Oxygen metabolism in human placenta mitochondria

Journal of Bioenergetics and Biomembranes

Volumn 46, Issue 6, 2014, Pages 459-469

  Bustamante, J ^a   Ramirez Velez R ^b   Czerniczyniec, A ^a   Cicerchia, D ^a   Aguilar de Plata, A C ^b   Lores Arnaiz, S ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^b UNIVERSIDAD DEL VALLE   (Colombia)

Author keywords

Apoptosis; Cardiolipin; Free radicals; Human placenta mitochondria; Hydrogen peroxide

Indexed keywords

CARDIOLIPIN; CYTOCHROME C; CYTOCHROME P450; HYDROGEN PEROXIDE; LACTATE DEHYDROGENASE; OXYGEN; PROTEIN BAX; PROTEIN P53; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; FREE RADICAL;

ARTICLE; CELL ORGANELLE; CHEMOLUMINESCENCE; CYTOTROPHOBLAST; ENZYME ACTIVITY; FLOW CYTOMETRY; HUMAN; MITOCHONDRIAL MEMBRANE POTENTIAL; MITOCHONDRION; OXYGEN CONSUMPTION; PLACENTA; PROTON MOTIVE FORCE; RESPIRATION CONTROL; RESPIRATORY CHAIN; RESPIRATORY FUNCTION; SYNCYTIOTROPHOBLAST; WESTERN BLOTTING; ADULT; APOPTOSIS; FEMALE; METABOLISM; PHYSIOLOGY; PREGNANCY; YOUNG ADULT;

ADULT; APOPTOSIS; FEMALE; FREE RADICALS; HUMANS; HYDROGEN PEROXIDE; MITOCHONDRIA; OXYGEN; PLACENTA; PREGNANCY; YOUNG ADULT;

EID: 84916593968     PISSN: 0145479X     EISSN: 15736881     Source Type: Journal    
DOI: 10.1007/s10863-014-9572-x     Document Type: Article

References (39)

1. Boveris A, Valdez LB, Zaobornyj T, Bustamante J (2006) Mitochondrial metabolic states regulate nitric oxide and hydrogen peroxide diffusion to the cytosol. Biochim Biophys Acta 1757:535–542
2. Bustamante J, Lores-Arnaiz S (2010) Characteristics of the permeability transition in brain cortex mitochondria. In: Svensson OL (ed) Mitochondria, structure, functions and dysfunctions. Nova Biomedical Books, New York, pp 829–847
3. Bustamante J, Di Libero E, Monti N, Fernandez-Cobo M, Cadenas E, Boveris A (2004) Kinetic analysis of thapsigargin-induced thymocyte apoptosis. Free Radic Biol Med 37:1490–1498
4. Bustamante J, Lores-Arnaiz S, Tallis S, Roselló DM, Lago N, Lemberg A, Boveris A, Perazzo JC (2011) Mitochondrial dysfunction as a mediator of hippocampal apoptosis in a model of hepatic encephalopathy. Mol Cell Biochem 354:23–40
5. Carlin A, Alfirevic Z (2008) Physiological changes of pregnancy and monitoring. Best Pract Res Clin Obstet Gynaecol 22:801–823
6. Chance B, Williams GR (1956) The respiratory chain and oxidative phosphorylation. Adv Enzymol Relat Areas Mol Biol 17:65–134
7. Chipuk JE, Bouchier-Hayes L, Green DR (2006) Mitochondrial outer membrane permeabilization during apoptosis: the innocent bystander scenario. Cell Death Differ 13:1396–1402
8. Colleoni F, Lattuada D, Garretto A, Massari M, Mandò C, Somigliana E, Cetin I (2010) Maternal blood mitochondrial DNA content during normal and intrauterine growth restricted (IUGR) pregnancy. Am J Obstet Gynecol 203:1–6
9. Cossarizza A, Ceccarelli D, Masini A (1996) Functional heterogenity of an isolated mitochondrial population revealed by cytofluorometric analysis at the single organelle level. Exp Cell Res 222(1):84–94
10. Crivello JF, Hornsby PJ, Gill GN (1983) Suppression of cultured bovine adrenocortical zone glomerulus cell aldosterone synthesis by steroids and its prevention by antioxidants. Endocrinology 113:235–242
11. Crocker IP, Barratt S, Kaur M, Baker P (2001) The in-vitro characterization of induced apoptosis in placental cytotrophoblasts and syncytiotrophoblasts. Placenta 22:822–830
12. Estabrook RW (1967) Mitochondrial respiratory control and the polarographic measurement of ADP: o ratios. Methods Enzymol 10:41–47
13. Gellerich FN, Ulrich J, Kunz W (1994) Unusual properties of mitochondria from the human term placenta are caused by alkaline phosphatase. Placenta 15:299–310
14. Hanukoglu I (2006) Antioxidant protective mechanisms against reactive oxygen species (ROS) generated by mitochondrial P450 systems in steroidogenic cells. Drug Metab Rev 38(1–2):171–96
15. Heazell AEP, Crocker IP (2008) Live and let die- regulation of villous trophoblast apoptosis in normal and abnormal pregnancies. Placenta 29:772–783
16. Jacobson J, Duchen MR, Heales SJ (2002) Intracellular distribution of the fluorescent dye nonyl acridine orange responds to the mitochondrial membrane potential: implications for assays of cardiolipin and mitochondrial mass. J Neurochem 82(2):224–233
17. Karadayian AG, Bustamante J, Czerniczyniec A, Cutrera RA, Lores-Arnaiz S (2014) Effect of melatonin on motor performance and brain cortex mitochondrial function during ethanol hangover. Neuroscience 269:281–289
18. Klimek J (1988) The involvement of superoxide and iron ions in the NADPH-dependent lipid peroxidation in human placental mitochondria. Biochim Biophys Acta 958:31–39
19. Klimek J (1990) Cytochrome P-450 involvement in the NADPH-dependent lipid peroxidation in human placental mitochondria. Biochim Biophys Acta 1044:158–164
20. Klimek J, Woźniak M, Szymańska G, Zelewski L (1998) Inhibitory effect of free radicals derived from organic hydroperoxide on progesterone synthesis in human term placental mitochondria. Free Radic Biol Med 24:1168–1175
21. Longtine MS, Barton A, Chen B, Nelson DM (2012a) Live-cell imaging shows apoptosis initiates locally and propagates as a wave throughout syncytiotrophoblasts in primary cultures of human placental villous trophoblasts. Placenta 33:971–976
22. Longtine MS, Chen B, Odibo AO, Zhong Y, Nelson DM (2012b) Villous trophoblast apoptosis is elevated and restricted to cytotrophoblasts in pregnancies complicated by preeclampsia, IUGR, or preeclampsia with IUGR. Placenta 33:352–359
23. Longtine MS, Chen B, Odibo AO, Zhong Y, Nelson DM (2012c) Caspase-mediated apoptosis of trophoblasts in term human placental villi is restricted to cytotrophoblasts and absent from the multinucleated syncytiotrophoblast. Reproduction 143(1):107–121
24. Lowry OH, Rosenbrough NH, Farr AL, Randall JR (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275
25. Mandò C, De Palma C, Stampalija T, Anelli GM, Figus M, Novielli C, Parisi F, Clementi E, Ferrazzi E, Cetin I (2014) Placental mitochondrial content and function in intrauterine growth restriction and preeclampsia. Am J Physiol Endocrinol Metab 306(4):E404–413
26. Martínez F, Espinosa-García T, Flores-Herrera O, Pardo JP (1993) Respiratory control induced by ATP in human term placental mitochondria. Placenta 14:321–331
27. Martínez F, Meaney A, Espinosa-García MT, Pardo JP, Uribe A, Flores-Herrera O (1996) Characterization of the F1F0-ATPase and the tightly-bound ATPase activities in submitochondrial particles from human term placenta. Placenta 17:345–350
28. Martínez F, Kiriakidou M, Strauss JF (1997) III Structural and functional changes in mitochondria associated with trophoblast differentiation: methods to isolate enriched preparations of syncytiotrophoblast mitochondria. Endocrinology 138:2172–2183
29. Mattiasson G, Friberg H, Hansson M, Elmér E, Wieloch T (2003) Flow cytometric analysis of mitochondria from CA1 and CA3 regions of rat hippocampus reveals differences in permeability transition pore activation. J Neurochem 87:532–544
30. Matttiasson G (2004) Flow cytometry analysis of isolated liver mitochondria, to detect changes relevant to cell death. Cytometry A 60(2):145–154
31. 450 and steroid biosynthesis in the human placenta. Biochim Biophys Acta 165:476–482
32. Meigs RA, Sheean LA (1977) Mitochondria from human term placenta. III. The role of respiration and energy generation in progesterone biosynthesis. Biochim Biophys Acta 489:225–235
33. Omura T, Sato R (1964) The carbon monoxide-binding pigment of liver microsomes. II. solubilization, purification, and properties. J Biol Chem 239:2379–2385
34. Petrosillo G, Ruggiero FM, Paradies G (2003) Role of reactive oxygen species and cardiolipin in the release of cytochrome c from mitochondria. FASEB J 17:2202–2208
35. Petrosillo G, Portincasa P, Grattagliano I, Casanova G, Matera M, Ruggiero FM, Ferri D, Paradies G (2007) Mitochondrial dysfunction in rat with nonalcoholic fatty liver involvement of complex I, reactive oxygen species and cardiolipin. Biochim Biophys Acta 1767:1260–1267
36. Ramírez-Vélez R, Bustamante J, Czerniczyniec A, Aguilar de Plata AC, Lores-Arnaiz S (2013) Effect of exercise training on Enos expression, NO production and oxygen metabolism in human placenta. PLoS One 8(11):e80225. doi:10.1371/journal.pone.0080225
37. Straszewski-Chavez SL, Abrahams VM, Mor G (2005) The role of apoptosis in the regulation of trophoblast survival and differentiation during pregnancy. Endocr Rev 26:877–897
38. Vousden KH, Lane DP (2007) P53 in health and disease. Nat Rev Mol Cell Biol 8:275–283
39. Wooding FB, Flint AP (1994) Marshall’s physiology of reproduction, 4th edn. Chapman & Hall, London