Oligodendrocytes express gap junction proteins connexin32 and connexin45

• Published in: Glia Vol. 20; no. 2; pp. 101 - 114
• Main Authors: Dermietzel, R., Farooq, M., Kessler, J.A., Althaus, H., Hertzberg, E.L., Spray, D.C.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 01.06.1997; Wiley-Liss
• Subjects: Animals; Biological and medical sciences; Brain - cytology; Brain - physiology; Cattle; Cells, Cultured; connexin32; connexin45; Connexins - analysis; Connexins - biosynthesis; DNA Primers; Electric Conductivity; electrical coupling; Fundamental and applied biological sciences. Psychology; gap junction; Gap Junction beta-1 Protein; Gap Junctions - physiology; Gap Junctions - ultrastructure; Isolated neuron and nerve. Neuroglia; Membrane Potentials; Myelin Sheath - physiology; Myelin Sheath - ultrastructure; oligodendrocytes; Oligodendroglia - cytology; Oligodendroglia - physiology; Patch-Clamp Techniques; Polymerase Chain Reaction; Swine; Vertebrates: nervous system and sense organs; Neuroglia; Central nervous system; Cell junction; Ox; Gene expression; In vitro; Gap junction; Pig; Proteins; Connexin; Vertebrata; Mammalia; Oligodendrocyte; Artiodactyla; Ungulata; Brain (vertebrata)
• ISSN: 0894-1491; 1098-1136
• DOI: 10.1002/(SICI)1098-1136(199706)20:2<101::AID-GLIA2>3.0.CO;2-C

Oligodendrocytes, the myelin‐forming glia of brain, are connected by gap junctions in situ and in culture. Cultured oligodendrocytes from adult bovine and porcine brains were studied using immunocytochemical, molecular, and electrophysiological techniques in order to characterize the gap junction types. The expression of connexin32 was substantiated by the detection of low, but significant, signals using connexin‐specific probes in Northern and Western blot analyses. Connexin43, which comprises gap junctions in astrocytes, was not detectable in pure oligodendrocytic cultures; mRNAs of connexin40 and connexin37 and connexin26 were also not detected. By means of two specific antibodies directed to the recently cloned connexin45 and by RT‐PCR we were able to identify this connexin as a second oligodendrocytic gap junction protein. Whole cell voltage clamp recording provided evidence for electrical coupling between pairs of cultured oligodendrocytes (mean junctional conductance 3.9 nS, n = 38 pairs) and intracellular Lucifer Yellow injection indicated that oligodendrocytes were usually only weakly dye coupled, with spread generally being restricted to nearest neighbors. Unitary conductances ranged from >20 to <150 pS with modes of distribution at about 100 to 120pS and 40 to 20 pS, respectively. These unitary conductances are consistent with the channel events expected for connexin32 and connexin45. The low degree of functional coupling between oligodendrocytes in vitro corresponds with the low levels of connexin32 and connexin45 messenger RNAs and protein expression. GLIA 20:101‐114, 1997. © 1997 Wiley‐Liss Inc.