Oxidized HDL and Isoprostane Exert a Potent Adipogenic Effect on Stem Cells: Where in the Lineage?

The development of adipocytes in mice and humans follows a well-defined pathway that commences with a common pluripotent mesenchymal stem cell (MSC), ie., adipogenesis [1]. The early steps of the pathway leading to the generation and the commitment of MSCs to an adipocyte lineage are unknown. Hypothetically, the determination of the fate of MSCs occurs early in cell differentiation (“commitment”) and involves the interplay of intrinsic (genetic) and environmental (local and systemic) conditions that ultimately define the fate of the cell. Factors that determine MSC proliferation and differentiation also govern early adipocyte development and function. Currently, little is known about this process; from MSC-to-preadipocyte differentiation. However, the steps governing the transition from preadipocyte to adipocyte differentiation are not well defined (Figure 1). During adipogenesis MSCs or preadipocytes differentiate into lipid-laden adipocytes [2]. Ox-HDL increases adipogenic properties with a marked effect on the last step of adipocyte-terminal differentiation and release of adipokines including 20-HETE and Ang II.

[1]  R. Charnigo,et al.  Deficiency of Angiotensinogen in Hepatocytes Markedly Decreases Blood Pressure in Lean and Obese Male Mice , 2015, Hypertension.

[2]  M. Muñoz,et al.  Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis. , 2013, Clinical nephrology.

[3]  Xiaoli Shen,et al.  High-density lipoprotein nitration and chlorination catalyzed by myeloperoxidase impair its effect of promoting endothelial repair. , 2013, Free radical biology & medicine.

[4]  M. Barichella,et al.  Impaired fluidity and oxidizability of HDL hydrophobic core and amphipathic surface in dyslipidemic men. , 2013, Metabolism: clinical and experimental.

[5]  R. Saggini,et al.  Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low‐HDL Phenotype , 2013, Journal of the American Heart Association.

[6]  G. Favero,et al.  Heme induced oxidative stress attenuates sirtuin1 and enhances adipogenesis in mesenchymal stem cells and mouse pre‐adipocytes , 2012, Journal of cellular biochemistry.

[7]  R. Rezzani,et al.  High‐Fat Diet Exacerbates Renal Dysfunction in SHR: Reversal by Induction of HO‐1–Adiponectin Axis , 2012, Obesity.

[8]  L. Vítek The Role of Bilirubin in Diabetes, Metabolic Syndrome, and Cardiovascular Diseases , 2012, Front. Pharmacol..

[9]  R. Charnigo,et al.  Adipocyte-specific deficiency of angiotensinogen decreases plasma angiotensinogen concentration and systolic blood pressure in mice. , 2012, American journal of physiology. Regulatory, integrative and comparative physiology.

[10]  J. Falck,et al.  Crosstalk between EET and HO-1 downregulates Bach1 and adipogenic marker expression in mesenchymal stem cell derived adipocytes. , 2011, Prostaglandins & other lipid mediators.

[11]  L. Rodella,et al.  Adipocyte Heme Oxygenase-1 Induction Attenuates Metabolic Syndrome in Both Male and Female Obese Mice , 2010, Hypertension.

[12]  J. Gimble,et al.  Regulation of adipogenesis by natural and synthetic REV-ERB ligands. , 2010, Endocrinology.

[13]  N. Vaziri,et al.  HDL metabolism and activity in chronic kidney disease , 2010, Nature Reviews Nephrology.

[14]  J. Falck,et al.  Epoxyeicosatrienoic acid agonist regulates human mesenchymal stem cell-derived adipocytes through activation of HO-1-pAKT signaling and a decrease in PPARγ. , 2010, Stem cells and development.

[15]  S. Reddy,et al.  HDL as a Biomarker, Potential Therapeutic Target, and Therapy , 2009, Diabetes.

[16]  S. Reddy,et al.  Hemoglobin and Its Scavenger Protein Haptoglobin Associate with ApoA-1-containing Particles and Influence the Inflammatory Properties and Function of High Density Lipoprotein* , 2009, The Journal of Biological Chemistry.

[17]  M. Lazar,et al.  New developments in adipogenesis , 2009, Trends in Endocrinology & Metabolism.

[18]  I. Puddey,et al.  HDL is the major lipoprotein carrier of plasma F2-isoprostanes This work was supported by grants from the National Heart Foundation of Australia and the National Health and Medical Research Council of Australia. Published, JLR Papers in Press, December 2, 2008. , 2009, Journal of Lipid Research.

[19]  N. Torres,et al.  White adipose tissue as endocrine organ and its role in obesity. , 2008, Archives of medical research.

[20]  W. Aronow,et al.  Long-Term Treatment with the Apolipoprotein A1 Mimetic Peptide Increases Antioxidants and Vascular Repair in Type I Diabetic Rats , 2007, Journal of Pharmacology and Experimental Therapeutics.

[21]  G. Fonarow,et al.  The paradox of dysfunctional high-density lipoprotein , 2007, Current opinion in lipidology.

[22]  P. Montuschi,et al.  Insights into oxidative stress: the isoprostanes. , 2007, Current medicinal chemistry.

[23]  R. Korbut,et al.  Adipocytokines - novel link between inflammation and vascular function? , 2006, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[24]  H. Sumino,et al.  Angiotensin-II Receptor Antagonist Alleviates Non-alcoholic Fatty Liver in KKAy Obese Mice with Type 2 Diabetes , 2006, The Journal of international medical research.

[25]  S. Hazen,et al.  Formation of dysfunctional high-density lipoprotein by myeloperoxidase. , 2005, Trends in cardiovascular medicine.

[26]  P. Montuschi,et al.  Isoprostanes: markers and mediators of oxidative stress , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[27]  N. Abraham,et al.  Heme Oxygenase-1 Gene Expression Modulates Angiotensin II–Induced Increase in Blood Pressure , 2004, Hypertension.

[28]  N. Abraham,et al.  Expression of human heme oxygenase-1 in the thick ascending limb attenuates angiotensin II-mediated increase in oxidative injury. , 2004, Kidney international.

[29]  N. Abraham,et al.  Regulation of Cyclooxygenase- and Cytochrome P450-Derived Eicosanoids by Heme Oxygenase in the Rat Kidney , 2002, Hypertension.

[30]  D. Sugawara,et al.  Heme Oxygenase-1 Inhibits Atherogenesis in Watanabe Heritable Hyperlipidemic Rabbits , 2001, Circulation.

[31]  A. Lusis,et al.  Heme Oxygenase-1 Inhibits Atherosclerotic Lesion Formation in LDL-Receptor Knockout Mice , 2001, Circulation research.

[32]  A. Lusis,et al.  Induction of heme oxygenase-1 inhibits the monocyte transmigration induced by mildly oxidized LDL. , 1997, The Journal of clinical investigation.

[33]  E. Dickson,et al.  Endothelial cell hypoxia associated proteins are cell and stress specific , 1993, Journal of cellular physiology.

[34]  T. Sturgill,et al.  Angiotensinogen gene expression in 3T3-L1 cells. , 1989, The American journal of physiology.

[35]  I. London,et al.  On the origin of bile pigment in normal man. , 1950, The Journal of biological chemistry.

[36]  N. Abraham,et al.  Translational Significance of Heme Oxygenase in Obesity and Metabolic Syndrome. , 2016, Trends in pharmacological sciences.

[37]  G. Fonarow,et al.  Modifying the anti-inflammatory effects of high-density lipoprotein , 2007, Current atherosclerosis reports.