Immunohistochemical distribution of delta opioid receptors in the rat central nervous system: Evidence for somatodendritic labeling and antigen-specific cellular compartmentalization

被引:109
作者
Cahill, CM
McClellan, KA
Morinville, A
Hoffert, C
Hubatsch, D
O'Donnell, D
Beaudet, A
机构
[1] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3A 2B4, Canada
[3] AstraZeneca R&D, Montreal, PQ H3A 1A1, Canada
关键词
immunohistochemistry; electron microscopy; opiate; brain; spinal cord;
D O I
10.1002/cne.1370
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many studies have reported on the distribution of delta opioid receptors (delta OR) in the mammalian central nervous system (CNS) by using a variety of techniques. However, no general consensus has emerged with regards to the localization of this receptor due to inconsistencies in the immunohistochemical literature. In the present study, we analyzed the cellular and subcellular distribution of immunoreactive delta OR in the rat CNS using two different antibodies (directed against a sequence in the C-terminus or N-terminus of the rat delta OR). By using Western blotting, these two antibodies recognized similar forms of the delta OR in COS-7 cells transfected with this receptor, but distinct forms in membranes from the rat spinal cord. By using light microscopic immunohistochemistry, both antibodies recognized identical populations of nerve cell bodies throughout the CNS; the distribution of these cell bodies conformed to that of delta OR mRNA-expressing cells detected by in situ hybridization. However, whereas the C-terminus-directed antibody recognized predominantly perikarya and proximal dendrites, the N-terminus-directed antibody also labeled extensively dendritic and terminal arbors. Furthermore, by using electron microscopy, the two antibodies were found not only to label differentially somatodendritic versus axonal compartments, but also plasma membrane versus cytoplasmic ones, suggesting that distinct immunological forms of the receptor are being targeted preferentially to different cellular and subcellular domains. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:65 / 84
页数:20
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