http://www.cnr.it/ontology/cnr/individuo/prodotto/ID5283
In vitro apoptotic cell death during erythroid differentiation, (Articolo in rivista)
- Type
- Label
- In vitro apoptotic cell death during erythroid differentiation, (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1023/B:APPT.0000018805.63663.a5 (literal)
- Alternative label
L. ZAMAI, S. BURATTINI, F. LUCHETTI, B. CANONICO, P. FERRI, E. MELLONI, A. GONELLI, L. GUIDOTTI, S. PAPA, E. FALCIERI, (2004)
In vitro apoptotic cell death during erythroid differentiation,
in Apoptosis (Lond.)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- L. ZAMAI, S. BURATTINI, F. LUCHETTI, B. CANONICO, P. FERRI, E. MELLONI, A. GONELLI, L. GUIDOTTI, S. PAPA, E. FALCIERI, (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Titolo
- In vitro apoptotic cell death during erythroid differentiation, (literal)
- Abstract
- Erythropoiesis occurs in bone marrow and it has been
shown that during in vivo erythroid differentiation some
immature erythroblasts undergo apoptosis. In this regard,
it is known that immature erythroblasts are FasLand
TRAIL-sensitive and can be killed by cells expressing
these ligand molecules. In the present study, we have investigated
the cell death phenomenon that occurs during
a common unilineage model of erythroid development.
Purified CD34+human haemopoietic progenitors were
cultured in vitro in the presence of SCF, IL-3 and erythropoietin.
Their differentiation stages and apoptosis were
followed by multiple technical approaches.
Flow cytometric evaluation of surface and intracellular
molecules revealed that glycophorin A appeared at
day 3-4 of incubation and about 75% of viable cells coexpressed
high density glycophorin A (Glybright) and adult
haemoglobin at day 14 of culture, indicating that this
system reasonably recapitulates in vivo normal erythropoiesis.
Interestingly, when mature (Glybright) erythroid
cells reached their higher percentages (day 14) almost
half of cultured cells were apoptotic. Morphological studies
indicated that the majority of dead cells contained cytoplasmic
granular material typical of basophilic stage,
and DNA analysis by flow cytometry and TUNEL reaction
revealed nuclear fragmentation.
These observations indicate that in vitro unilineage
erythroid differentiation, as in vivo, is associated with
apoptotic cell death of cells with characteristics of
basophilic erythroblasts. We suggest that the interactions
between different death receptors on immature basophilic
erythroblasts with their ligands on more mature
erythroblasts may contribute to induce apoptosis in vitro. (literal)
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