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Palmitoleic Acid and Algae Extract Collaboration S. Vanessa Aguilar Dr. Christine Schmidt Dr. Rhykka Connelly 11/16/2011
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Yesterday we won intramural championship
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GOALS Algae Extract (fatty acid) Cancer 1 Diabetes 2 Others applications 1 Kato, et al, Nutrition and cancer, 2007. 2 Yang, et al, Lipids in health and disease, 2011.
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Background Using fatty acid-rich albumin in human embryonic stem cells (albuMAX) triggers adipogenic features. Ruiz-Vela et al., Stem Cell Rev and Rep 2011.
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Aims Optimization of biological activity of palmitoleic acid and algae extract using human dermal fibroblasts and an adequate vehicle Compare differences between palmitoleic acid and algae extract Develop a protocol to look at the internalization of lipids within cells
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Aim 1 Optimization of biological activity of palmitoleic acid and algae extract using human dermal fibroblasts and an adequate vehicle Develop a protocol to look at internalization of lipids within cells Compare differences between palmitoleic acid and algae extract
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Background Cell viability assay for fatty acid treatment – Vehicle Dimethylsulfoxide (DMSO) 1 Ethanol 2 – Concentration 10 μM 1 125 μM 1 1.Ruiz-Vela et al., Stem Cell Rev and Rep, 2011 2.Kato et al, Nutrition and Cancer, 2007
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Control max Ethanol vehicle 2.5 25 250 μM Control max DMSO vehicle 2.5 25 250 μM Methods Seed cells 5,000 cells/well Test palmitoleic acid concentration in ethanol and dimethylsulfoxide (DMSO). Check for proliferation using CellTiter 96 kit (Promega) 1, 2 and 3 days with tested media
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Palmitoleic Acid in DMSO DMSO itself is killing the cells 5% DMSO 250 μM can’t be tested using DMSO 2.5 μM and 25 μM of palmitoleic acid is safe
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2.5 PA μM in DMSO 3 Days 25 PA μM in DMSO 250 PA μM in DMSO Palmitoleic Acid in DMSO Control DMSO (highest 5%)
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Palmitoleic Acid in Ethanol 2.5 μM and 25 μM of palmitoleic acid is safe 250 μM of palmitoleic acid cells are not proliferating and dying
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3 Days 2.5 PA μM in Ethanol 25 PA μM in Ethanol 250 PA μM in Ethanol Control Ethanol (highest 5%) Palmitoleic acid in Ethanol
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Cell Morphology 250 PA μM in Ethanol 3 days 20x 250 PA μM in Ethanol 3 days 10x
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Controls Control Control DMSO (highest 5%) Control Ethanol (highest 5%) DMSO is killing cells.
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Cell Viability 2.5 uM and 25 uM of PA in both Ethanol and DMSO are safe to use with fibroblast in vitro
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Conclusions DMSO is not a good vehicle for palmitoleic acid. Ethanol is a good vehicle for lipids. There is a cell response with 250 μM palmitoleic acid.
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Aim 2 Find the range of palmitoleic acid and algae extract concentrations using human dermal fibroblast and the adequate vehicle Compare differences between palmitoleic acid and algae extract Develop a protocol to look at internalization of lipids within cells
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Test algae extract Algae extract was dried and weighed (58.7 mg) Dr. Connelly ran a gas solid chromatography to identify the lipid soluble components. – Results Fatty acids 2.864 mg – Myristic acid – 248 μg (8.6%) – Palmitic acid – 415.5 μg (14.5%) – Oleic acid – 85 μg (3%) – Palmitoleic acid – 1344 μg (47%) – Linoleic acid -200 μg (7%) – Linolenic acid- 96 μg (3.3% – Eicosapentaenoic acid -476 μg (16.6%) Other 55.83 mg – Carotenoids/xanthophills – Vitamins – Anything lipid soluble
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Methods Control 1 Control max Palmitoleic Acid 25 100 250 μM Control max Algae Extract 25 100 250 μM Control 2 Seed cells 2,500 cells/well Test palmitoleic acid concentration in ethanol and algae extract. Check for proliferation using CellTiter 96 kit (Promega) 1, 3 and 7 days with tested media. Ethanol vehicle
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Palmitoleic acid
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Algae Extract
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Cell Viability
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Conclusions Day 3 did not show increase of proliferation. – Checking on the images I took after adding MTS assay, my MTS assay was killing the cells. Day 7 there are no differences between controls, 25 μM, and 100 μM of Palmitoleic acid and 25 μM of algae extract.
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Aim 3 Find the range of palmitoleic acid and algae extract concentrations using human dermal fibroblast and the adequate vehicle Compare differences between palmitoleic acid and algae extract Develop a protocol to look at internalization of lipids within cells
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Methods After Cell titer 96 Fixed with 4% PFA at room temperature for 30°C minutes Rinse 3x5 in PBS Stained with LipidTox red Neutral stain (Invitrogen) 1:200 in PBS following Invitrogen protocol
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Controls Day 1 Control Cell Titer and Lipid Tox Control LipidTox only
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Palmitoleic Acid Day 1 Ethanol control 25 μM Palmitoleic acid 100 μM Palmitoleic acid 250 μM Palmitoleic acid
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Algae Extract Day 1 25 μM Algae extract100 μM Algae extract 250 μM Algae extract
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Palmitoleic acid day 3 Ethanol control 25 μM Palmitoleic acid 100 μM Palmitoleic acid 250 μM Palmitoleic acid
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25 uM Algae extract 100 uM Algae extract 250 uM Algae extract Algae Extract day 3
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Conclusions Qualitatively, there is an increase in lipids inside cells. Check pH of the testing media.
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