To investigate the differentiation mechanism of grass carp preadipocytes, a primary adipocytes culture system was established. Confluent preadipocytes were induced to differentiation, and the morphology and gene expression were evaluated at different stages. It was shown that preadipocytes were gradually filled with droplets and the cellular lipid content increased during the differentiation. Ultrastructure observation indicated that the number of mitochondria increased with adipocytes differentiation.Consistently, the mitochondrial protein content was elevated in the differentiating adipocytes. q RT-PCR showed that the expression level of lipogenesis-related genes such as peroxisome proliferator activator receptor c(PPAR c),lipoprotein lipase(LPL), fatty acid synthase(FAS) and stearoyl-Co A desaturase(SCD) increased during adipocytes differentiation. The mitochondrial relevant gene also elevated when adipocyte differentiation, such as PPAR coactivator-1(PGC-1 a), PGC-1 b and nuclear respiratory factor(NRF-1). However, the expression of carnitine palmitoyltransferase I a(CPT-1 a) gene decreased at the initial stage, but increased at the last stage of cell differentiation. These results indicated that the differentiation process of grass carp preadipocytes is similar to that of landanimals, but the molecular mechanisms are not exactly the same. The findings revealed in this study provides new information to the study of fish adipocyte differentiation.
Lipophagy is a form of autophagy in mammals.In this cellular process,lipid droplets(LDs)are degraded through the lysosomal degradative pathway[1].During lipophagy,LDs sequestrated in autophagosomes are delivered to lysosomes,which fuse to form autophagosomes and then develop into autophagolysosomes,leading to LDs degradation of[1].A number of studies have demonstrated that lipophagy play important roles in lipid
Jing wangSi-Lan HanLing-Yu LiDong-Liang LuSamwel Mchele LimbuDong-Liang LiMei-Ling ZhangZhen-Yu Du
