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Journal of Neuroscience, Vol 11, 1421-1432, Copyright © 1991 by Society for Neuroscience
Gap junctions between cultured astrocytes: immunocytochemical, molecular, and electrophysiological analysis
R Dermietzel, EL Hertberg, JA Kessler and DC Spray
Department of Anatomy, University of Regensburg, Germany.
The properties of astroglial gap junction channels and the protein that
constitutes the channels were characterized by immunocytochemical,
molecular biological, and physiological techniques. Comparative
immunocytochemical labeling utilizing different antibodies specific for
liver connexin 32 and connexin 26 and antibodies to peptides corresponding
to carboxy-terminal sequences of the heart gap junction protein (connexin
43) indicates that the predominant gap junction protein in astrocytes is
connexin 43. The expression of this connexin in cultured astrocytes was
also established by Western and Northern blot analyses. Cultured astrocytes
expressed connexin 43 mRNA and did not contain detectable levels of the
mRNAs encoding connexin 32 or connexin 26. Further, the cells contained the
same primary connexin 43 translation product and the same phosphorylated
forms as heart. Finally, electrophysiological recordings under
voltage-clamp conditions revealed that astrocyte cell pairs were moderately
well coupled, with an average junctional conductance of about 13 nS.
Single-channel recordings indicated a unitary junctional conductance of
about 50-60 pS, which is of the same order as that found in cultured rat
cardiac myocytes, where the channel properties of connexin 43 were first
described. Thus, physiological properties of gap junction channels appear
to be determined by the connexin expressed, independent of the tissue type.
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