Nutrient deprivation increases vulnerability of endothelial cells to proinflammatory insults

Free Radical Biology and Medicine

Volumn 67, Issue , 2014, Pages 408-415

  Russell, Fraser D ^a   Hamilton, Karina D ^a  

^a UNIVERSITY OF THE SUNSHINE COAST   (Australia)

Author keywords

Free radicals; HUVECs; Reactive oxygen species; Serum deprivation; Superoxide; Tumor necrosis factor

Indexed keywords

MITOCHONDRIAL ENZYME; PHORBOL 13 ACETATE 12 MYRISTATE; SUPEROXIDE; TUMOR NECROSIS FACTOR ALPHA; CALCIUM CHANNEL; CULTURE MEDIUM; METHACRYLIC ACID DERIVATIVE; MITOCHONDRIAL CALCIUM UNIPORTER; MULTIENZYME COMPLEX; MYXOTHIAZOL; RUTHENIUM RED; THIAZOLE DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE 4;

ARTICLE; CELL ACTIVATION; CELL ADHESION; CONTROLLED STUDY; HUMAN; HUMAN CELL; NEUTROPHIL; NUTRIENT; PRIORITY JOURNAL; UMBILICAL VEIN ENDOTHELIAL CELL; ANTAGONISTS AND INHIBITORS; CHEMISTRY; COCULTURE; CULTURE MEDIUM; CYTOLOGY; DRUG EFFECTS; METABOLISM; OXIDATIVE STRESS; PHARMACOLOGY; CALCIUM TRANSPORT; CELL ISOLATION; CELL SUSPENSION; FOOD DEPRIVATION; NUTRIENT DEPRIVATION; PROTEIN EXPRESSION; RESPIRATORY CHAIN;

CALCIUM CHANNELS; CELL ADHESION; COCULTURE TECHNIQUES; CULTURE MEDIA, SERUM-FREE; ELECTRON TRANSPORT CHAIN COMPLEX PROTEINS; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; METHACRYLATES; NEUTROPHILS; OXIDATIVE STRESS; RUTHENIUM RED; SUPEROXIDES; TETRADECANOYLPHORBOL ACETATE; THIAZOLES; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84891709267     PISSN: 08915849     EISSN: 18734596     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2013.12.007     Document Type: Article

References (43)

1. H.K. Shin, Y.K. Kim, K.Y. Kim, J.H. Lee, and K.W. Hong Remnant lipoprotein particles induce apoptosis in endothelial cells by NAD(P)H oxidase-mediated production of superoxide and cytokines via lectin-like oxidized low-density lipoprotein receptor-1 activation: prevention by cilostazol Circulation 109 2004 1022 1028
2. O. Tricot, Z. Mallat, C. Heymes, J. Belmin, G. Lesèche, and A. Tedgui Relation between endothelial cell apoptosis and blood flow direction in human atherosclerotic plaques Circulation 101 2000 2450 2453
3. X.L. Du, G.Z. Sui, K. Stockklauser-Färber, J. Weiβ, S. Zink, B. Schwippert, Q.X. Wu, D. Tschöpe, and P. Rösen Induction of apoptosis by high proinsulin and glucose in cultured human umbilical vein endothelial cells is mediated by reactive oxygen species Diabetologia 41 1998 249 256
4. L. Quagliaro, L. Piconi, R. Assaloni, L. Martinelli, E. Motz, and A. Ceriello Intermittent high glucose enhances apoptosis related to oxidative stress in human umbilical vein endothelial cells: the role of protein kinase C and NAD(P)H-oxidase activation Diabetes 52 2003 2795 2804
5. T. Scarabelli, A. Stephanou, N. Rayment, E. Pasini, L. Comini, S. Curello, R. Ferrari, R. Knight, and D. Latchman Apoptosis of endothelial cells precedes myocyte cell apoptosis in ischemia/reperfusion injury Circulation 104 2001 253 256
6. S. Chrissobolis, A.A. Miller, G.R. Drummond, B.K. Kemp-Harper, and C.G. Sobey Oxidative stress and endothelial dysfunction in cerebrovascular disease Front. Biosci. 16 2011 1733 1745
7. H.A.R. Hadi, C.S. Carr, and J. Al Suwaidi Endothelial dysfunction: cardiovascular risk factors, therapy, and outcome Vasc. Health Risk Manage. 1 2005 183 198
8. S. Selemidis, C.G. Sobey, K. Wingler, H.H. Schmidt, and G.R. Drummond NADPH oxidases in the vasculature: molecular features, roles in disease and pharmacological inhibition Pharmacol. Ther. 120 2008 254 291
9. R.S. Frey, M. Ushio-Fukai, and A.B. Malik NADPH oxidase-dependent signaling in endothelial cells: role in physiology and pathophysiology Antioxid. Redox Signaling 11 2009 791 810
10. J.D. Lambeth, T. Kawahara, and B. Diebold Regulation of Nox and Duox enzymatic activity and expression Free Radic. Biol. Med. 43 2007 319 331
11. H.M. Peshavariya, G.J. Dusting, and S. Selemidis Analysis of dihydroethidium fluorescence for the detection of intracellular and extracellular superoxide produced by NADPH oxidase Free Radic. Res. 41 2007 699 712
12. S. Selemidis, G.J. Dusting, H. Peshavariya, B.K. Kemp-Harper, and G.R. Drummond Nitric oxide suppresses NADPH oxidase-dependent superoxide production by S-nitrosylation in human endothelial cells Cardiovasc. Res. 75 2007 349 358
13. cip1 and p53 Free Radic. Biol. Med. 43 2007 976 986
14. M. Nowicki, O. Zabirnyk, N. Duerrschmidt, J. Borlak, and K. Spanel-Borowski No upregulation of lectin-like oxidized low-density lipoprotein receptor-1 in serum-deprived EA.hy926 endothelial cells under oxLDL exposure, but increase in autophagy Eur. J. Cell Biol. 86 2007 605 616
15. S.R. Foster, E.R. Porrello, B. Purdue, H.-W. Chan, A. Voigt, S. Frenzel, R.D. Hannan, K.M. Moritz, D.G. Simmons, P. Molenaar, E. Roura, U. Boehm, W. Meyerhof, and W.G. Thomas Expression, regulation and putative nutrient-sensing function of taste GPCRs in the heart PLoS One 8 2013 e64579 2013
16. J. Wang, A. Alexanian, R. Ying, T.J. Kizhakekuttu, K. Dharmashankar, J. Vasquez-Vivar, D.D. Gutterman, and M.E. Widlansky Acute exposure to low glucose rapidly induces endothelial dysfunction and mitochondrial oxidative stress: role for AMP kinase Arterioscler. Thromb. Vasc. Biol. 32 2012 712 720
17. S. Karbach, T. Jansen, S. Horke, T. Heeren, A. Scholz, M. Coldewey, A. Karpi, M. Hausding, S. Kröller-Schön, M. Oelze, T. Münzel, and A. Daiber Hyperglycemia and oxidative stress in cultured endothelial cells - a comparison of primary endothelial cells with an immortalized endothelial cell line J. Diabetes Complications 26 2012 155 162
18. D. Vestweber Relevance of endothelial junctions in leukocyte extravasation and vascular permeability Ann. N. Y. Acad. Sci. 1257 2012 184 192
19. S.-J. Lin, S.-K. Shyue, Y.-Y. Hung, Y.-H. Chen, H.-H. Ku, J.-W. Chen, K.-B. Tam, and Y.-L. Chen Superoxide dismutase inhibits the expression of vascular cell adhesion molecule-1 and intracellular cell adhesion molecule-1 induced by tumor necrosis factor-α in human endothelial cells through the JNK/p38 pathways Arterioscler. Thromb. Vasc. Biol. 25 2005 334 340
20. B. Baudin, A. Bruneel, N. Bosselut, and M. Vaubourdolle A protocol for isolation and culture of human umbilical vein endothelial cells Nat. Protoc. 2 2007 481 485
21. L. Moldovan, N.I. Moldovan, R.H. Sohn, S.A. Parikh, and P.J. Goldschmidt-Clermont Redox changes of cultured endothelial cells and actin dynamics Circ. Res. 86 2000 549 557
22. O.H. Lowry, N.J. Rosebrough, A.L. Farr, and R.J. Randall Protein measurement with the Folin reagent J. Biol. Chem. 193 1951 265 275
23. R. Scherz-Shouval, E. Shvets, E. Fass, H. Shorer, L. Gil, and Z. Elazar Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4 EMBO J. 26 2007 1749 1760
24. I. Maestre, J. Jordán, S. Calvo, J.A. Reig, V. Ceña, B. Soria, M. Prentki, and E. Roche Mitochondrial dysfunction is involved in apoptosis induced by serum withdrawal and fatty acids in the β-cell line INS-1 Endocrinology 144 2003 335 345
25. S.B. Lee, J.J. Kim, T.W. Kim, B.S. Kim, M.-S. Lee, and Y.D. Yoo Serum deprivation-induced reactive oxygen species production is mediated by Romo1 Apoptosis 15 2010 204 218
26. P. Lijnen, V. Petrov, J. van Pelt, and R. Fagard Inhibition of superoxide dismutase induces collagen production in cardiac fibroblasts Am. J. Hypertens. 21 2008 1129 1136
27. S. Mankhetkorn, Z. Abedinzadeh, and C. Houee-Levin Antioxidant action of sodium diethyldithiocarbamate: reaction with hydrogen peroxide and superoxide radical Free Radic. Biol. Med. 17 1994 517 527
28. T.K.H. Chang, F.J. Gonzalez, and D.J. Waxman Evaluation of triacetyloleandomycin, α-nasymphthoflavone and diethyldithiocarbamate as selective chemical probes for inhibition of human cytochromes P450 Arch. Biochem. Biophys. 311 1994 437 442
29. S.O. Bachurin, E.P. Shevtzova, N.N. Lermontova, T.P. Serkova, and R.R. Ramsay The effect of dithiocarbamates on neurotoxic action of 1-methyl-4-phenyl-1,2,3,6 tetrahydropyridine (MPTP) and on mitochondrial respiration chain Neurotoxicology 17 1996 897 903
30. Y.S. Bae, H. Oh, S.G. Rhee, and Y.D. Yoo Regulation of reactive oxygen species generation in cell signalling Mol. Cells 32 2011 491 509
31. 2 production from mitochondrial respiratory chain Biochem. Biophys. Res. Commun. 281 2001 645 650
32. E.B. Tahara, F.D.T. Navarete, and A.J. Kowaltowski Tissue-, substrate-, and site-specific characteristics of mitochondrial reactive oxygen species generation Free Radic. Biol. Med. 46 2009 1283 1297
33. E. Jambrina, R. Alonso, M. Alcalde, M.C. Rodríguez, A. Serrano, C. Martínez-A, J. García-Sancho, and M. Izquierdo Calcium influx through receptor-operated channel induces mitochondria-triggered paraptotic cell death J. Biol. Chem. 278 2003 14134 14145
34. N.K. Isaev, E.V. Stelmashook, U. Dirnagl, E.Y. Plotnikov, E.A. Kuvshinova, and D.B. Zorov Mitochondrial free radical production induced by glucose deprivation in cerebellar granule neurons Biochemistry 73 2008 149 155
35. R. Moreno-Sánchez, L. Hernández-Esquivel, N.A. Rivero-Segura, A. Marín-Hernández, J. Neuzil, S.J. Ralph, and S. Rodríguez-Enríquez Reactive oxygen species are generated by the respiratory complex II - evidence for lack of contribution of the reverse electron flow in complex I FEBS J. 280 2013 927 938
36. W. Martinet, M.W.M. Knaapen, M.M. Kockx, and G.R.Y. De Meyer Autophagy in cardiovascular disease Trends Mol. Med. 13 2007 482 491
37. A. Lukasiewicz, J. Reszec, R. Kowalewski, L. Chyczewski, and U. Lebkowska Assessment of inflammatory infiltration and angiogenesis in the thrombus and the wall of abdominal aortic aneurysms on the basis of histological parameters and computed tomography angiography study Folia Histochem. Cytobiol. 50 2012 547 553
38. S. Cantara, S. Donnini, A. Giachetti, P.E. Thorpe, and M. Ziche Exogenous BH4/Bcl-2 peptide reverts coronary endothelial cell apoptosis induced by oxidative stress J. Vasc. Res. 41 2004 202 207
39. Y. Chen, M.B. Azad, and S.B. Gibson Superoxide is the major reactive oxygen species regulating autophagy Cell Death Differ. 16 2009 1040 1052
40. L. Li, Y. Chen, and S.B. Gibson Starvation-induced autophagy is regulated by mitochondrial reactive oxygen species leading to AMPK activation Cell Signalling 25 2013 50 65
41. J.L. Mehta, J. Chen, P.L. Hermonat, F. Romeo, and G. Novelli Lectin-like, oxidized low-density lipoprotein receptor-1 (LOX-1): a critical player in the development of atherosclerosis and related disorders Cardiovasc. Res. 69 2006 36 45
42. S. Jin, and E. White Role of autophagy in cancer: management of metabolic stress Autophagy 3 2007 28 31
43. G. Jia, G. Cheng, D.M. Gangahar, and D.K. Agrawal Insulin-like growth factor-1 and TNF-α regulate autophagy through c-jun N-terminal kinase and Akt pathways in human atherosclerotic vascular smooth cells Immunol. Cell Biol. 84 2006 448 454