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Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development

BACKGROUND: Adrenal chromaffin cells and sympathetic neurons both originate from the neural crest, yet signals that trigger chromaffin development remain elusive. Bone morphogenetic proteins (BMPs) emanating from the dorsal aorta are important signals for the induction of a sympathoadrenal catechola...

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Autores principales: Huber, Katrin, Franke, Aylin, Brühl, Barbara, Krispin, Shlomi, Ernsberger, Uwe, Schober, Andreas, Halbach, Oliver von Bohlen und, Rohrer, Hermann, Kalcheim, Chaya, Unsicker, Klaus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582231/
https://www.ncbi.nlm.nih.gov/pubmed/18945349
http://dx.doi.org/10.1186/1749-8104-3-28
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author Huber, Katrin
Franke, Aylin
Brühl, Barbara
Krispin, Shlomi
Ernsberger, Uwe
Schober, Andreas
Halbach, Oliver von Bohlen und
Rohrer, Hermann
Kalcheim, Chaya
Unsicker, Klaus
author_facet Huber, Katrin
Franke, Aylin
Brühl, Barbara
Krispin, Shlomi
Ernsberger, Uwe
Schober, Andreas
Halbach, Oliver von Bohlen und
Rohrer, Hermann
Kalcheim, Chaya
Unsicker, Klaus
author_sort Huber, Katrin
collection PubMed
description BACKGROUND: Adrenal chromaffin cells and sympathetic neurons both originate from the neural crest, yet signals that trigger chromaffin development remain elusive. Bone morphogenetic proteins (BMPs) emanating from the dorsal aorta are important signals for the induction of a sympathoadrenal catecholaminergic cell fate. RESULTS: We report here that BMP-4 is also expressed by adrenal cortical cells throughout chick embryonic development, suggesting a putative role in chromaffin cell development. Moreover, bone morphogenetic protein receptor IA is expressed by both cortical and chromaffin cells. Inhibiting BMP-4 with noggin prevents the increase in the number of tyrosine hydroxylase positive cells in adrenal explants without affecting cell proliferation. Hence, adrenal BMP-4 is likely to induce tyrosine hydroxylase in sympathoadrenal progenitors. To investigate whether persistent BMP-4 exposure is able to induce chromaffin traits in sympathetic ganglia, we locally grafted BMP-4 overexpressing cells next to sympathetic ganglia. Embryonic day 8 chick sympathetic ganglia, in addition to principal neurons, contain about 25% chromaffin-like cells. Ectopic BMP-4 did not increase this proportion, yet numbers and sizes of 'chromaffin' granules were significantly increased. CONCLUSION: BMP-4 may serve to promote specific chromaffin traits, but is not sufficient to convert sympathetic neurons into a chromaffin phenotype.
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spelling pubmed-25822312008-11-12 Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development Huber, Katrin Franke, Aylin Brühl, Barbara Krispin, Shlomi Ernsberger, Uwe Schober, Andreas Halbach, Oliver von Bohlen und Rohrer, Hermann Kalcheim, Chaya Unsicker, Klaus Neural Develop Research Article BACKGROUND: Adrenal chromaffin cells and sympathetic neurons both originate from the neural crest, yet signals that trigger chromaffin development remain elusive. Bone morphogenetic proteins (BMPs) emanating from the dorsal aorta are important signals for the induction of a sympathoadrenal catecholaminergic cell fate. RESULTS: We report here that BMP-4 is also expressed by adrenal cortical cells throughout chick embryonic development, suggesting a putative role in chromaffin cell development. Moreover, bone morphogenetic protein receptor IA is expressed by both cortical and chromaffin cells. Inhibiting BMP-4 with noggin prevents the increase in the number of tyrosine hydroxylase positive cells in adrenal explants without affecting cell proliferation. Hence, adrenal BMP-4 is likely to induce tyrosine hydroxylase in sympathoadrenal progenitors. To investigate whether persistent BMP-4 exposure is able to induce chromaffin traits in sympathetic ganglia, we locally grafted BMP-4 overexpressing cells next to sympathetic ganglia. Embryonic day 8 chick sympathetic ganglia, in addition to principal neurons, contain about 25% chromaffin-like cells. Ectopic BMP-4 did not increase this proportion, yet numbers and sizes of 'chromaffin' granules were significantly increased. CONCLUSION: BMP-4 may serve to promote specific chromaffin traits, but is not sufficient to convert sympathetic neurons into a chromaffin phenotype. BioMed Central 2008-10-22 /pmc/articles/PMC2582231/ /pubmed/18945349 http://dx.doi.org/10.1186/1749-8104-3-28 Text en Copyright © 2008 Huber et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Huber, Katrin
Franke, Aylin
Brühl, Barbara
Krispin, Shlomi
Ernsberger, Uwe
Schober, Andreas
Halbach, Oliver von Bohlen und
Rohrer, Hermann
Kalcheim, Chaya
Unsicker, Klaus
Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title_full Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title_fullStr Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title_full_unstemmed Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title_short Persistent expression of BMP-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
title_sort persistent expression of bmp-4 in embryonic chick adrenal cortical cells and its role in chromaffin cell development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582231/
https://www.ncbi.nlm.nih.gov/pubmed/18945349
http://dx.doi.org/10.1186/1749-8104-3-28
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