Differential activation of peroxisome proliferator-activated receptor-gamma by troglitazone and rosiglitazone.

HS Camp, O Li, SC Wise, YH Hong, CL Frankowski… - Diabetes, 2000 - Am Diabetes Assoc
HS Camp, O Li, SC Wise, YH Hong, CL Frankowski, X Shen, R Vanbogelen, T Leff
Diabetes, 2000Am Diabetes Assoc
The antidiabetic thiazolidinediones, which include troglitazone and rosiglitazone, are
ligands for the nuclear receptor peroxisome proliferator-activated receptor (PPAR)-gamma
and exert their antihyperglycemic effects by regulation of PPAR-gamma-responsive genes.
We report here that PPAR-gamma activation by troglitazone depends on the experimental
setting. Troglitazone acts as a partial agonist for PPAR-gamma in transfected muscle
(C2C12) and kidney (HEK 293T) cells, producing a submaximal transcriptional response …
The antidiabetic thiazolidinediones, which include troglitazone and rosiglitazone, are ligands for the nuclear receptor peroxisome proliferator-activated receptor (PPAR)-gamma and exert their antihyperglycemic effects by regulation of PPAR-gamma-responsive genes. We report here that PPAR-gamma activation by troglitazone depends on the experimental setting. Troglitazone acts as a partial agonist for PPAR-gamma in transfected muscle (C2C12) and kidney (HEK 293T) cells, producing a submaximal transcriptional response (1.8- to 2.5-fold activation) compared with rosiglitazone (7.4- to 13-fold activation). Additionally, troglitazone antagonizes rosiglitazone-stimulated PPAR-gamma transcriptional activity. Limited protease digestion of PPAR-gamma suggests conformational differences in the receptor bound to troglitazone versus rosiglitazone. Consistent with this finding, an in vitro coactivator association assay demonstrated that troglitazone-bound PPAR-gamma recruited the transcriptional coactivators p300 and steroid receptor coactivator 1 less efficiently than rosiglitazone-bound receptor. In contrast to these observations, troglitazone behaves as a full agonist of PPAR-gamma in 3T3L1 adipocytes. Two-dimensional protein gel electrophoresis demonstrated that troglitazone and rosiglitazone regulated distinct but overlapping sets of genes in several cell types. Thus, troglitazone may behave as a partial agonist under certain physiological circumstances and as a full agonist in others. These differences could be caused by variations in the amount of specific cofactors, differences in PPAR response elements, or the presence of different isoforms of PPAR-gamma.
Am Diabetes Assoc