Ontology highlight
ABSTRACT:
PROVIDER: PRJEB12959 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| ERR1306550.fastq.gz | Fastqsanger.gz | |||
| ERR1306560.fastq.gz | Fastqsanger.gz | |||
| ERR1306570.fastq.gz | Fastqsanger.gz | |||
| ERR1306580.fastq.gz | Fastqsanger.gz | |||
| ERR1306850_1.fastq.gz | Fastqsanger.gz |
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2017-09-19 | E-MTAB-5101 | biostudies-arrayexpress
Project description:The macrolide rapamycin is known for its immunosuppressive properties since it inhibits mTOR (mammalian target of rapamycin), which activity affects differentiation and functions of various innate and adaptive immune cells involved in graft-versus-host disease development. Since rapamycin procures immunosuppressive effects on the immune response, rapamycin is an attractive candidate for graft-versus-host disease prevention after allogeneic bone marrow transplantation We used an MHC class I and II mismatched parent into F1 bone marrow transplantation mouse model to elucidate the mechanisms of rapamycin on T cells in the context of graft-versus-host disease prevention. To define the impact of rapamycin therapy on T cells gene expression profile, we performed mircoarray analysis and compared gene expression profiles of sorted splenic T cells from rapamycin and PBS treated mice
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