Glucose metabolism in cultured trophoblasts from human placenta
Conference
·
· FASEB Journal (Federation of American Societies for Experimental Biology); (United States)
OSTI ID:6010847
- Washington Univ., St. Louis, MO (United States)
The development of appropriate placental trophoblast isolation and culture techniques enables the study of pathways of glucose utilization by this important cell layer in vitro. Trophoblasts from normal term placentas were isolated and cultured 24 hours and 72 hours in uncoated polystyrene culture tubes or tubes previously coated with a fibrin matrix. Trophoblasts cultured on fibrin are morphologically distinct from those cultured on plastic or other matrices and generally resemble in vivo syncytium. Cells were incubated up to 3 hours with {sup 14}C-labeled glucose and reactions were stopped by addition of perchloric acid. {sup 14}CO{sub 2} production by trophoblasts increased linearly with time however the largest accumulation of label was in organic acids. Trophoblasts cultured in absence of fibrin utilized more glucose and accumulated more {sup 14}C in metabolic products compared to cells cultured on fibrin. Glucose oxidation to CO{sub 2} by the phosphogluconate (PG) pathway was estimated from specific yields of {sup 14}CO{sub 2} from (1-{sup 14}C)-D-glucose and (6-{sup 14}C)-D-glucose. Approximately 6% of glucose oxidation was by the PG pathway when cells were cultured on fibrin compared to approximately 1% by cells cultured in the absence of fibrin. The presence of a fibrin growth matrix appears to modulate the metabolism of glucose by trophoblast from human placenta in vitro.
- OSTI ID:
- 6010847
- Report Number(s):
- CONF-9104107--
- Conference Information:
- Journal Name: FASEB Journal (Federation of American Societies for Experimental Biology); (United States) Journal Volume: 4:3
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550501* -- Metabolism-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDES
ANIMAL CELLS
BIOLOGICAL PATHWAYS
BLOOD COAGULATION FACTORS
CARBOHYDRATES
CARBON 14 COMPOUNDS
CARBON COMPOUNDS
CARBON DIOXIDE
CARBON OXIDES
CELL CULTURES
CHALCOGENIDES
COAGULANTS
CULTURE MEDIA
DRUGS
EMBRYONIC CELLS
FETAL MEMBRANES
FIBRIN
GLUCOSE
HEMATOLOGIC AGENTS
HEMOSTATICS
HEXOSES
IN VITRO
ISOTOPE APPLICATIONS
LABELLED COMPOUNDS
MEMBRANES
METABOLISM
MONOSACCHARIDES
ORGANIC COMPOUNDS
OXIDES
OXYGEN COMPOUNDS
PLACENTA
PROTEINS
SACCHARIDES
SCLEROPROTEINS
TRACER TECHNIQUES
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDES
ANIMAL CELLS
BIOLOGICAL PATHWAYS
BLOOD COAGULATION FACTORS
CARBOHYDRATES
CARBON 14 COMPOUNDS
CARBON COMPOUNDS
CARBON DIOXIDE
CARBON OXIDES
CELL CULTURES
CHALCOGENIDES
COAGULANTS
CULTURE MEDIA
DRUGS
EMBRYONIC CELLS
FETAL MEMBRANES
FIBRIN
GLUCOSE
HEMATOLOGIC AGENTS
HEMOSTATICS
HEXOSES
IN VITRO
ISOTOPE APPLICATIONS
LABELLED COMPOUNDS
MEMBRANES
METABOLISM
MONOSACCHARIDES
ORGANIC COMPOUNDS
OXIDES
OXYGEN COMPOUNDS
PLACENTA
PROTEINS
SACCHARIDES
SCLEROPROTEINS
TRACER TECHNIQUES