MicroRNA let-7 Regulates 3T3-L1 Adipogenesis
Author(s) -
Tingwan Sun,
Mingui Fu,
Angie L. Bookout,
Steven A. Kliewer,
David J. Mangelsdorf
Publication year - 2009
Publication title -
molecular endocrinology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/me.2008-0298
Subject(s) - adipogenesis , biology , gene knockdown , microrna , microbiology and biotechnology , hmga2 , cellular differentiation , 3t3 l1 , 3t3 cells , transcription factor , ectopic expression , cell culture , gene , transfection , genetics , mesenchymal stem cell
Differentiation of 3T3-L1 cells into adipocytes involves a highly orchestrated series of events including clonal expansion, growth arrest, and terminal differentiation. The mechanisms coordinating these different steps are not yet fully understood. Here we investigated whether microRNAs (miRNAs) play a role in this process. Microarray analysis was performed to detect miRNA expression during 3T3-L1 preadipocyte differentiation. Several miRNAs, including let-7, were up-regulated during 3T3-L1 adipogenesis. Ectopic introduction of let-7 into 3T3-L1 cells inhibited clonal expansion as well as terminal differentiation. The mRNA encoding high-mobility group AT-hook 2 (HMGA2), a transcription factor that regulates growth and proliferation in other contexts, was inversely correlated with let-7 levels during 3T3-L1 cell adipogenesis, and let-7 markedly reduced HMGA2 concentrations. Knockdown of HMGA2 inhibited 3T3-L1 differentiation. These results suggest that let-7 plays an important role in adipocyte differentiation and that it does so in part by targeting HMGA2, thereby regulating the transition from clonal expansion to terminal differentiation.
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