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Modulation of glial glutamate transport through cell interactions with the extracellular matrix
Author(s) -
Ye ZuCheng,
Sontheimer Harald
Publication year - 2002
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/s0736-5748(02)00048-5
Subject(s) - glutamate receptor , glutamate aspartate transporter , microbiology and biotechnology , astrocyte , extracellular matrix , biology , extracellular , chemistry , biochemistry , central nervous system , neuroscience , metabotropic glutamate receptor , receptor
Glial glutamate transport plays a pivotal role in maintaining glutamate homeostasis in the central nervous system. Expression of glutamate transporters is highly regulated during brain development, and a number of pathological conditions are associated with deficits in expression and/or function of glutamate transports. While several soluble factors have been shown to regulate the expression of glutamate transporter, the contribution of cell–cell interaction and cell–environmental interaction in the regulation of glutamate transport is unknown. Extracellular matrix (ECM) molecules are essential components in cell–cell and cell–environmental interactions, and the ECM has been shown to play critical role in normal development and during brain pathogenesis. We, therefore, investigated the possibility that ECM molecules may regulate astrocytic glutamate transport. Therefore, we cultured rat cortical astrocytes with different ECMs and determined expression levels of the two astrocytic glutamate transporters GLT‐1 and GLAST by Western Blot and determined transporter activity through measurements of 3 H‐ d ‐aspartate uptake. Astrocytes grown on poly‐ornithine or poly‐ d / l ‐lysine showed approximately two‐fold higher GLT‐1 expression than sister cells grown on plastic dishes without ECM. Naturally occurring ECM's, including laminin and collagen, showed a dose‐dependent regulation of GLT‐1 protein expression. These effects were specific for GLT‐1 as GLAST expression was unaffected by different ECMs. Surprisingly, however, none of the examined ECMs altered the apparent glutamate uptake activity. In probing blots side‐by‐side for expression of Na + /K + ‐ATPase, we found that ECMs affected expression of Na + /K + ‐ATPase and GLT‐1 in a reciprocal fashion. Poly‐ornithine, for example, enhanced GLT‐1 expression, but reduced expression of Na + /K + ‐ATPase. Na + transport may, thus, be a limiting factor for glutamate uptake.