J Clin Invest 2012,
Ai, Ding; Chen, Chiyuan; Han, Seongah; Ganda, Anjali; Murphy, Andrew J; Haeusler, Rebecca; Thorp, Edward; Accili, Domenico; Horton, Jay D; Tall, Alan R
Individuals with type 2 diabetes have an increased risk of atherosclerosis. One factor underlying this is dyslipidemia, which in hyperinsulinemic subjects with early type 2 diabetes is typically characterized by increased VLDL secretion but normal LDL cholesterol levels, possibly reflecting enhanced catabolism of LDL via hepatic LDLRs. Recent studies have also suggested that hepatic insulin signaling sustains LDLR levels. We therefore sought to elucidate the mechanisms linking hepatic insulin signaling to regulation of LDLR levels. In WT mice, insulin receptor knockdown by shRNA resulted in decreased hepatic mTORC1 signaling and LDLR protein levels. It also led to increased expression of PCSK9, a known post-transcriptional regulator of LDLR expression. Administration of the mTORC1 inhibitor rapamycin caused increased expression of PCSK9, decreased levels of hepatic LDLR protein, and increased levels of VLDL/LDL cholesterol in WT but not Pcsk9-/- mice. Conversely, mice with increased hepatic mTORC1 activity exhibited decreased expression of PCSK9 and increased levels of hepatic LDLR protein levels. Pcsk9 is regulated by the transcription factor HNF1α, and our further detailed analyses suggest that increased mTORC1 activity leads to activation of PKCδ, reduced activity of HNF4α and HNF1α, decreased PCSK9 expression, and ultimately increased hepatic LDLR protein levels, which result in decreased circulating LDL levels. We therefore suggest that PCSK9 inhibition could be an effective way to reduce the adverse side effect of increased LDL levels that is observed in transplant patients taking rapamycin as immunosuppressive therapy.
Diseases/Pathways annotated by Medline MESH:
Hyperinsulinism, Insulin Resistance, Postoperative Complications
Document information provided by NCBI PubMed
Text Mining Data
LDL — PCSK9: " Regulation
of hepatic LDL
receptors by mTORC1 and PCSK9
in mice "
LDL — mTORC1: " Regulation of hepatic LDL receptors by mTORC1 and PCSK9 in mice "
LDLR → mTORC1: " Pcsk9 is regulated by the transcription factor HNF1a, and our further detailed analyses suggest that increased mTORC1 activity leads to activation of PKCd, reduced activity of HNF4a and HNF1a, decreased PCSK9 expression, and ultimately increased hepatic LDLR protein levels, which result in decreased circulating LDL levels "
Manually curated Databases
No curated data.