Transcriptome temporal and functional analysis of liver regeneration termination
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23130906
DOI
10.33549/physiolres.932393
PII: 932393
Knihovny.cz E-zdroje
- MeSH
- genetická transkripce MeSH
- hepatektomie MeSH
- játra metabolismus MeSH
- krysa rodu Rattus MeSH
- metabolismus lipidů genetika MeSH
- modely nemocí na zvířatech MeSH
- nemoci jater genetika metabolismus veterinární MeSH
- potkani Wistar MeSH
- receptory aktivované proliferátory peroxizomů metabolismus MeSH
- regenerace jater genetika MeSH
- regulace genové exprese MeSH
- transkriptom * MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- receptory aktivované proliferátory peroxizomů MeSH
Decades of liver regeneration studies still left the termination phase least elucidated. However regeneration ending mechanisms are clinicaly relevant. We aimed to analyse the timing and transcriptional control of the latest phase of liver regeneration, both controversial. Male Wistar rats were subjected to 2/3 partial hepatectomy with recovery lasting from 1 to 14 days. Time-series microarray data were assessed by innovative combination of hierarchical clustering and principal component analysis and validated by real-time RT-PCR. Hierarchical clustering and principal component analysis in agreement distinguished three temporal phases of liver regeneration. We found 359 genes specifically altered during late phase regeneration. Gene enrichment analysis and manual review of microarray data suggested five pathways worth further study: PPAR signalling pathway; lipid metabolism; complement, coagulation and fibrinolytic cascades; ECM remodelling and xenobiotic biotransformation. Microarray findings pertinent for termination phase were substantiated by real-time RT-PCR. In conclusion, transcriptional profiling mapped late phase of liver regeneration beyond 5(th) day of recovery and revealed 5 pathways specifically acting at this time. Inclusion of longer post-surgery intervals brought improved coverage of regeneration time dynamics and is advisable for further works. Investigation into the workings of suggested pathways might prove helpful in preventing and managing liver tumours.
Citace poskytuje Crossref.org