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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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
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
Descripción
Sumario: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.