To the intranucleolar translocation of AgNORs in leukemic early granulocytic and plasmacytic precursors
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- barvení stříbrem MeSH
- buněčné jadérko metabolismus MeSH
- buněčný cyklus fyziologie MeSH
- buňky K562 MeSH
- buňky kostní dřeně metabolismus MeSH
- DNA nádorová metabolismus 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
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA nádorová MeSH
- RNA nádorová 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.
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