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SERCA directs cell migration and branching across species and germ layers
Branching morphogenesis underlies organogenesis in vertebrates and invertebrates, yet is incompletely understood. Here, we show that the sarco-endoplasmic reticulum Ca(2+) reuptake pump (SERCA) directs budding across germ layers and species. Clonal knockdown demonstrated a cell-autonomous role for S...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665464/ https://www.ncbi.nlm.nih.gov/pubmed/28821490 http://dx.doi.org/10.1242/bio.026039 |
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author | Bower, Danielle V. Lansdale, Nick Navarro, Sonia Truong, Thai V. Bower, Dan J. Featherstone, Neil C. Connell, Marilyn G. Al Alam, Denise Frey, Mark R. Trinh, Le A. Fernandez, G. Esteban Warburton, David Fraser, Scott E. Bennett, Daimark Jesudason, Edwin C. |
author_facet | Bower, Danielle V. Lansdale, Nick Navarro, Sonia Truong, Thai V. Bower, Dan J. Featherstone, Neil C. Connell, Marilyn G. Al Alam, Denise Frey, Mark R. Trinh, Le A. Fernandez, G. Esteban Warburton, David Fraser, Scott E. Bennett, Daimark Jesudason, Edwin C. |
author_sort | Bower, Danielle V. |
collection | PubMed |
description | Branching morphogenesis underlies organogenesis in vertebrates and invertebrates, yet is incompletely understood. Here, we show that the sarco-endoplasmic reticulum Ca(2+) reuptake pump (SERCA) directs budding across germ layers and species. Clonal knockdown demonstrated a cell-autonomous role for SERCA in Drosophila air sac budding. Live imaging of Drosophila tracheogenesis revealed elevated Ca(2+) levels in migratory tip cells as they form branches. SERCA blockade abolished this Ca(2+) differential, aborting both cell migration and new branching. Activating protein kinase C (PKC) rescued Ca(2+) in tip cells and restored cell migration and branching. Likewise, inhibiting SERCA abolished mammalian epithelial budding, PKC activation rescued budding, while morphogens did not. Mesoderm (zebrafish angiogenesis) and ectoderm (Drosophila nervous system) behaved similarly, suggesting a conserved requirement for cell-autonomous Ca(2+) signaling, established by SERCA, in iterative budding. |
format | Online Article Text |
id | pubmed-5665464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56654642017-11-07 SERCA directs cell migration and branching across species and germ layers Bower, Danielle V. Lansdale, Nick Navarro, Sonia Truong, Thai V. Bower, Dan J. Featherstone, Neil C. Connell, Marilyn G. Al Alam, Denise Frey, Mark R. Trinh, Le A. Fernandez, G. Esteban Warburton, David Fraser, Scott E. Bennett, Daimark Jesudason, Edwin C. Biol Open Research Article Branching morphogenesis underlies organogenesis in vertebrates and invertebrates, yet is incompletely understood. Here, we show that the sarco-endoplasmic reticulum Ca(2+) reuptake pump (SERCA) directs budding across germ layers and species. Clonal knockdown demonstrated a cell-autonomous role for SERCA in Drosophila air sac budding. Live imaging of Drosophila tracheogenesis revealed elevated Ca(2+) levels in migratory tip cells as they form branches. SERCA blockade abolished this Ca(2+) differential, aborting both cell migration and new branching. Activating protein kinase C (PKC) rescued Ca(2+) in tip cells and restored cell migration and branching. Likewise, inhibiting SERCA abolished mammalian epithelial budding, PKC activation rescued budding, while morphogens did not. Mesoderm (zebrafish angiogenesis) and ectoderm (Drosophila nervous system) behaved similarly, suggesting a conserved requirement for cell-autonomous Ca(2+) signaling, established by SERCA, in iterative budding. The Company of Biologists Ltd 2017-08-17 /pmc/articles/PMC5665464/ /pubmed/28821490 http://dx.doi.org/10.1242/bio.026039 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Bower, Danielle V. Lansdale, Nick Navarro, Sonia Truong, Thai V. Bower, Dan J. Featherstone, Neil C. Connell, Marilyn G. Al Alam, Denise Frey, Mark R. Trinh, Le A. Fernandez, G. Esteban Warburton, David Fraser, Scott E. Bennett, Daimark Jesudason, Edwin C. SERCA directs cell migration and branching across species and germ layers |
title | SERCA directs cell migration and branching across species and germ layers |
title_full | SERCA directs cell migration and branching across species and germ layers |
title_fullStr | SERCA directs cell migration and branching across species and germ layers |
title_full_unstemmed | SERCA directs cell migration and branching across species and germ layers |
title_short | SERCA directs cell migration and branching across species and germ layers |
title_sort | serca directs cell migration and branching across species and germ layers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665464/ https://www.ncbi.nlm.nih.gov/pubmed/28821490 http://dx.doi.org/10.1242/bio.026039 |
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