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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.
Language English Country Germany
Grant support
NR8233
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
SpringerLink Journals
from 2005-01-01 to 2008-12-31
ProQuest Central
from 1997-01-01 to 2017-12-31
Medline Complete (EBSCOhost)
from 2000-01-01 to 1 year ago
Nursing & Allied Health Database (ProQuest)
from 1997-01-01 to 2017-12-31
Health & Medicine (ProQuest)
from 1997-01-01 to 2017-12-31
Public Health Database (ProQuest)
from 1997-01-01 to 2017-12-31
- MeSH
- Silver Staining MeSH
- Cell Nucleolus metabolism MeSH
- Cell Cycle physiology MeSH
- K562 Cells MeSH
- Bone Marrow Cells metabolism MeSH
- DNA, Neoplasm metabolism MeSH
- Financing, Organized MeSH
- Granulocytes metabolism ultrastructure MeSH
- HL-60 Cells MeSH
- Leukemia metabolism MeSH
- Humans MeSH
- Nucleolus Organizer Region metabolism MeSH
- Plasma Cells metabolism ultrastructure MeSH
- RNA, Neoplasm metabolism MeSH
- Cellular Senescence physiology MeSH
- Protein Transport MeSH
- Check Tag
- Humans 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.
References provided by Crossref.org
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- $a 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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