Elevated mouse hepatic betatrophin expression does not increase human β-cell replication in the transplant setting

Y Jiao, J Le Lay, M Yu, A Naji, KH Kaestner - Diabetes, 2014 - Am Diabetes Assoc
Y Jiao, J Le Lay, M Yu, A Naji, KH Kaestner
Diabetes, 2014Am Diabetes Assoc
The recent discovery of betatrophin, a protein secreted by the liver and white adipose tissue
in conditions of insulin resistance and shown to dramatically stimulate replication of mouse
insulin-producing β-cells, has raised high hopes for the rapid development of a novel
therapeutic approach for the treatment of diabetes. At present, however, the effects of
betatrophin on human β-cells are not known. Here we use administration of the insulin
receptor antagonist S961, shown to increase betatrophin gene expression and stimulate β …
The recent discovery of betatrophin, a protein secreted by the liver and white adipose tissue in conditions of insulin resistance and shown to dramatically stimulate replication of mouse insulin-producing β-cells, has raised high hopes for the rapid development of a novel therapeutic approach for the treatment of diabetes. At present, however, the effects of betatrophin on human β-cells are not known. Here we use administration of the insulin receptor antagonist S961, shown to increase betatrophin gene expression and stimulate β-cell replication in mice, to test its effect on human β-cells. Although mouse β-cells, in their normal location in the pancreas or when transplanted under the kidney capsule, respond with a dramatic increase in β-cell DNA replication, human β-cells are completely unresponsive. These results put into question whether betatrophin can be developed as a therapeutic approach for treating human diabetes.
Am Diabetes Assoc