Namgaladze 2010 Atherosclerosis: Difference between revisions
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|abstract=Low density lipoprotein modified by secretory phospholipase A2 (PLA-LDL) protects monocytes againstΒ΄oxidative stress. In this study we investigated possible direct effects of PLA-LDL on mitochondrial membrane potential and reactive oxygen species generation. Mitochondrial membrane potential in human monocytic THP-1 cells or primary human monocytes was monitored by flow cytometry using the fluorescent dye 5,5',6,6'-tetrachloro-1,1',3,3'- tetraethylbenzimidazolylcarbocyanine iodide or respirometry. Formation of reactive oxygen species was determined by flow cytometric measuring 2',7'-dichlorofluorescin oxidation. Cell death was assessed using Annexin V/propidium iodide staining. We observed that PLA-LDL caused mitochondrial uncoupling in monocyte/macrophage cell lines as well as in primary human monocytes. PLA-LDL-associated non-esterified fatty acids provoked uncoupling. Uncoupling attenuated reactive oxygen species formation induced by hydrogen peroxide, 2,3-dimethoxy-1,4-naphthoquinone or oxidized LDL. Knock-down of uncoupling protein UCP2 affected neither PLA-LDL-induced uncoupling, nor reactive oxygen species generation. Furthermore,we observed that the chemical uncoupler carbonyl cyanide m-chlorophenylhydrazone increased THP-1 cell survival after hydrogen peroxide treatment. Thus, PLA-LDL-induced uncoupling attenuates reactive oxygen species generation, which may contribute to increased monocyte survival in atherosclerotic plaques and support pro-atherogenic effects of LDL modified by PLA2. | |abstract=Low density lipoprotein modified by secretory phospholipase A2 (PLA-LDL) protects monocytes againstΒ΄oxidative stress. In this study we investigated possible direct effects of PLA-LDL on mitochondrial membrane potential and reactive oxygen species generation. Mitochondrial membrane potential in human monocytic THP-1 cells or primary human monocytes was monitored by flow cytometry using the fluorescent dye 5,5',6,6'-tetrachloro-1,1',3,3'- tetraethylbenzimidazolylcarbocyanine iodide or respirometry. Formation of reactive oxygen species was determined by flow cytometric measuring 2',7'-dichlorofluorescin oxidation. Cell death was assessed using Annexin V/propidium iodide staining. We observed that PLA-LDL caused mitochondrial uncoupling in monocyte/macrophage cell lines as well as in primary human monocytes. PLA-LDL-associated non-esterified fatty acids provoked uncoupling. Uncoupling attenuated reactive oxygen species formation induced by hydrogen peroxide, 2,3-dimethoxy-1,4-naphthoquinone or oxidized LDL. Knock-down of uncoupling protein UCP2 affected neither PLA-LDL-induced uncoupling, nor reactive oxygen species generation. Furthermore,we observed that the chemical uncoupler carbonyl cyanide m-chlorophenylhydrazone increased THP-1 cell survival after hydrogen peroxide treatment. Thus, PLA-LDL-induced uncoupling attenuates reactive oxygen species generation, which may contribute to increased monocyte survival in atherosclerotic plaques and support pro-atherogenic effects of LDL modified by PLA2. | ||
|keywords=Atherosclerosis, Phagocytes, Reactive oxygen species, Phospholipase A2, LDL, Human monocytic THP-1 cells, Primary human monocytes, | |keywords=Atherosclerosis, Phagocytes, Reactive oxygen species, Phospholipase A2, LDL, Human monocytic THP-1 cells, Primary human monocytes, | ||
|mipnetlab= | |mipnetlab=DE Frankfurt Brandt U, DE Frankfurt Droese S | ||
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Revision as of 16:53, 17 March 2015
Namgaladze D, Preiss S, DrΓΆse S, Brandt U, BrΓΌne B (2010) Phospholipase A2-modified low density lipoprotein induces mitochondrial uncoupling and lowers reactive oxygen species in phagocytes. Atherosclerosis 208:142-7. |
Namgaladze D, Preiss S, Droese S, Brandt U, Bruene B (2010) Atherosclerosis
Abstract: Low density lipoprotein modified by secretory phospholipase A2 (PLA-LDL) protects monocytes againstΒ΄oxidative stress. In this study we investigated possible direct effects of PLA-LDL on mitochondrial membrane potential and reactive oxygen species generation. Mitochondrial membrane potential in human monocytic THP-1 cells or primary human monocytes was monitored by flow cytometry using the fluorescent dye 5,5',6,6'-tetrachloro-1,1',3,3'- tetraethylbenzimidazolylcarbocyanine iodide or respirometry. Formation of reactive oxygen species was determined by flow cytometric measuring 2',7'-dichlorofluorescin oxidation. Cell death was assessed using Annexin V/propidium iodide staining. We observed that PLA-LDL caused mitochondrial uncoupling in monocyte/macrophage cell lines as well as in primary human monocytes. PLA-LDL-associated non-esterified fatty acids provoked uncoupling. Uncoupling attenuated reactive oxygen species formation induced by hydrogen peroxide, 2,3-dimethoxy-1,4-naphthoquinone or oxidized LDL. Knock-down of uncoupling protein UCP2 affected neither PLA-LDL-induced uncoupling, nor reactive oxygen species generation. Furthermore,we observed that the chemical uncoupler carbonyl cyanide m-chlorophenylhydrazone increased THP-1 cell survival after hydrogen peroxide treatment. Thus, PLA-LDL-induced uncoupling attenuates reactive oxygen species generation, which may contribute to increased monocyte survival in atherosclerotic plaques and support pro-atherogenic effects of LDL modified by PLA2. β’ Keywords: Atherosclerosis, Phagocytes, Reactive oxygen species, Phospholipase A2, LDL, Human monocytic THP-1 cells, Primary human monocytes
β’ O2k-Network Lab: DE Frankfurt Brandt U, DE Frankfurt Droese S
Labels:
Pathology: Cancer
Stress:Oxidative stress;RONS
Organism: Human
Tissue;cell: Blood cells
Preparation: Intact cells
Enzyme: Uncoupling protein
HRR: Oxygraph-2k