Temporal correlation of morphological and biochemical changes with the recruitment of different mechanisms of reactive oxygen species formation during human SW872 cell adipogenic differentiation

被引:1
作者
Fiorani, Mara [1 ]
De Matteis, Rita [1 ]
Canonico, Barbara [1 ]
Blandino, Giulia [1 ]
Mazzoli, Alessandro [1 ]
Montanari, Mariele [1 ]
Guidarelli, Andrea [1 ]
Cantoni, Orazio [1 ]
机构
[1] Univ Urbino Carlo Bo, Dept Biomol Sci, Urbino, Italy
关键词
adipocyte differentiation; mitochondria; NADPH oxidase; ROS; OIL RED-O; OXIDATIVE STRESS; GENE-EXPRESSION; PPAR-GAMMA; MITOCHONDRIAL GLUTATHIONE; ADIPOCYTE DIFFERENTIATION; TRANSCRIPTIONAL CONTROL; MICROARRAY ANALYSIS; ROS PRODUCTION; OBESITY;
D O I
10.1002/biof.1769
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human SW872 preadipocyte conversion to mature adipocytes is associated with time-dependent changes in differentiation markers' expression and with morphological changes accompanied by the accumulation of lipid droplets (LDs) as well as by increased mitochondriogenesis and mitochondrial membrane potential. Under identical conditions, the formation of reactive oxygen species (ROS) revealed with a general probe was significant at days 3 and 10 of differentiation and bearly detectable at day 6. NADPH oxidase (NOX)-2 activity determined with an immunocytochemical approach followed a very similar pattern. There was no evidence of mitochondrial ROS (mROS), as detected with a selective fluorescence probe, at days 3 and 6, possibly due to the triggering of the Nrf-2 antioxidant response. mROS were instead clearly detected at day 10, concomitantly with the accumulation of very large LDs, oxidation of both cardiolipin and thioredoxin 2, and decreased mitochondrial glutathione. In conclusion, the morphological and biochemical changes of differentiating SW872 cells are accompanied by the discontinuous formation of ROS derived from NOX-2, increasingly implicated in adipogenesis and adipose tissue dysfunction. In addition, mROS formation was significant only in the late phase of differentiation and was associated with mitochondrial dysfunction.
引用
收藏
页码:837 / 851
页数:15
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