RETRACTED Deficiency of PDK1 in liver results in glucose intolerance, impairment of insulin-regulated gene expression and liver failure

TY - JOUR

T1 - RETRACTED Deficiency of PDK1 in liver results in glucose intolerance, impairment of insulin-regulated gene expression and liver failure

AU - Mora, Alfonso

AU - Lipina, Christopher

AU - Tronche, Francois

AU - Sutherland, Calum

AU - Alessi, Dario R.

N1 - RETRACTED 26 July 2024.

PY - 2005

Y1 - 2005

N2 - The liver plays an important role in insulin-regulated glucose homoeostasis. To study the function of the PDK1 (3-phospho-inositide-dependent protein kinase-1) signalling pathway in mediating insulin's actions in the liver, we employed CRE recombinase/lexP technology to generate L(liver)-PDK1(-1-) mice, which lack expression of PDK1 in hepatocytes and in which insulin failed induce activation of PKB in liver. The L-PDKI-1- mice were not insulin-intolerant, possessed normal levels of blood glucose And insulin under normal feeding conditions, but were markedly,glucose-intolerant when injected with glucose. The L-PDK1 (-1-) mice also possessed 10-fold lower levels of hepatic glycogen compared with control littermates, and were unable to normalize their blood glucose levels within 2 In after injection of insulin. The glucose intolerance of the L-PDK1(-1-) mice may be due to an inability of glucose to suppress hepatic glucose output through the gluconcogenic pathway, since the mRNA encoding hepatic PEPCK (phosphoenolpyruvate carboxykinase), G6Pase (glucose-6-phosphatase) and SREBP1 (sterol-regulatory-element-binding protein 1), which regulate gluconeogenesis, are no longer controlled by feeding. Furthermore, three other insulin-controlled genes, namely IGFBP1 (insulin-like-growth-factor-binding protein-1), IRS2 (insulin receptor substrate 2) and glucokinase, were regulated abnormally by feeding in the liver of PDK1-deficient mice. Finally, the L-PDK1(-1-) mice died between 4-16 weeks of age due to liver failure. These results establish that the PDK1 signalling pathway plays an important role in regulating glucose homoeostasis and controlling expression of insulin-regulated genes. They suggest that a deficiency of the PDK1 pathway in the liver could contribute to development of diabetes, as well as to liver failure.

AB - The liver plays an important role in insulin-regulated glucose homoeostasis. To study the function of the PDK1 (3-phospho-inositide-dependent protein kinase-1) signalling pathway in mediating insulin's actions in the liver, we employed CRE recombinase/lexP technology to generate L(liver)-PDK1(-1-) mice, which lack expression of PDK1 in hepatocytes and in which insulin failed induce activation of PKB in liver. The L-PDKI-1- mice were not insulin-intolerant, possessed normal levels of blood glucose And insulin under normal feeding conditions, but were markedly,glucose-intolerant when injected with glucose. The L-PDK1 (-1-) mice also possessed 10-fold lower levels of hepatic glycogen compared with control littermates, and were unable to normalize their blood glucose levels within 2 In after injection of insulin. The glucose intolerance of the L-PDK1(-1-) mice may be due to an inability of glucose to suppress hepatic glucose output through the gluconcogenic pathway, since the mRNA encoding hepatic PEPCK (phosphoenolpyruvate carboxykinase), G6Pase (glucose-6-phosphatase) and SREBP1 (sterol-regulatory-element-binding protein 1), which regulate gluconeogenesis, are no longer controlled by feeding. Furthermore, three other insulin-controlled genes, namely IGFBP1 (insulin-like-growth-factor-binding protein-1), IRS2 (insulin receptor substrate 2) and glucokinase, were regulated abnormally by feeding in the liver of PDK1-deficient mice. Finally, the L-PDK1(-1-) mice died between 4-16 weeks of age due to liver failure. These results establish that the PDK1 signalling pathway plays an important role in regulating glucose homoeostasis and controlling expression of insulin-regulated genes. They suggest that a deficiency of the PDK1 pathway in the liver could contribute to development of diabetes, as well as to liver failure.

U2 - 10.1042/BJ20041782

DO - 10.1042/BJ20041782

M3 - Article

SN - 0264-6021

VL - 385

SP - 639

EP - 648

JO - Biochemical Journal

JF - Biochemical Journal

IS - 3

ER -