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Bioenergetics and mitochondrial transmembrane potential during differentiation of cultured osteoblasts
1 Life Sciences Division, NASA Ames Research Center, Moffett Field, California 94035-1000; and 2 National Research Center for Hematology, Moscow, 125167 Russia To evaluate the relationship between osteoblast differentiation and bioenergetics, cultured primary osteoblasts from fetal rat calvaria we...
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Published in: | American Journal of Physiology: Cell Physiology 2000-10, Vol.279 (4), p.C1220-C1229 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 1 Life Sciences Division, NASA Ames Research Center, Moffett
Field, California 94035-1000; and 2 National Research Center
for Hematology, Moscow, 125167 Russia
To evaluate the
relationship between osteoblast differentiation and bioenergetics,
cultured primary osteoblasts from fetal rat calvaria were grown in
medium supplemented with ascorbate to induce differentiation. Before
ascorbate treatment, the rate of glucose consumption was 320 nmol · h 1 · 10 6
cells 1 , respiration was 40 nmol · h 1 · 10 6
cells 1 , and the ratio of lactate production to glucose
consumption was ~2, indicating that glycolysis was the main energy
source for immature osteoblasts. Ascorbate treatment for 14 days led to
a fourfold increase in respiration, a threefold increase in ATP production, and a fivefold increase in ATP content compared with that
shown in immature cells. Confocal imaging of mitochondria stained with
a transmembrane potential-sensitive vital dye showed that mature cells
possessed abundant amounts of high-transmembrane-potential mitochondria, which were concentrated near the culture medium-facing surface. Acute treatment of mature osteoblasts with metabolic inhibitors showed that the rate of glycolysis rose to maintain the
cellular energy supply constant. Thus progressive differentiation coincided with changes in cellular metabolism and mitochondrial activity, which are likely to play key roles in osteoblast function.
ATP; respiration; glycolysis; bone |
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ISSN: | 0363-6143 1522-1563 |
DOI: | 10.1152/ajpcell.2000.279.4.c1220 |