Distribution of mRNAs coding for liver and heart gap junction proteins in the rat central nervous system
- 1 March 1991
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 305 (1) , 96-118
- https://doi.org/10.1002/cne.903050110
Abstract
The present study examined the distributions of connexin43 mRNA and connexin32 mRNA in the central nervous system (CNS) of the rat by using in situ hybridization histochemistry. These connexins are the best studied gap junction proteins; connexin32 forms direct cell-cell channels in the liver, as does connexin43 in the heart. There was a differential distribution of cells containing connexin32 mRNA compared with the population of cells which contained connexin43 mRNA, thus implying a regional specificity in the expression of connexins in the CNS. Cells containing connexin43 mRNA were uniformly distributed throughout the gray matter of the neuraxis. Several areas had a higher concentration of cells that express connexin43, such as layer IA of the piriform cortex, supraoptic and paraventricular nuclei of the hypothalamus, anterior cortical amygdaloid nucleus, the reticular part of the substantia nigra, lateral habenula, mesencephalic trigeminal nucleus, Purkinje cell layer of the cerebellum, facial nucleus, prepositus hypoglossal nucleus, and dorsal cochlear nucleus. The pattern of connexin43 hybridization and the morphology of connexin43 mRNA containing cells suggest that this gap junction forming protein is found predominantly in astrocytes, Con-nexin32 mRNA was detected in discrete cell groups of the gray matter that appeared to be neurons, including cells in layer 2 of the neocortex, layer II of the piriform cortex, pyramidal cell layer of the hippocampus, granule and polymorphic cell layers of the dentate gyrus, islands of Calleja, olfactory tubercle, lateral thalamic nuclei, lateral habenula, and Purkinje cell layer of the cerebellar cortex. A large population of cells in white matter tracts that were labelled with the connexin32 riboprobe appeared to be oligodendrocytes. These studies suggest that neurons and glial cells express connexin32 mRNA, but only astrocytes express connexin43 mRNA. Many of the areas in which connexin mRNAs were demonstrated have electrically coupled cells, morphologically distinct gap junction plaques, and/or have immunocytochemically identifiable connexin proteins. These results indicate that cells with mRNAs coding for intercellular channels have a widespread distribution in the mammalian CNS.Keywords
This publication has 52 references indexed in Scilit:
- Regional differences in connexin32 and connexin43 messenger RNAs in rat brainNeuroscience Letters, 1990
- A 16 kDa protein co‐isolating with gap junctions from brain tissue belonging to the class of proteolipids of the vacuolar H+‐ATPasesFEBS Letters, 1989
- Formation of gap junctions by expression of connexins in Xenopus oocyte pairsCell, 1989
- Cloning and Expression of a Xenopus Embryonic Gap Junction ProteinScience, 1989
- Gene regulation by steroid hormonesJournal of Steroid Biochemistry, 1987
- Translation and functional expression of cell-cell channel mRNA inXenopus oocytesThe Journal of Membrane Biology, 1985
- Antibody Probes in the Study of Gap Junctional CommunicationAnnual Review of Physiology, 1985
- A protein homologous to the 27,000 dalton liver gap junction protein is present in a wide variety of species and tissuesCell, 1984
- The ultrastructure of isolated rat oligodendroglial cell culturesJournal of Neurocytology, 1982
- Induction of cell–cell channel formation by mRNANature, 1981