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Astroglial cells in vitro are heterogeneous with respect to expression of the α 1 ‐adrenergic receptor
Author(s) -
Lerea Leslie S.,
McCarthy Ken D.
Publication year - 1989
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.440020302
Subject(s) - biology , in vitro , neuroscience , microbiology and biotechnology , receptor , adrenergic , astrocyte , expression (computer science) , central nervous system , genetics , computer science , programming language
A wide variety of approaches have been used to examine the expression of neuroligand receptors by cultured astroglial cells. The results of such studies make it clear that these cells exhibit most, if not all, of the different receptors known to be associated with central neurons. However, it has been more difficult to determine if there are multiple populations of astroglia that can be distinguished on the basis of their complement of neuroligand receptors. To address this question, we established a radioligand binding assay that enabled us to visualize α 1 ‐adrenergic receptors (α 1 ‐ARs) on immunocytochemically defined neural cells. Saturation, time course, and competition binding experiments determined that 125 I‐HEAT could be used to identify α 1 ‐AR binding sites on immunocytochemically defined astroglial cells. Our results indicate that approximately 66% of cortical polygonal astroglia express detectable numbers of α 1 ‐ARs. 3 H‐thymidine labeling experiments indicate that both dividing and nondividing astroglia exhibit α 1 ‐ARs. These results greatly contrast with studies on β‐adrenergic receptor expression (β‐AR), in which 100% of polygonal astroglia express β‐ARs. Process‐bearing astroglia also exhibit α 1 ‐ARs, which is in marked contrast to the lack of β‐AR expression by these cells. The results presented here suggest that astroglia, like neurons, differ in the receptors they express and therefore may be able to selectively respond to extracellular stimulation.

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