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Glutamine utilization by rat neutrophils: presence of phosphate-dependent glutaminase
T. C. Curi, M. P. De Melo, R. B. De Azevedo, T. M. Zorn and R. Curi Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of Sao Paulo, SP, Brazil. The capacity of rat neutrophils to utilize glutamine was investigated by 1) determination of oxygen consumption in the p...
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Published in: | American Journal of Physiology: Cell Physiology 1997-10, Vol.273 (4), p.C1124-C1129 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
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Online Access: | Get full text |
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Summary: | T. C. Curi, M. P. De Melo, R. B. De Azevedo, T. M. Zorn and R. Curi
Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of Sao Paulo, SP, Brazil.
The capacity of rat neutrophils to utilize glutamine was investigated by 1)
determination of oxygen consumption in the presence of glucose or
glutamine, 2) measurement of maximal activity of phosphate-dependent
glutaminase, 3) Northern blot, Western blot, and immunocytochemical
detection of glutaminase, and 4) measurement of glutamine utilization and
also production of ammonia, glutamate, aspartate, alanine, and lactate and
decarboxylation of [U-14C]glutamine in cells incubated for 1 h. The rate of
respiration by isolated neutrophils in the absence of added substrate was
5.0 nmol x min(-1) x 10(7) cells(-1). Maximal activity of
phosphate-dependent glutaminase was 56 nmol x min(-1) x mg protein(-1) in
freshly obtained neutrophils; the Michaelis-Menten constant was 3.5 mM for
glutamine. This enzyme activity was inhibited by 2 mM glutamate, 2 mM
oxoglutarate, and 2 mM NH4Cl. The presence of glutaminase protein (65 kDa)
was confirmed by Western blot and immunocytochemical detection and the
presence of the mRNA (6.0 kb) by Northern blot analysis. Glutamine was
utilized by neutrophils incubated for 1 h at a rate of 12.8 nmol x min(-1)
x mg protein(-1) when the amino acid was added to the medium at 2 mM, which
is three to four times higher than the physiological concentration. In the
presence of 0.5 mM glutamine, the amino acid was utilized at a rate of 2.9
nmol x min(-1) x mg protein(-1). The addition of 0.5 mM glutamate to the
incubation medium caused a marked reduction (by 70%) in glutamine
utilization by neutrophils. Glucose was utilized at 7.7 nmol x min(-1) x mg
protein(-1) when cells were incubated in 5 mM glucose. The conversion of
[U-14C]glutamine to 14CO2 was very low: |
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ISSN: | 0363-6143 1522-1563 |
DOI: | 10.1152/ajpcell.1997.273.4.c1124 |