TY - JOUR
T1 - A light and electron microscopic study of calcitonin gener-related peptide in the spinal cord of the rat
AU - McNeill, Daniel L.
AU - Coggeshall, Richard E.
AU - Carlton, Susan M.
N1 - Funding Information:
tron microscope. ’ We appreciate the generosity of Dr. Cary Cooper for the CGRP antibody. We thank Cindy Do for her excellent technical assistance and Lavem Wilson for her efficient typing of the manuscript. This study was supported by grants NS 11255, NS 10 I6 1, NS07 185 from the National Institutes of Health and by the Florence and Marie Hall Endowment for Excellence in Medical Education. Please address reprint requests to S.M.C.. Marine Biomedical Institute, Univ. of Texas Medical Branch, Galveston, TX 77550.
PY - 1988/3
Y1 - 1988/3
N2 - The present study localized calcitonin gene-related peptide at the light and electron microscopic levels in the lumbar spinal cord of the rat. One finding was that axons and terminals were labeled in both lamina I and Ilo medially but only in lamina I laterally. The functional implications of this innervation pattern are not clear but presumably this anatomic arrangement bears on both dorsoventral and mediolateral patterns of organization of primary afferent input into the dorsal horn. We also found that although the means of labeled myelinated and unmyelinated axon diameters in the tract of Lissauer were different, there was great overlap in these populations. Furthermore, subcellular localizations indicated that immunostaining of calcitonin gene-related peptide was associated primarily with microtubules in axons and cores of large dense-core vesicles in presynaptic terminals. Finally, labeled presynaptic terminals contained relatively few large dense-core vesicles and formed the presynaptic elements of simple axodendritic contacts almost exclusively. These last findings contrast with localizations of calcitonin gene-related peptide in the monkey, which has many more large dense-core vesicles in labeled terminals and in which a much higher proportion of labeled endings form the central parts of glomeruli.
AB - The present study localized calcitonin gene-related peptide at the light and electron microscopic levels in the lumbar spinal cord of the rat. One finding was that axons and terminals were labeled in both lamina I and Ilo medially but only in lamina I laterally. The functional implications of this innervation pattern are not clear but presumably this anatomic arrangement bears on both dorsoventral and mediolateral patterns of organization of primary afferent input into the dorsal horn. We also found that although the means of labeled myelinated and unmyelinated axon diameters in the tract of Lissauer were different, there was great overlap in these populations. Furthermore, subcellular localizations indicated that immunostaining of calcitonin gene-related peptide was associated primarily with microtubules in axons and cores of large dense-core vesicles in presynaptic terminals. Finally, labeled presynaptic terminals contained relatively few large dense-core vesicles and formed the presynaptic elements of simple axodendritic contacts almost exclusively. These last findings contrast with localizations of calcitonin gene-related peptide in the monkey, which has many more large dense-core vesicles in labeled terminals and in which a much higher proportion of labeled endings form the central parts of glomeruli.
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U2 - 10.1016/0014-4886(88)90186-0
DO - 10.1016/0014-4886(88)90186-0
M3 - Article
C2 - 3257735
AN - SCOPUS:0023901384
SN - 0014-4886
VL - 99
SP - 699
EP - 708
JO - Experimental Neurology
JF - Experimental Neurology
IS - 3
ER -