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Do human B-lymphocytes avoid aging until 60 years
A. Knight, P. Nemec, S. Bretzova, L. Valkova, M. Kolmanova, R. Vytopilova, M. Havelka, P. Vsianska, L. Rihova, M. Krejci, M. Piskacek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
NT14310
MZ0
CEP - Centrální evidence projektů
NV15-32935A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
NLK
Free Medical Journals
od 2010
Freely Accessible Journals
od 2010
PubMed Central
od 2010
Europe PubMed Central
od 2010
Open Access Digital Library
od 2010-01-01
- MeSH
- adaptivní imunita genetika imunologie MeSH
- B-lymfocyty imunologie metabolismus MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- přirozená imunita genetika imunologie MeSH
- receptor interleukinu-7 - alfa-podjednotka genetika imunologie metabolismus MeSH
- stanovení celkové genové exprese metody MeSH
- stárnutí genetika imunologie MeSH
- transkriptom genetika imunologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Broad changes in human innate and adaptive immunity are associated with advanced age. The age-related alteration of gene expression was reported for both T and B lymphocytes. We analysed the genome-wide expression profiles (n=20) of naive and whole B cell populations from young and early aged healthy donors under 60 years. We revealed large homogeneity of all analysed genome-wide expression profiles but did not identified any significant gene deregulation between young (30-45 years) and early aged healthy donors (50-60 years). We argue that B cells avoid the aging program on molecular level until 60 years of age. Our results demonstrate the potential of hematopoietic stem cells to generate uncompromised lymphocytes in early elderly. These are very encouraging findings for the general health and the immunity maintenance would not need any intervention to naive B cells. Rather, a suitable immune stimulation in healthy body environment warrants further research into aging of older elderly.
Citace poskytuje Crossref.org
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- $a Knight, Andrea $u Department of Pathological Physiology, Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic. Gamma-Delta T Cell Laboratory, University Hospital Brno, Brno, Czech Republic.
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- $a Broad changes in human innate and adaptive immunity are associated with advanced age. The age-related alteration of gene expression was reported for both T and B lymphocytes. We analysed the genome-wide expression profiles (n=20) of naive and whole B cell populations from young and early aged healthy donors under 60 years. We revealed large homogeneity of all analysed genome-wide expression profiles but did not identified any significant gene deregulation between young (30-45 years) and early aged healthy donors (50-60 years). We argue that B cells avoid the aging program on molecular level until 60 years of age. Our results demonstrate the potential of hematopoietic stem cells to generate uncompromised lymphocytes in early elderly. These are very encouraging findings for the general health and the immunity maintenance would not need any intervention to naive B cells. Rather, a suitable immune stimulation in healthy body environment warrants further research into aging of older elderly.
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