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To the intranucleolar translocation of AgNORs in leukemic early granulocytic and plasmacytic precursors
Smetana K., Klamová H., Pluskalová M., Stöckbauer P., Hrkal Z.
Jazyk angličtina Země Německo
Grantová podpora
NR8233
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Část
Zdroj
NLK
SpringerLink Journals
od 2005-01-01 do 2008-12-31
ProQuest Central
od 1997-01-01 do 2017-12-31
Medline Complete (EBSCOhost)
od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
Health & Medicine (ProQuest)
od 1997-01-01 do 2017-12-31
Public Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
- MeSH
- barvení stříbrem MeSH
- buněčné jadérko metabolismus MeSH
- buněčný cyklus fyziologie MeSH
- buňky K562 MeSH
- buňky kostní dřeně metabolismus MeSH
- DNA nádorová metabolismus MeSH
- financování organizované MeSH
- granulocyty metabolismus ultrastruktura MeSH
- HL-60 buňky MeSH
- leukemie metabolismus MeSH
- lidé MeSH
- organizátor jadérka metabolismus MeSH
- plazmatické buňky metabolismus ultrastruktura MeSH
- RNA nádorová metabolismus MeSH
- stárnutí buněk fyziologie MeSH
- transport proteinů MeSH
- Check Tag
- lidé MeSH
Early leukemic granulocytic and plasmacytic precursors were studied in vitro and in vivo to provide an information on the intranucleolar distribution of AgNORs (silver stained nucleolus organizer regions). In most of these cells AgNORs appeared as clusters of silver stained particles distributed in the whole nucleolar body. On the other hand, in some leukemic early granulocytic precursors, i.e., in myeloblasts and promyelocytes enlarged AgNORs were translocated in the nucleolar peripheral part. In addition, the number of translocated AgNORs at the nucleolar periphery was significantly smaller. Such translocation of a reduced number of AgNORs was easily produced by experimental aging, i.e., starving of cultured leukemic early granulocytic precursors (HL-60 and K562 cells) in vitro and seems to be reversible. Similar translocation of a reduced number of AgNORs was also produced by aging of leukemic plasmacytic precursors. Thus, the translocation of the reduced number of AgNORs to the nucleolar periphery in some blastic leukemic hematopoietic cells might be an useful marker of their aging at the single cell level. However, more studies in this direction are required in the future.
Citace poskytuje Crossref.org
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