GDNF family ligand receptor components Ret and GFRalpha-1 in the human trigeminal ganglion and sensory nuclei
The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GF...
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Published in | Brain research bulletin Vol. 69; no. 4; pp. 393 - 403 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
28.04.2006
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Subjects | |
Online Access | Get full text |
ISSN | 0361-9230 1873-2747 |
DOI | 10.1016/j.brainresbull.2006.02.003 |
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Abstract | The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret
+ and GFRalpha-1
+ trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret
+ are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1
+ cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret
+/GDNF
+/GFRalpha-1
+ neurons, but also a number of Ret
−/GDNF
+/GFRalpha-1
+ and Ret
+/GDNF
−/GFRalpha-1
+ cells. Both Ret
+ and GFRalpha-1
+ neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret
+ pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret
+ nerve fibers and puncta gather in the inner substantia gelatinosa. Ret
+ neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1
+-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal. |
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AbstractList | The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret
+ and GFRalpha-1
+ trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret
+ are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1
+ cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret
+/GDNF
+/GFRalpha-1
+ neurons, but also a number of Ret
−/GDNF
+/GFRalpha-1
+ and Ret
+/GDNF
−/GFRalpha-1
+ cells. Both Ret
+ and GFRalpha-1
+ neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret
+ pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret
+ nerve fibers and puncta gather in the inner substantia gelatinosa. Ret
+ neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1
+-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal. The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret super(+) and GFRalpha-1 super(+) trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret super(+) are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1 super(+) cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret super(+)/GDNF super(+)/GFRalpha-1 super(+) neurons, but also a number of Ret super(-)/GDNF super(+)/GFRalpha-1 super(+) and Ret super(+)/GDNF super(-)/GFRalpha- 1 super(+) cells. Both Ret super(+) and GFRalpha-1 super(+) neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret super(+) pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret super(+) nerve fibers and puncta gather in the inner substantia gelatinosa. Ret super(+) neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1 super(+)-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal. The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret+ and GFRalpha-1+ trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret+ are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1+ cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret+/GDNF+/GFRalpha-1+ neurons, but also a number of Ret-/GDNF+/GFRalpha-1+ and Ret+/GDNF-/GFRalpha-1+ cells. Both Ret+ and GFRalpha-1+ neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret+ pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret+ nerve fibers and puncta gather in the inner substantia gelatinosa. Ret+ neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1+-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal. The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret+ and GFRalpha-1+ trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret+ are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1+ cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret+/GDNF+/GFRalpha-1+ neurons, but also a number of Ret-/GDNF+/GFRalpha-1+ and Ret+/GDNF-/GFRalpha-1+ cells. Both Ret+ and GFRalpha-1+ neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret+ pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret+ nerve fibers and puncta gather in the inner substantia gelatinosa. Ret+ neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1+-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal.The occurrence of Ret and GFRalpha-1 receptors is shown by immunohistochemistry in the human trigeminal sensory system at pre-, postnatal and adult age. Receptor-labeled neurons occur in both trigeminal ganglion and mesencephalic nucleus. In adult trigeminal ganglion, about 75% of Ret- and 65% of GFRalpha-1-labeled neurons are small- and medium-sized. The proportion of Ret+ and GFRalpha-1+ trigeminal ganglion neurons in the adult is about 25 and 60%, respectively. The majority of Ret+ are double labeled for GFRalpha-1 and glial cell line-derived neurotrophic factor (GDNF). Most of the GFRalpha-1+ cells contain GDNF and about 50% of them contain Ret. Triple labeling shows many Ret+/GDNF+/GFRalpha-1+ neurons, but also a number of Ret-/GDNF+/GFRalpha-1+ and Ret+/GDNF-/GFRalpha-1+ cells. Both Ret+ and GFRalpha-1+ neuronal subpopulations overlap with that containing calcitonin gene-related peptide. Ret+ pericellular basket-like nerve fibers occur in the adult trigeminal ganglion. Centrally, immunoreactivity is restricted to the spinal nucleus pars caudalis and pars interpolaris and to the mesencephalic nucleus. In adult specimens, Ret+ nerve fibers and puncta gather in the inner substantia gelatinosa. Ret+ neurons occur in the spinal nucleus and are more frequent in newborn than in adult subjects. Central GFRalpha-1+-labeled neurons and punctate elements are sparse. These findings support the involvement of GDNF and possibly other cognate ligands in the trophism of human trigeminal primary sensory neurons from prenatal life to adulthood, indicating a selective commitment to cells devoted to protopathic and proprioceptive sensory transmission. They also support the possibility that receptor molecules other than Ret could be active in transducing the ligand signal. |
Author | Boi, Marianna Del Fiacco, Marina Quartu, Marina Lai, Maria Letizia Mascia, Francesca Serra, Maria Pina Spano, Alessia |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/16624671$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_brainres_2007_01_065 crossref_primary_10_1186_1744_8069_7_5 crossref_primary_10_1016_j_brainresrev_2007_08_009 crossref_primary_10_1177_0333102417695105 crossref_primary_10_1007_s11055_015_0094_8 crossref_primary_10_1016_j_brainres_2007_07_064 crossref_primary_10_1111_j_1469_7580_2010_01254_x crossref_primary_10_1134_S2079057014030047 crossref_primary_10_1016_j_neulet_2011_07_047 crossref_primary_10_1016_j_bbi_2009_08_002 crossref_primary_10_1016_j_bbi_2012_10_023 |
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Keywords | Colocalization Trigeminal sensory system GDNF receptors Development Man Adulthood CGRP |
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SubjectTerms | Adult Adulthood Aged Aged, 80 and over Calcitonin Gene-Related Peptide - metabolism CGRP Colocalization Development Fetus - metabolism GDNF receptors Glial Cell Line-Derived Neurotrophic Factor - metabolism Glial Cell Line-Derived Neurotrophic Factor Receptors - metabolism Humans Immunohistochemistry Infant Infant, Newborn Man Middle Aged Proto-Oncogene Proteins c-ret - metabolism Trigeminal Ganglion - embryology Trigeminal Ganglion - growth & development Trigeminal Ganglion - metabolism Trigeminal Nuclei - embryology Trigeminal Nuclei - growth & development Trigeminal Nuclei - metabolism Trigeminal sensory system |
Title | GDNF family ligand receptor components Ret and GFRalpha-1 in the human trigeminal ganglion and sensory nuclei |
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