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Series GSE255744 Query DataSets for GSE255744
Status Public on May 01, 2024
Title Se Deficiency Exacerbates Hyperoxia-Induced Lung Injury in Newborn C3H/HeN Mice
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Extremely preterm infants are often treated with supraphysiological oxygen which contributes to the development of bronchopulmonary dysplasia (BPD). These same infants exhibit compromised antioxidant capacities due in part to selenium (Se) deficiency. The present study was designed to develop a perinatal Se deficiency mouse model, identify the effects of newborn hyperoxia exposure, and explore alternative pathways affected by Se deficiency (SeD) that would contribute to impaired lung development. Se deficient breeding pairs were generated, once pups were born, they were exposed to room air or 85% O2 for 14 d. Survival, antioxidant and Nrf2-regulated protein expression, and RNA seq analyses were performed. Greater than 40% mortality was observed in Se deficient (SeD), hyperoxia exposed pups. Surviving SeD pups had greater lung growth deficits than Se sufficient (SeS) pups exposed to hyperoxia. Gpx2 and 4 protein and Gpx activity were significantly decreased in SeD pups. Nrf2-regulated proteins, NQO1 and Gclc were increased in the setting of Se deficiency and hyperoxia exposure. RNA seq revealed significant decreases in the Wnt/-catenin and Notch pathways. Se is a biologically relevant modulator of perinatal lung development and antioxidant responses, especially in the context of hyperoxia exposure. RNA seq implicates pathways essential for normal lung development are dysregulated by Se deficiency.
 
Overall design Male and female C3H/HeN mice were placed on diets that differ only in Se content (Se-sufficient (SeS) with 0.4 ppm or Se-deficient (SeD) containing <0.01 ppm sodium selenite) at 3 weeks of life and remained on the diets throughout the experiment.
After 3 weeks on respective SeS or SeD diets, mice were bred to create SeS and SeD litters for use in the present studies.
At birth, pups were placed in FiO2 0.85 hyperoxia or remained in room air. Pups were euthanized at PN1 or 3 and lungs were perfused with ice-cold PBS, snap-frozen in Trizol, and stored at –80°C for RNAseq.
 
Contributor(s) Bailey-Downs LC, Sherlock L, Crossley MN, Rivera Negron A, Pierce PT, Wang S, Zhong H, Carter C, Burge K, Eckert J, Rogers LK, Vitiello PF, Tipple TE
Citation(s) 38671839
Submission date Feb 13, 2024
Last update date May 01, 2024
Contact name Trent E Tipple
Organization name University of Oklahoma Health Sciences Center
Department Pediatrics
Lab Center for Pregnancy & Newborn Health
Street address 800 Research Pkwy
City Oklahoma City
State/province Oklahoma
ZIP/Postal code 73104
Country USA
 
Platforms (1)
GPL30172 NextSeq 2000 (Mus musculus)
Samples (24)
GSM8078846 SeS, hyperoxia, PN1, Replicate 1
GSM8078847 SeS, hyperoxia, PN1, Replicate 2
GSM8078848 SeD, Room Air, PN1, Replicate 1
Relations
BioProject PRJNA1076259

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Supplementary file Size Download File type/resource
GSE255744_gene_expression.xlsx 40.0 Mb (ftp)(http) XLSX
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Raw data are available in SRA
Processed data are available on Series record

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