PC-1 content in skeletal muscle of non-obese, non-diabetic subjects: relationship to insulin receptor tyrosine kinase and whole body insulin sensitivity
- PMID: 8897006
- DOI: 10.1007/BF02658505
PC-1 content in skeletal muscle of non-obese, non-diabetic subjects: relationship to insulin receptor tyrosine kinase and whole body insulin sensitivity
Abstract
Insulin sensitivity varies widely in non-obese, non-diabetic subjects, and we have previously reported that in vivo insulin action correlates with in vitro insulin stimulated insulin receptor tyrosine-kinase activity in skeletal muscle. Plasma membrane glyco-protein PC-1 content is elevated in fibroblasts of insulin-resistant subjects, and expression of PC-1 cDNA in cultured cells reduces both insulin receptor tyrosine-kinase activity and the biological actions of insulin. In the present study we investigated non-obese, non-diabetic subjects and found a significant negative correlation between muscle PC-1 content and both in vivo insulin action as measured by the intravenous insulin tolerance test (r = -0.51, p = 0.035) and the sensitivity (ED50) of in vitro insulin stimulation of insulin receptor tyrosine-kinase activity (r = 0.66, p = 0.027). These studies indicate, therefore, that increased muscle PC-1 content is associated with reduced insulin action both in vivo and in vitro. Moreover, they suggest a possible role for PC-1 in regulating insulin receptor function in human skeletal muscle.
Similar articles
-
Decreased insulin receptor tyrosine kinase activity and plasma cell membrane glycoprotein-1 overexpression in skeletal muscle from obese women with gestational diabetes mellitus (GDM): evidence for increased serine/threonine phosphorylation in pregnancy and GDM.Diabetes. 2000 Apr;49(4):603-10. doi: 10.2337/diabetes.49.4.603. Diabetes. 2000. PMID: 10871198
-
Increased adipose tissue PC-1 protein content, but not tumour necrosis factor-alpha gene expression, is associated with a reduction of both whole body insulin sensitivity and insulin receptor tyrosine-kinase activity.Diabetologia. 1997 Mar;40(3):282-9. doi: 10.1007/s001250050675. Diabetologia. 1997. PMID: 9084965
-
Elevated plasma cell membrane glycoprotein levels and diminished insulin receptor autophosphorylation in obese, insulin-resistant rhesus monkeys.Metabolism. 2002 Apr;51(4):465-70. doi: 10.1053/meta.2002.31327. Metabolism. 2002. PMID: 11912555
-
Role of PC-1 in the etiology of insulin resistance.Ann N Y Acad Sci. 1999 Nov 18;892:204-22. doi: 10.1111/j.1749-6632.1999.tb07797.x. Ann N Y Acad Sci. 1999. PMID: 10842664 Review.
-
Membrane glycoprotein PC-1 and insulin resistance.Mol Cell Biochem. 1998 May;182(1-2):177-84. Mol Cell Biochem. 1998. PMID: 9609127 Review.
Cited by
-
Insulin signaling regulating genes: effect on T2DM and cardiovascular risk.Nat Rev Endocrinol. 2009 Dec;5(12):682-93. doi: 10.1038/nrendo.2009.215. Nat Rev Endocrinol. 2009. PMID: 19924153 Review.
-
Metabolic consequences of ENPP1 overexpression in adipose tissue.Am J Physiol Endocrinol Metab. 2011 Nov;301(5):E901-11. doi: 10.1152/ajpendo.00087.2011. Epub 2011 Aug 2. Am J Physiol Endocrinol Metab. 2011. PMID: 21810932 Free PMC article.
-
Association between the ENPP1 K121Q polymorphism and risk of diabetic kidney disease: a systematic review and meta-analysis.PLoS One. 2015 Mar 20;10(3):e0118416. doi: 10.1371/journal.pone.0118416. eCollection 2015. PLoS One. 2015. PMID: 25794151 Free PMC article.
-
Liver ENPP1 protein increases with remission of type 2 diabetes after gastric bypass surgery.BMC Gastroenterol. 2014 Dec 24;14:222. doi: 10.1186/s12876-014-0222-x. BMC Gastroenterol. 2014. PMID: 25539584 Free PMC article.
-
Studies of the relationship between the ENPP1 K121Q polymorphism and type 2 diabetes, insulin resistance and obesity in 7,333 Danish white subjects.Diabetologia. 2006 Sep;49(9):2097-104. doi: 10.1007/s00125-006-0353-x. Epub 2006 Jul 25. Diabetologia. 2006. PMID: 16865358
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials
Miscellaneous