Regulation of acetylated tubulin/Na +,K +-ATPase interaction by l-glutamate in non-neural cells: involvement of microtubules
A subpopulation of membrane tubulin consisting mainly of the acetylated isotype is associated with Na +,K +-ATPase and inhibits the enzyme activity. We found recently that treatment of cultured astrocytes with l-glutamate induces dissociation of the acetylated tubulin/Na +,K +-ATPase complex, result...
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Published in | Biochimica et biophysica acta Vol. 1721; no. 1; pp. 185 - 192 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
18.01.2005
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Subjects | |
Online Access | Get full text |
ISSN | 0304-4165 0006-3002 1872-8006 |
DOI | 10.1016/j.bbagen.2004.11.003 |
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Summary: | A subpopulation of membrane tubulin consisting mainly of the acetylated isotype is associated with Na
+,K
+-ATPase and inhibits the enzyme activity. We found recently that treatment of cultured astrocytes with
l-glutamate induces dissociation of the acetylated tubulin/Na
+,K
+-ATPase complex, resulting in increased enzyme activity. We now report occurrence of this phenomenon in non-neural cells. As in the case of astrocytes, the effect of
l-glutamate is mediated by its transporters and not by specific receptors. In COS cells, the effect of
l-glutamate was reversed by its elimination from culture medium, provided that
d-glucose was present. The effect of
l-glutamate was not observed when Na
+ was replaced by K
+ in the incubation medium. The ionophore monensin, in the presence of Na
+, had the same effect as
l-glutamate. Treatment of cells with taxol prevented the dissociating effect of
l-glutamate or monensin. Nocodazole treatment of intact cells or isolated membranes dissociated the acetylated tubulin/Na
+,K
+-ATPase complex. The dissociating effect of nocodazol does not require Na
+. These results indicate a close functional relationship among Na
+,K
+-ATPase, microtubules, and
l-glutamate transporters, and a possible role in cell signaling pathways. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0304-4165 0006-3002 1872-8006 |
DOI: | 10.1016/j.bbagen.2004.11.003 |