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Ammonia production by IMR‐90 fibroblast cultures: Effects of ammonia on glutathione, γ‐glutamyl transpeptidase, lysosomal enzymes, and cell division

Identifieur interne : 003544 ( Main/Exploration ); précédent : 003543; suivant : 003545

Ammonia production by IMR‐90 fibroblast cultures: Effects of ammonia on glutathione, γ‐glutamyl transpeptidase, lysosomal enzymes, and cell division

Auteurs : Shizuko Takahashi [États-Unis] ; Sachiko Nakagawa [États-Unis] ; Maria Zeydel [États-Unis] ; Girija Bhargava [États-Unis]

Source :

RBID : ISTEX:980B1E1A7F979E7C1A78F17092FDAEE2A7E34910

English descriptors

Abstract

γ‐Glutamyl transpeptidase has multi‐catalytic activities. It degrades glutathi‐one and can produce ammmonia from glutamine. The present study was designed to examine whether the decreased cell proliferation, cellular gluta‐thione content and concurrent increase in ammonia production in senescent cells in culture are the result of increased γ‐glutamyl transpeptidase activity. We used IMR‐90 fibroblast and 3T3 LI preadipocyte cultures. The cellular glutathione content depended upon cell proliferation and cell density. The glutathione content was higher in cells at logarithmic growth, and lower at stationary growth or post confluency; dead cells had no detectable glutathione by the method currently used. The glutathione content was minimal in “old” IMR‐90 cells, regardless of cell density. On the other hand, an increase occurred in the unit number of molecules of bound 5‐iodoacetoamidofluorescein, an active‐site directed stoichiometric inhibitor of transpeptidase. That result corresponded favorably with the increased enzyme activity, suggesting that the number of enzyme molecules per cell was increased. The inhibition of ammonia production of the cultures by inhibition of γ‐glutamyl transpeptidase by 5‐iodoacetoamidofluorescein and reversible inhibition of ammonia production by a serine‐borate mixture were consistent with our postulate. Addition of NH4Cl (0.1 mM) to IMR‐90 cultures caused increased activities of transpeptidase and some of the lysosomal enzymes; concurrently, the amount of cellular glutathione and the number of cell divisions decreased. This suggests that the increased ammonia production presumably resulting from glutaminase activity of the observed increase of transpeptidase may profoundly affect certain cellular functions.

Url:
DOI: 10.1002/jcp.1041250114


Affiliations:


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Le document en format XML

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<term>Biophys</term>
<term>Cell density</term>
<term>Cell proliferation</term>
<term>Cell viability</term>
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<term>Cellular glutathione</term>
<term>Cellular glutathione content</term>
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<term>Enzyme activities</term>
<term>Enzyme activity</term>
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<term>Ggtp activity</term>
<term>Glutaminase activity</term>
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<term>Glutathione content</term>
<term>Higher glutathione content</term>
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<term>Logarithmic growth</term>
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<term>Lysosomal bodies</term>
<term>Lysosomal enzyme activities</term>
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<term>Other cells</term>
<term>Other conditions</term>
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<term>Present study</term>
<term>Senescent cells</term>
<term>Serial subcultures</term>
<term>Starter cultures</term>
<term>Takahashi</term>
<term>Transpeptidase</term>
<term>Transpeptidase activity</term>
<term>Triplicate samples</term>
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<div type="abstract" xml:lang="en">γ‐Glutamyl transpeptidase has multi‐catalytic activities. It degrades glutathi‐one and can produce ammmonia from glutamine. The present study was designed to examine whether the decreased cell proliferation, cellular gluta‐thione content and concurrent increase in ammonia production in senescent cells in culture are the result of increased γ‐glutamyl transpeptidase activity. We used IMR‐90 fibroblast and 3T3 LI preadipocyte cultures. The cellular glutathione content depended upon cell proliferation and cell density. The glutathione content was higher in cells at logarithmic growth, and lower at stationary growth or post confluency; dead cells had no detectable glutathione by the method currently used. The glutathione content was minimal in “old” IMR‐90 cells, regardless of cell density. On the other hand, an increase occurred in the unit number of molecules of bound 5‐iodoacetoamidofluorescein, an active‐site directed stoichiometric inhibitor of transpeptidase. That result corresponded favorably with the increased enzyme activity, suggesting that the number of enzyme molecules per cell was increased. The inhibition of ammonia production of the cultures by inhibition of γ‐glutamyl transpeptidase by 5‐iodoacetoamidofluorescein and reversible inhibition of ammonia production by a serine‐borate mixture were consistent with our postulate. Addition of NH4Cl (0.1 mM) to IMR‐90 cultures caused increased activities of transpeptidase and some of the lysosomal enzymes; concurrently, the amount of cellular glutathione and the number of cell divisions decreased. This suggests that the increased ammonia production presumably resulting from glutaminase activity of the observed increase of transpeptidase may profoundly affect certain cellular functions.</div>
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