Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of mouse ob/ob leptin-treated and ob/ob saline-treated lungs.


ABSTRACT: We hypothesize that gene expression in the lungs of these differentially-treated mice are divergent thus contributing to the disparity in their phenotypes. More specifically, (1) Effects of Leptin-treatment of ob/ob postnatal mice lungs are known to be volume-dependent from 2 to 10 wks of age, and are independent of the hypometabolism associated with leptin deficiency. ; (2) Leptin is critical to postnatal lung remodeling, particularly related to enlarged alveolar surface area. In order to test these hypotheses at the gene expression level, we utilized microarray analysis to examine transcriptional differences between lungs of leptin or saline-treated ob/ob postnatal mice. Experiment Overall Design: This study utilizes microarray analysis to test these hypotheses. Three sets of lungs were harvested from both treatments (Leptin or Saline) at around 1 mo. postnatal. RNA was isolated and used for global gene expression profiling (Affymetrix Mouse 430A array). Statistically significant gene expression was determined as a minimum 6 counts of 9 pairwise comparisons, minimum 1.5-fold change, and p < 0.05.

ORGANISM(S): Mus musculus

SUBMITTER: vikas misra 

PROVIDER: E-GEOD-10915 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Effects of leptin deficiency on postnatal lung development in mice.

Huang Kewu K   Rabold Richard R   Abston Eric E   Schofield Brian B   Misra Vikas V   Galdzicka Ewa E   Lee Hannah H   Biswal Shyam S   Mitzner Wayne W   Tankersley Clarke G CG  

Journal of applied physiology (Bethesda, Md. : 1985) 20080508 1


Leptin modulates energy metabolism and lung development. We hypothesize that the effects of leptin on postnatal lung development are volume dependent from 2 to 10 wk of age and are independent of hypometabolism associated with leptin deficiency. To test the hypotheses, effects of leptin deficiency on lung maturation were characterized in age groups of C57BL/6J mice with varying Lep(ob) genotypes. Quasi-static pressure-volume curves and respiratory impedance measurements were performed to profile  ...[more]

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