Cargando…
Evidence of primary cilia in the developing rat heart
BACKGROUND: A transient increase in cytosolic Ca(2+) (the “Ca(2+) transient”) determines the degree and duration of myocyte force development in the heart. However, we have previously observed that, under the same experimental conditions, the Ca(2+) transients from isolated cardiac myocytes are redu...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069708/ https://www.ncbi.nlm.nih.gov/pubmed/30079247 http://dx.doi.org/10.1186/s13630-018-0058-z |
_version_ | 1783343551753486336 |
---|---|
author | Kaur, Sarbjot McGlashan, Sue R. Ward, Marie-Louise |
author_facet | Kaur, Sarbjot McGlashan, Sue R. Ward, Marie-Louise |
author_sort | Kaur, Sarbjot |
collection | PubMed |
description | BACKGROUND: A transient increase in cytosolic Ca(2+) (the “Ca(2+) transient”) determines the degree and duration of myocyte force development in the heart. However, we have previously observed that, under the same experimental conditions, the Ca(2+) transients from isolated cardiac myocytes are reduced in amplitude in comparison to those from multicellular cardiac preparations. We therefore questioned whether the enzymatic cell isolation procedure might remove structures that modulate intracellular Ca(2+) in some way. Primary cilia are found in a diverse range of cell types, and have an abundance of Ca(2+)-permeable membrane channels that result in Ca(2+) influx when activated. Although primary cilia are reportedly ubiquitous, their presence and function in the heart remain controversial. If present, we hypothesized they might provide an additional Ca(2+) entry pathway in multicellular cardiac tissue that was lost during cell isolation. The aim of our study was to look for evidence of primary cilia in isolated myocytes and ventricular tissue from rat hearts. METHODS: Immunohistochemical techniques were used to identify primary cilia-specific proteins in isolated myocytes from adult rat hearts, and in tissue sections from embryonic, neonatal, young, and adult rat hearts. Either mouse anti-acetylated α-tubulin or rabbit polyclonal ARL13B antibodies were used, counterstained with Hoechst dye. Selected sections were also labelled with markers for other cell types found in the heart and for myocyte F-actin. RESULTS: No evidence of primary cilia was found in either tissue sections or isolated myocytes from adult rat ventricles. However, primary cilia were present in tissue sections from embryonic, neonatal (P2) and young (P21 and P28) rat hearts. CONCLUSION: The lack of primary cilia in adult rat hearts rules out their contribution to myocyte Ca(2+) homoeostasis by providing a Ca(2+) entry pathway. However, evidence of primary cilia in tissue from embryonic and very young rat hearts suggests they have a role during development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13630-018-0058-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6069708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60697082018-08-03 Evidence of primary cilia in the developing rat heart Kaur, Sarbjot McGlashan, Sue R. Ward, Marie-Louise Cilia Short Report BACKGROUND: A transient increase in cytosolic Ca(2+) (the “Ca(2+) transient”) determines the degree and duration of myocyte force development in the heart. However, we have previously observed that, under the same experimental conditions, the Ca(2+) transients from isolated cardiac myocytes are reduced in amplitude in comparison to those from multicellular cardiac preparations. We therefore questioned whether the enzymatic cell isolation procedure might remove structures that modulate intracellular Ca(2+) in some way. Primary cilia are found in a diverse range of cell types, and have an abundance of Ca(2+)-permeable membrane channels that result in Ca(2+) influx when activated. Although primary cilia are reportedly ubiquitous, their presence and function in the heart remain controversial. If present, we hypothesized they might provide an additional Ca(2+) entry pathway in multicellular cardiac tissue that was lost during cell isolation. The aim of our study was to look for evidence of primary cilia in isolated myocytes and ventricular tissue from rat hearts. METHODS: Immunohistochemical techniques were used to identify primary cilia-specific proteins in isolated myocytes from adult rat hearts, and in tissue sections from embryonic, neonatal, young, and adult rat hearts. Either mouse anti-acetylated α-tubulin or rabbit polyclonal ARL13B antibodies were used, counterstained with Hoechst dye. Selected sections were also labelled with markers for other cell types found in the heart and for myocyte F-actin. RESULTS: No evidence of primary cilia was found in either tissue sections or isolated myocytes from adult rat ventricles. However, primary cilia were present in tissue sections from embryonic, neonatal (P2) and young (P21 and P28) rat hearts. CONCLUSION: The lack of primary cilia in adult rat hearts rules out their contribution to myocyte Ca(2+) homoeostasis by providing a Ca(2+) entry pathway. However, evidence of primary cilia in tissue from embryonic and very young rat hearts suggests they have a role during development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13630-018-0058-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-31 /pmc/articles/PMC6069708/ /pubmed/30079247 http://dx.doi.org/10.1186/s13630-018-0058-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Kaur, Sarbjot McGlashan, Sue R. Ward, Marie-Louise Evidence of primary cilia in the developing rat heart |
title | Evidence of primary cilia in the developing rat heart |
title_full | Evidence of primary cilia in the developing rat heart |
title_fullStr | Evidence of primary cilia in the developing rat heart |
title_full_unstemmed | Evidence of primary cilia in the developing rat heart |
title_short | Evidence of primary cilia in the developing rat heart |
title_sort | evidence of primary cilia in the developing rat heart |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069708/ https://www.ncbi.nlm.nih.gov/pubmed/30079247 http://dx.doi.org/10.1186/s13630-018-0058-z |
work_keys_str_mv | AT kaursarbjot evidenceofprimaryciliainthedevelopingratheart AT mcglashansuer evidenceofprimaryciliainthedevelopingratheart AT wardmarielouise evidenceofprimaryciliainthedevelopingratheart |