α-Tocopherol Acetate Attenuates Mitochondrial Oxygen Consumption and Maintains Primitive Cells within Mesenchymal Stromal Cell Population
Author(s) -
Darija Loncaric,
Laura Rodríguez,
Christelle Debeissat,
Nicolas Touya,
Véronique Labat,
Arnaud Villacreces,
AnneKarine BouzierSore,
JeanMax Pasquet,
Philippe Brunet de la Grange,
Marija VlaskiLafarge,
Sonja Pavlović,
Zoran Ivanović
Publication year - 2021
Publication title -
stem cell reviews and reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.247
H-Index - 73
eISSN - 2629-3269
pISSN - 2629-3277
DOI - 10.1007/s12015-020-10111-9
Subject(s) - mesenchymal stem cell , stromal cell , population , microbiology and biotechnology , chemistry , stem cell , progenitor cell , vitamin e , alpha tocopherol , mitochondrion , biology , biochemistry , cancer research , medicine , antioxidant , environmental health
We present here the data showing, in standard cultures exposed to atmospheric O 2 concentration, that alpha-tocopherol acetate (α-TOA) has a positive impact on primitive cells inside mesenchymal stromal cell (MstroC) population, by maintaining their proliferative capacity. α-TOA decreases the O 2 consumption rate of MStroC probably by impacting respiratory chain complex II activity. This action, however, is not associated with a compensatory increase in glycolysis activity, in spite of the fact that the degradation of HIF-1α was decreased in presence of α-TOA. This is in line with a moderate enhancement of mtROS upon α-TOA treatment. However, the absence of glycolysis stimulation implies the inactivity of HIF-1α which might - if it were active - be related to the maintenance of stemness. It should be stressed that α-TOA might act directly on the gene expression as well as the mtROS themselves, which remains to be elucidated. Alpha-tocopherol acetate (α-TOA), a synthetic vitamin E ester, attenuates electron flow through electron transport chain (ETC) which is probably associated with a moderate increase in mtROS in Mesenchymal Stromal Cells. α-TOA action results in enhancement of the proliferative capacity and maintenance of the differentiation potential of the mesenchymal stem and progenitor cells.
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