24h prior to infection, then infected with an H3N2 strain of influenza a virus for 2 hours. At 24 and 48h post infection, hNECs were collected in Trizol for RNA extraction and hybridization on Affymetrix Human Gene ST 2.0 microarrays.
 
Contributor(s) Peretz J, Pekosz A, Lane AP, Klein SL, Dziedzic A, Jedlicka AE
Citation(s) 26684252
Submission date Nov 19, 2015
Last update date Nov 06, 2022
Contact name Anne E. Jedlicka
Organization name Johns Hopkins University, School of Public Health
Department Molecular Microbiology and Immunology
Lab Genomic Analysis and Sequencing Core
Street address 615 N. Wolfe street
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platforms (1)
GPL16686 [HuGene-2_0-st] Affymetrix Human Gene 2.0 ST Array [transcript (gene) version]
Samples (40)
GSM1945123 hNEC, Vehicle, IAV, 24h, F1
GSM1945124 hNEC, Vehicle, IAV, 24h, F2
GSM1945125 hNEC, Vehicle, IAV, 24h, F3
Relations
BioProject PRJNA302802

Download family Format
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE75208_RAW.tar 307.3 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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