DOI QR코드

DOI QR Code

Kr${\ddot}$ppel-Like Factor 2 Suppression by High Glucose as a Possible Mechanism of Diabetic Vasculopathy

  • Lee, Hae-Young (Cardiovascular Laboratory, Clinical Research Institute, Seoul National University Hospital) ;
  • Youn, Seock-Won (Cardiovascular Laboratory, Clinical Research Institute, Seoul National University Hospital) ;
  • Oh, Byung-Hee (Department of Internal Medicine, Seoul National University College of Medicine) ;
  • Kim, Hyo-Soo (Cardiovascular Laboratory, Clinical Research Institute, Seoul National University Hospital)
  • 발행 : 2012.04.30

초록

Background and Objectives: Endothelial dysfunction is widely observed in diabetes mellitus, resulting in diabetic vascular complications. Kr${\ddot}$ppel-like factor 2 (KLF2) is implicated as being a key molecule that maintains endothelial function. We evaluated the expression of KLF2 in endothelial cells cultured in high glucose and investigated its functional implication in a diabetic animal model. Subjects and Methods: Human umbilical vein endothelial cells (HUVECs) were cultured in physiologically high glucose (35 mM) condition. The Otsuka Long Evans Tokushima Fatty (OLETF) strain of rat was used as an excellent model of obese type II diabetes, and their lean littermates are Long Evans Tokushima Otsuka (LETO) rats. Results: In HUVECs cultured in physiologically high glucose condition, FOXO1 was activated whereas KLF2 and endothelial nitric oxide synthase (eNOS) expression was near completely abolished, which was completely reversed by FOXO1 small interfering ribonucleic acid. In the vessels harvested from the OLETF rats, the animal model of type II diabetes, KLF2 and eNOS expression were found depleted. When vascular remodeling was induced in the left common carotid artery by reduction of blood flow with partial ligation of the distal branches, greater neointimal hypertrophy was observed in OLETF rats compared with the control LETO rats. Conclusion: KLF2 suppression in endothelial cells by high glucose is a possible mechanism of diabetic endothelial dysfunction. The strategy of replenishing KLF2 may be effective for preventing diabetic vascular dysfunction.

키워드

참고문헌

  1. Haffner SM, Lehto S, Ronnemaa T, Pyorala K, Laakso M. Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction. N Engl J Med 1998;339:229-34. https://doi.org/10.1056/NEJM199807233390404
  2. Hink U, Li H, Mollnau H, et al. Mechanisms underlying endothelial dysfunction in diabetes mellitus. Circ Res 2001;88:E14-22. https://doi.org/10.1161/01.RES.88.2.e14
  3. De Vriese AS, Verbeuren TJ, Van de Voorde J, Lameire NH, Vanhoutte PM. Endothelial dysfunction in diabetes. Br J Pharmacol 2000;130:963-74. https://doi.org/10.1038/sj.bjp.0703393
  4. Johnstone MT, Creager SJ, Scales KM, Cusco JA, Lee BK, Creager MA. Impaired endothelium-dependent vasodilation in patients with insulin-dependent diabetes mellitus. Circulation 1993;88:2510-6. https://doi.org/10.1161/01.CIR.88.6.2510
  5. Balletshofer BM, Rittig K, Enderle MD, et al. Endothelial dysfunction is detectable in young normotensive first-degree relatives of subjects with type 2 diabetes in association with insulin resistance. Circulation 2000;101:1780-4. https://doi.org/10.1161/01.CIR.101.15.1780
  6. Hattori Y, Kawasaki H, Abe K, Kanno M. Superoxide dismutase recovers altered endothelium-dependent relaxation in diabetic rat aorta. Am J Physiol 1991;261(4 Pt 2):H1086-94.
  7. Beckman JA, Goldfine AB, Gordon MB, Garrett LA, Creager MA. Inhibition of protein kinase Cbeta prevents impaired endothelium-dependent vasodilation caused by hyperglycemia in humans. Circ Res 2002;90:107-11. https://doi.org/10.1161/hh0102.102359
  8. Steinberg HO, Chaker H, Leaming R, Johnson A, Brechtel G, Baron AD. Obesity/insulin resistance is associated with endothelial dysfunction: implications for the syndrome of insulin resistance. J Clin Invest 1996;97:2601-10. https://doi.org/10.1172/JCI118709
  9. Atkins GB, Jain MK. Role of Krüppel-like transcription factors in endothelial biology. Circ Res 2007;100:1686-95. https://doi.org/10.1161/01.RES.0000267856.00713.0a
  10. Samatar AA, Wang L, Mirza A, Koseoglu S, Liu S, Kumar CC. Transforming growth factor-beta 2 is a transcriptional target for Akt/protein kinase B via forkhead transcription factor. J Biol Chem 2002;277:28118-26. https://doi.org/10.1074/jbc.M203686200
  11. Buteau J, Accili D. Regulation of pancreatic beta-cell function by the forkhead protein FoxO1. Diabetes Obes Metab 2007;9(Suppl 2):140-6. https://doi.org/10.1111/j.1463-1326.2007.00782.x
  12. Kamagate A, Qu S, Perdomo G, et al. FoxO1 mediates insulin-dependent regulation of hepatic VLDL production in mice. J Clin Invest 2008;118:2347-64.
  13. Kim HS, Skurk C, Thomas SR, et al. Regulation of angiogenesis by glycogen synthase kinase-3beta. J Biol Chem 2002;277:41888-96. https://doi.org/10.1074/jbc.M206657200
  14. Kanemoto N, Hishigaki H, Miyakita A, et al. Genetic dissection of "OLETF", a rat model for non-insulin-dependent diabetes mellitus. Mamm Genome 1998;9:419-25. https://doi.org/10.1007/s003359900789
  15. Kumar A, Lindner V. Remodeling with neointima formation in the mouse carotid artery after cessation of blood flow. Arterioscler Thromb Vasc Biol 1997;17:2238-44. https://doi.org/10.1161/01.ATV.17.10.2238
  16. Korshunov VA, Berk BC. Flow-induced vascular remodeling in the mouse: a model for carotid intima-media thickening. Arterioscler Thromb Vasc Biol 2003;23:2185-91. https://doi.org/10.1161/01.ATV.0000103120.06092.14
  17. Wang N, Miao H, Li YS, et al. Shear stress regulation of Kruppel-like factor 2 expression is flow pattern-specific. Biochem Biophys Res Commun 2006;341:1244-51. https://doi.org/10.1016/j.bbrc.2006.01.089
  18. Parmar KM, Larman HB, Dai G, et al. Integration of flow-dependent endothelial phenotypes by Kruppel-like factor 2. J Clin Invest 2006;116:49-58.
  19. Hurks R, Eisinger MJ, Goovaerts I, et al. Early endothelial dysfunction in young type 1 diabetics. Eur J Vasc Endovasc Surg 2009;37:611-5. https://doi.org/10.1016/j.ejvs.2009.01.015
  20. Baris N, Akdeniz B, Uyar S, et al. Are complex coronary lesions more frequent in patients with diabetes mellitus? Can J Cardiol 2006;22:935-7. https://doi.org/10.1016/S0828-282X(06)70312-9
  21. Iakovou I, Schmidt T, Bonizzoni E, et al. Incidence, predictors, and outcome of thrombosis after successful implantation of drug-eluting stents. JAMA 2005;293:2126-30. https://doi.org/10.1001/jama.293.17.2126
  22. Parmar KM, Nambudiri V, Dai G, Larman HB, Gimbrone MA Jr, Garcia-Cardena G. Statins exert endothelial atheroprotective effects via the KLF2 transcription factor. J Biol Chem 2005;280:26714-9. https://doi.org/10.1074/jbc.C500144200
  23. Rossi J, Rouleau L, Tardif JC, Leask RL. Effect of simvastatin on Kruppel-like factor2, endothelial nitric oxide synthase and thrombomodulin expression in endothelial cells under shear stress. Life Sci 2010;87:92-9. https://doi.org/10.1016/j.lfs.2010.05.008
  24. Arslan F, Pasterkamp G, de Kleijn DP. Unraveling pleiotropic effects of statins: bit by bit, a slow case with perspective. Circ Res 2008;103:334-6. https://doi.org/10.1161/CIRCRESAHA.108.182220
  25. Thum T, Bauersachs J. Sports or statins for atheroprotection? New insight from Kruppel-like factor 2. Cardiovasc Res 2006;72:193-5. https://doi.org/10.1016/j.cardiores.2006.08.016

피인용 문헌

  1. FOXO1 impairs whereas statin protects endothelial function in diabetes through reciprocal regulation of Kruppel-like factor 2. vol.97, pp.1, 2012, https://doi.org/10.1093/cvr/cvs283
  2. Catechin Averts Experimental Diabetes Mellitus-Induced Vascular Endothelial Structural and Functional Abnormalities vol.14, pp.1, 2012, https://doi.org/10.1007/s12012-013-9226-y
  3. Blood pressure regulation VIII: resistance vessel tone and implications for a pro-atherogenic conduit artery endothelial cell phenotype vol.114, pp.3, 2014, https://doi.org/10.1007/s00421-013-2684-x
  4. Vascular Adaptation to Exercise in Humans: Role of Hemodynamic Stimuli vol.97, pp.2, 2017, https://doi.org/10.1152/physrev.00014.2016
  5. COMP-Angiopoietin-1 accelerates muscle regeneration through N-cadherin activation vol.8, pp.None, 2012, https://doi.org/10.1038/s41598-018-30513-7
  6. A20/TNFAIP3 Increases ENOS Expression in an ERK5/KLF2-Dependent Manner to Support Endothelial Cell Health in the Face of Inflammation vol.8, pp.None, 2012, https://doi.org/10.3389/fcvm.2021.651230
  7. The Role of Epidermal Growth Factor Receptor Family of Receptor Tyrosine Kinases in Mediating Diabetes-Induced Cardiovascular Complications vol.12, pp.None, 2021, https://doi.org/10.3389/fphar.2021.701390