Effect of mechanical constriction forces on breast cell lines transcripts
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1034678 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR26635900_1.fastq.gz | Fastqsanger.gz | |||
| SRR26635900_2.fastq.gz | Fastqsanger.gz | |||
| SRR26635901_1.fastq.gz | Fastqsanger.gz | |||
| SRR26635901_2.fastq.gz | Fastqsanger.gz | |||
| SRR26635902_1.fastq.gz | Fastqsanger.gz |
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Project description:Mechanical forces are essential for normal fetal lung development. However, the cellular and molecular mechanisms regulating this process remain largely unknown. In the present study, we used oligonucleotide microarray technology to investigate gene expression profile in cultured E19 rat fetal lung type II epithelial cells exposed to a level of mechanical strain similar to that observed in utero. Significance Analysis of Microarrays (SAM) identified 92 genes differentially expressed by strain. Interestingly, several members of the solute carrier family of amino acid transporters, genes involved in amino acid synthesis and development, and amiloride-sensitive epithelial sodium channel gene were induced by strain. These results were confirmed by quantitative real-time polymerase chain reaction (qRT-PCR). Thus, this study identifies genes induced by strain that may be important for amino acid signaling pathways, protein synthesis and development in fetal type II cells. In addition, these data suggest that mechanical forces may contribute to facilitate lung fluid reabsorption in preparation for birth. Taken together, the present investigation provides further insights into how mechanical forces may modulate fetal lung development. Keywords: lung development, fetal type II epithelial cells, strain response, microarray
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