Transcriptional regulation of adipogenesis by KLF4

While adipogenesis is known to be controlled by a complex network of transcription factors, less is known about the transcriptional cascade that initiates this process. We report here the characterization of Kruppel-like factor 4 (KLF4) as an essential early regulator of adipogenesis. KIN is expressed in 3T3-L1 cells within 30 min after exposure to a standard adipogenic cocktail of insulin, glucocorticoids, and IBMX. Knockdown of KLF4 inhibits adipogenesis and downregulates C/EBP beta levels. KLF4 binds directly to the C/EBP beta (Cebpb) promoter as shown by chromatin immunoprecipitation and gel shift assays and, together with Krox20, cooperatively trans-activates a C/EBP beta reporter. C/EBP beta knockdown increases levels of KLF4 and Krox20, suggesting that C/EBPP normally suppresses Krox20 and KLF4 expretsion via a tightly controlled negative feedback loop. KLF4 is specifically induced in response to cAMP, which by itself can partially activate adipogenesis. These data suggest that KLF4 functions as an immediate early regulator of adipogenesis to induce C/EBP beta.