Mitotic clonal expansion: A synchronous process required for adipogenesis

作者：Tang QQ^*; Otto TC; Lane MD

来源：Proceedings of the National Academy of Sciences, 2003, 100(1): 44-49.

DOI：10.1073/pnas.0137044100

• cell cycle
• adipogenesis
• 3T3-L1 preadipocyte
• C/EBP alpha
• PPAR-gamma

When induced to differentiate, growth-arrested 3T3-L1 preadipocytes synchronously reenter the cell cycle and undergo mitotic clonal expansion (MCE) followed by expression of genes that produce the adipocyte phenotype. The preadipocytes traverse the G(1)/S checkpoint synchronously as evidenced by the expression/activation of cdk2-cyclin-E/A, turnover of p27/kip1, hyperphosphorylation of Rb, translocation of cyclin D-1 from nuclei to cytoplasm and GSK-3beta from cytoplasm to nuclei, and incorporation of [H-3]thymidine into DNA. As the cells cross the G(1)/S checkpoint, C/EBPbeta acquires DNA-binding activity, initiating a cascade of transcriptional activation that culminates in the expression of adipocyte proteins. The mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK) inhibitor PD98059 delays, but does not block, MCE and differentiation, the extent of the delay causing a comparable delay in the expression of cell-cycle markers, MCE, and adipogenesis. The more potent and specific MEK inhibitor UO126 and the cyclin-dependent kinase inhibitor roscovitine, which inhibit the cell cycle at different points, block MICE, expression of cell cycle and adipocyte markers, as well as adipogenesis. These results show that MCE is a prerequisite for differentiation of 3T3-L1 preadipocytes into adipocytes.

• 出版日期2003-1-7