id paper:paper_17590914_v5_n1_p43_Silvestroff
record_format dspace
spelling paper:paper_17590914_v5_n1_p43_Silvestroff2023-06-08T16:29:01Z Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation Nerve/glia antigen 2 (NG2) Oligodendrocyte Platelet-derived growth factor receptor α (PDGFRα) Progenitor Proliferation Transferrin apotransferrin ferric ion glial fibrillary acidic protein nestin oligodendrocyte transcription factor 2 platelet derived growth factor alpha receptor transcription factor Sox2 transferrin animal cell animal cell culture animal experiment animal tissue article cell proliferation controlled study culture medium DNA content female immunocytochemistry immunohistochemistry in vitro study male neural stem cell neuroblast newborn nonhuman oligodendroglia protein expression rat subventricular zone Western blotting NSC (neural stem cells)/NPC (neural progenitor cells) are multipotent and self-renew throughout adulthood in the SVZ (subventricular zone) of the mammalian CNS (central nervous system). These cells are considered interesting targets for CNS neurodegenerative disorder cell therapies, and understanding their behaviour in vitro is crucial if they are to be cultured prior to transplantation. We cultured the SVZ tissue belonging to newborn rats under the form of NS (neurospheres) to evaluate the effects of Tf (transferrin) on cell proliferation. The NS were heterogeneous in terms of the NSC/NPC markers GFAP (glial fibrillary acidic protein), Nestin and Sox2 and the OL (oligodendrocyte) progenitor markers NG2 (nerve/glia antigen 2) and PDGFRα (platelet-derived growth factor receptor α). The results of this study indicate that aTf (apoTransferrin) is able to increase cell proliferation of SVZ-derived cells in vitro, and that these effects were mediated at least in part by the TfRc1 (Tf receptor 1). Since OPCs (oligodendrocyte progenitor cells) represent a significant proportion of the proliferating cells in the SVZ-derived primary cultures, we used the immature OL cell line N20.1 to show that Tf was able to augment the proliferation rate of OPC, either by adding aTf to the culture medium or by overexpressing rat Tf in situ. The culture medium supplemented with ferric iron, together with aTf, increased the DNA content, while ferrous iron did not. The present work provides data that could have a potential application in human cell replacement therapies for neurodegenerative disease and/or CNS injury that require the use of in vitro amplified NPCs. © 2013 The Author(s). 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_17590914_v5_n1_p43_Silvestroff http://hdl.handle.net/20.500.12110/paper_17590914_v5_n1_p43_Silvestroff
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Nerve/glia antigen 2 (NG2)
Oligodendrocyte
Platelet-derived growth factor receptor α (PDGFRα)
Progenitor
Proliferation
Transferrin
apotransferrin
ferric ion
glial fibrillary acidic protein
nestin
oligodendrocyte transcription factor 2
platelet derived growth factor alpha receptor
transcription factor Sox2
transferrin
animal cell
animal cell culture
animal experiment
animal tissue
article
cell proliferation
controlled study
culture medium
DNA content
female
immunocytochemistry
immunohistochemistry
in vitro study
male
neural stem cell
neuroblast
newborn
nonhuman
oligodendroglia
protein expression
rat
subventricular zone
Western blotting
spellingShingle Nerve/glia antigen 2 (NG2)
Oligodendrocyte
Platelet-derived growth factor receptor α (PDGFRα)
Progenitor
Proliferation
Transferrin
apotransferrin
ferric ion
glial fibrillary acidic protein
nestin
oligodendrocyte transcription factor 2
platelet derived growth factor alpha receptor
transcription factor Sox2
transferrin
animal cell
animal cell culture
animal experiment
animal tissue
article
cell proliferation
controlled study
culture medium
DNA content
female
immunocytochemistry
immunohistochemistry
in vitro study
male
neural stem cell
neuroblast
newborn
nonhuman
oligodendroglia
protein expression
rat
subventricular zone
Western blotting
Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
topic_facet Nerve/glia antigen 2 (NG2)
Oligodendrocyte
Platelet-derived growth factor receptor α (PDGFRα)
Progenitor
Proliferation
Transferrin
apotransferrin
ferric ion
glial fibrillary acidic protein
nestin
oligodendrocyte transcription factor 2
platelet derived growth factor alpha receptor
transcription factor Sox2
transferrin
animal cell
animal cell culture
animal experiment
animal tissue
article
cell proliferation
controlled study
culture medium
DNA content
female
immunocytochemistry
immunohistochemistry
in vitro study
male
neural stem cell
neuroblast
newborn
nonhuman
oligodendroglia
protein expression
rat
subventricular zone
Western blotting
description NSC (neural stem cells)/NPC (neural progenitor cells) are multipotent and self-renew throughout adulthood in the SVZ (subventricular zone) of the mammalian CNS (central nervous system). These cells are considered interesting targets for CNS neurodegenerative disorder cell therapies, and understanding their behaviour in vitro is crucial if they are to be cultured prior to transplantation. We cultured the SVZ tissue belonging to newborn rats under the form of NS (neurospheres) to evaluate the effects of Tf (transferrin) on cell proliferation. The NS were heterogeneous in terms of the NSC/NPC markers GFAP (glial fibrillary acidic protein), Nestin and Sox2 and the OL (oligodendrocyte) progenitor markers NG2 (nerve/glia antigen 2) and PDGFRα (platelet-derived growth factor receptor α). The results of this study indicate that aTf (apoTransferrin) is able to increase cell proliferation of SVZ-derived cells in vitro, and that these effects were mediated at least in part by the TfRc1 (Tf receptor 1). Since OPCs (oligodendrocyte progenitor cells) represent a significant proportion of the proliferating cells in the SVZ-derived primary cultures, we used the immature OL cell line N20.1 to show that Tf was able to augment the proliferation rate of OPC, either by adding aTf to the culture medium or by overexpressing rat Tf in situ. The culture medium supplemented with ferric iron, together with aTf, increased the DNA content, while ferrous iron did not. The present work provides data that could have a potential application in human cell replacement therapies for neurodegenerative disease and/or CNS injury that require the use of in vitro amplified NPCs. © 2013 The Author(s).
title Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
title_short Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
title_full Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
title_fullStr Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
title_full_unstemmed Neural and oligodendrocyte progenitor cells: Transferrin effects on cell proliferation
title_sort neural and oligodendrocyte progenitor cells: transferrin effects on cell proliferation
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_17590914_v5_n1_p43_Silvestroff
http://hdl.handle.net/20.500.12110/paper_17590914_v5_n1_p43_Silvestroff
_version_ 1768544294005637120