The invention relates to the field of the induction of adipocytes, in particular relates to an induced differentiation method of 3T3-L1, and the method comprises the steps of performing
resuscitation, culturing, passage on the 3T3-L1 preadipocytes line until
culture mediums is overgrown with preadipocytes, and after continuously culturing for 36 to 48 hours, adding a
high glucose DMEM culture solution containing an
inducer and 10 percent of fetal calf serum to carry out the induced differentiation for 72 to 96 hours; the
inducer is prepared from 0.9 to 1.1 mu. M of
dexamethasone, 1.0mM of IBMX, and 1.8 to 2.0 mu. M of
insulin; adding the
high glucose DMEM culture solution containing the
insulin and the fetal calf serum to induce continuously for 48 to 96 hours; and then, changing the culture solution once every 48 hours, and
mature adipocytes can be used from the 8th to 10th day after the
inducer is added. The induced differentiation method can shorten the whole induced process of the 3T3-L1 preadipocytes line, the conversion ratio of the adipocytes is stable, and is not influenced by the number of passages and the types of
cell culture dishes, and the error of the conservation rate is within 5%.