http://www.cnr.it/ontology/cnr/individuo/prodotto/ID180267
Erythropoietin enhances cell proliferation and survival of human fetal neuronal progenitors in normoxia (Articolo in rivista)
- Type
- Label
- Erythropoietin enhances cell proliferation and survival of human fetal neuronal progenitors in normoxia (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.brainres.2012.02.043 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Sanja Pavlicaa; Javorina Milosevic; Mario Keller; Mattes Schulze; Frank Peinemann; Antonella Piscioneri; Loredana De Bartolo; Kai Darsow; Sebastian Bartel; Harald A. Lange; Augustinus Bader (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.sciencedirect.com/science/article/pii/S0006899312003496 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Cell Technologies and Applied Stem Cell Biology, Biomedical-Biotechnological Centre, University of Leipzig, Leipzig, Germany
Translational Centre for Regenerative Medicine-Leipzig (TRM-Leipzig), University of Leipzig, Germany
Institute of Bioprocess Engineering, Friedrich-Alexander University Erlangen-Nuremberg (FAU), Erlangen, Germany
Institute on Membrane Technology, National Research Council of Italy, c/o University of Calabria (ITM-CNR), Rende, Italy (literal)
- Titolo
- Erythropoietin enhances cell proliferation and survival of human fetal neuronal progenitors in normoxia (literal)
- Abstract
- Extensive data reporting the neurogenerative, neuroprotective and neuroregenerative
potential of erythropoietin (EPO), mainly on RNA level, can be found in the literature.
However, there is still a poor knowledge on the response of neuronal progenitor cells
(NPC) upon stimulation with EPO in terms of the protein species involved. Herein, the effect
of EPO on the proliferation of human mesencephalic NPC (hmNPC) under normoxia
is monitored using cellular assays and proteomic analysis (two-dimensional gel electrophoresis
and MALDI-TOF mass spectrometry). The administration of EPO increased the
proliferation of hmNPC within 4 days after application. It positively influenced the cellcycle
progression by affecting the G2 phase of the cell cycle. A proteomic analysis of
the protein expression in hmNPC cultures 4 days after EPO treatment identified 8 proteins
differentially expressed in EPO-treated cultures. It is likely that one or more of the identified
proteins are involved in cellular pathways that promote cell proliferation and differentiation
of hmNPC under normoxia. Their further characterization could provide
cellular targets for the development of new therapeutic agents to treat CNS injury. Moreover,
as EPO signaling is hypoxia-inducible, our findings may also indicate the beneficial
effect of EPO to mimic hypoxia, while bypassing its negative effects, to culture human
fetal midbrain-derived progenitor cells. (literal)
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