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Calbindin D28k-Immunoreactivity in Human Enteric Neurons
Calbindin (CALB) is well established as immunohistochemical marker for intrinsic primary afferent neurons in the guinea pig gut. Its expression by numerous human enteric neurons has been demonstrated but little is known about particular types of neurons immunoreactive for CALB. Here we investigated...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796143/ https://www.ncbi.nlm.nih.gov/pubmed/29316719 http://dx.doi.org/10.3390/ijms19010194 |
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author | Zetzmann, Katharina Strehl, Johanna Geppert, Carol Kuerten, Stefanie Jabari, Samir Brehmer, Axel |
author_facet | Zetzmann, Katharina Strehl, Johanna Geppert, Carol Kuerten, Stefanie Jabari, Samir Brehmer, Axel |
author_sort | Zetzmann, Katharina |
collection | PubMed |
description | Calbindin (CALB) is well established as immunohistochemical marker for intrinsic primary afferent neurons in the guinea pig gut. Its expression by numerous human enteric neurons has been demonstrated but little is known about particular types of neurons immunoreactive for CALB. Here we investigated small and large intestinal wholemount sets of 26 tumor patients in order to evaluate (1) the proportion of CALB(+) neurons in the total neuron population, (2) the colocalization of CALB with calretinin (CALR), somatostatin (SOM) and vasoactive intestinal peptide (VIP) and (3) the morphology of CALB(+) neurons. CALB(+) neurons represented a minority of myenteric neurons (small intestine: 31%; large intestine: 25%) and the majority of submucosal neurons (between 72 and 95%). In the submucosa, most CALB(+) neurons co-stained for CALR and VIP (between 69 and 80%) or for SOM (between 20 and 3%). In the myenteric plexus, 85% of CALB(+) neurons did not co-stain with the other markers investigated. An unequivocal correlation between CALB reactivity and neuronal morphology was found for myenteric type III neurons in the small intestine: uniaxonal neurons with long, slender and branched dendrites were generally positive for CALB. Since also other neurons displayed occasional CALB reactivity, this protein is not suited as an exclusive marker for type III neurons. |
format | Online Article Text |
id | pubmed-5796143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57961432018-02-09 Calbindin D28k-Immunoreactivity in Human Enteric Neurons Zetzmann, Katharina Strehl, Johanna Geppert, Carol Kuerten, Stefanie Jabari, Samir Brehmer, Axel Int J Mol Sci Article Calbindin (CALB) is well established as immunohistochemical marker for intrinsic primary afferent neurons in the guinea pig gut. Its expression by numerous human enteric neurons has been demonstrated but little is known about particular types of neurons immunoreactive for CALB. Here we investigated small and large intestinal wholemount sets of 26 tumor patients in order to evaluate (1) the proportion of CALB(+) neurons in the total neuron population, (2) the colocalization of CALB with calretinin (CALR), somatostatin (SOM) and vasoactive intestinal peptide (VIP) and (3) the morphology of CALB(+) neurons. CALB(+) neurons represented a minority of myenteric neurons (small intestine: 31%; large intestine: 25%) and the majority of submucosal neurons (between 72 and 95%). In the submucosa, most CALB(+) neurons co-stained for CALR and VIP (between 69 and 80%) or for SOM (between 20 and 3%). In the myenteric plexus, 85% of CALB(+) neurons did not co-stain with the other markers investigated. An unequivocal correlation between CALB reactivity and neuronal morphology was found for myenteric type III neurons in the small intestine: uniaxonal neurons with long, slender and branched dendrites were generally positive for CALB. Since also other neurons displayed occasional CALB reactivity, this protein is not suited as an exclusive marker for type III neurons. MDPI 2018-01-08 /pmc/articles/PMC5796143/ /pubmed/29316719 http://dx.doi.org/10.3390/ijms19010194 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zetzmann, Katharina Strehl, Johanna Geppert, Carol Kuerten, Stefanie Jabari, Samir Brehmer, Axel Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title | Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title_full | Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title_fullStr | Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title_full_unstemmed | Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title_short | Calbindin D28k-Immunoreactivity in Human Enteric Neurons |
title_sort | calbindin d28k-immunoreactivity in human enteric neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796143/ https://www.ncbi.nlm.nih.gov/pubmed/29316719 http://dx.doi.org/10.3390/ijms19010194 |
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