?2A-adrenergic receptors are expressed by diverse cell types in the fetal primate cerebral wall
✍ Scribed by Wang, Feng; Lidow, Michael S.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 680 KB
- Volume
- 378
- Category
- Article
- ISSN
- 0021-9967
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✦ Synopsis
The cellular elements of the fetal monkey cerebral wall expressing a2A, the most common subtype of the a2 receptor class, were examined by using nonisotopic in situ hybridization and immunohistochemistry with double-labeling for cell type-specific markers. At the three embryonic ages examined, E70, E90, and E120, a2A receptors were expressed throughout the embryonic cerebral wall. In the E70 and E90 fetuses, a2A receptors were observed in most cells of the proliferative zones. Some a2A-positive cells also expressed a proliferationassociated antigen, Ki-67, suggesting that the receptors are present in dividing cells. Furthermore, at E90, a2A receptors were detected on fibers passing between the ventricular and subventricular proliferative zones. At all ages studied, a2A receptors were expressed by migrating neurons in the intermediate zone, characterized by a spindle-like shape, radial alignment, and close association with radial glia. a2A receptors were also expressed by postmigrational microtubule-associated protein-2-positive neurons of the intermediate and subplate zones and the cortical plate. In the marginal zone, a2A receptors were present in the Cajal-Retzius neurons. Finally, a2A receptors were seen in the glial fibrillary acidic proteinpositive cells at all ages studied. In addition, dopamine-b-hydroxylase immunohistochemistry, employed to determine the potential source of noradrenaline in the embryonic cerebral wall, revealed noradrenergic innervation in the marginal, subplate, and intermediate zones of the monkey occipital lobe as early as E70. Based on our observations and available data on a2A signal transduction pathways, we propose that these receptors are involved in regulating the generation, migration, and maturation of cerebral cortical cells.