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| Status |
Public on Dec 09, 2011 |
| Title |
Sarcolipin is a potential biomarker for dystrophy and is involved in inflammatory processes in skeletal muscles |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by array
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| Summary |
Myopathies and muscular dystrophies are devastating diseases sharing characteristic symp-toms. Little is known about common aetiopathology and biomarkers are rare. We studied skeletal muscle gene expression in mouse models of myopathies. As dystrophic processes in muscles are characterised by inflammatory processes, we expanded our analy-sis on a rat model of sepsis. We find 25 commonly dysregulated genes. Sarcolipin was upregulated most, exhibiting in-creased protein levels in different muscles as well as in rats treated with an inflammatory agent. Upregulation strongly correlated with disease status. Our findings suggest Sarcolipin as a potential biomarker and imply a new function in inflam-matory response.
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| Overall design |
Comparison of the expression profile of quadriceps in 2 B6C3Fe a/a-Ttnmdm/J mice with Titin-mutation versus the expression profile of 2 mice without the mutation in Titin [Ttn].
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| Contributor(s) |
Kohl CH, Sticht C, Tsagogiorgas C, Labeit D, Witt CC |
| Citation missing |
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| Submission date |
Oct 21, 2011 |
| Last update date |
Jun 21, 2012 |
| Contact name |
Carsten Sticht |
| Organization name |
University Heidelberg
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| Department |
ZMF
|
| Street address |
Theodor-Kutzer-Ufer
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| City |
Mannheim |
| ZIP/Postal code |
68169 |
| Country |
Germany |
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| Platforms (1) |
| GPL14661 |
[Mouse430_2_Mm_EntrezG] Affymetrix GeneChip Mouse Genome 430 2.0 Array [Brainarray Version 13] |
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| Samples (4)
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| Relations |
| BioProject |
PRJNA149181 |
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