2014
DOI: 10.1016/j.diff.2014.06.002
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Autophagy inhibition in early but not in later stages prevents 3T3-L1 differentiation: Effect on mitochondrial remodeling

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Cited by 34 publications
(30 citation statements)
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“…In recent studies, autophagy had been identified as a regulator of cellular differentiation, suggesting that autophagy might regulate the process of adipocytic differentiation [7,8,20]. Through genetic inhibition of critical autophagy-related gene 7 (Atg7), the function of autophagy in regulating adipocytic development was examined by Singh et al and similar results were obtained by Zhang et al [7,8].…”
Section: Discussionsupporting
confidence: 64%
“…In recent studies, autophagy had been identified as a regulator of cellular differentiation, suggesting that autophagy might regulate the process of adipocytic differentiation [7,8,20]. Through genetic inhibition of critical autophagy-related gene 7 (Atg7), the function of autophagy in regulating adipocytic development was examined by Singh et al and similar results were obtained by Zhang et al [7,8].…”
Section: Discussionsupporting
confidence: 64%
“…Skop et al [146] reported that in the first two days, mtDNA copy number declined by 50%, which was followed by a rapid increase and culminated on day 5.After that, mtDNA copy number was moderately reduced to the level observed in preadipocytes [146]. Ryu et al showed that mtDNA copy number started to increase on day 1 and peaked at day 3 during3T3-L1 adipocyte differentiation [149].…”
Section: Mitochondria and Adipocyte Differentiationmentioning
confidence: 95%
“…In preadipocytes, mitochondria are filamentous and organized as continuous reticulum. In contrast, in differentiated adipocytes, they are fragmented, punctual and redistributed around lipid droplets [146]. Mitochondrial fusion and fission have direct influence on lipid accumulation in adipocytes.…”
Section: Mitochondria and Adipocyte Differentiationmentioning
confidence: 96%
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“…Differentiation of the mouse 3T3-L1 preadipocyte cell line was performed according to Skop et al (2014). Briefly, the cells were grown to confluence in DMEM (Sigma-Aldrich) supplemented with 10% FBS (Sigma Aldrich) in 5% CO 2 atmosphere at 37°C.…”
Section: Analysis Of M × Paradisiaca Extractsmentioning
confidence: 99%