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Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing
Aspects of innate immunity derive from characteristics inherent to phagocytes, including chemotaxis toward and engulfment of unicellular organisms or cell debris. Ligand chemotaxis has been biochemically investigated using mammalian and model systems, but precision of chemotaxis towards ligands bein...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476428/ https://www.ncbi.nlm.nih.gov/pubmed/28541182 http://dx.doi.org/10.7554/eLife.24627 |
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author | Meena, Netra Pal Kimmel, Alan R |
author_facet | Meena, Netra Pal Kimmel, Alan R |
author_sort | Meena, Netra Pal |
collection | PubMed |
description | Aspects of innate immunity derive from characteristics inherent to phagocytes, including chemotaxis toward and engulfment of unicellular organisms or cell debris. Ligand chemotaxis has been biochemically investigated using mammalian and model systems, but precision of chemotaxis towards ligands being actively secreted by live bacteria is not well studied, nor has there been systematic analyses of interrelationships between chemotaxis and phagocytosis. The genetic/molecular model Dictyostelium and mammalian phagocytes share mechanistic pathways for chemotaxis and phagocytosis; Dictyostelium chemotax toward bacteria and phagocytose them as food sources. We quantified Dictyostelium chemotaxis towards live gram positive and gram negative bacteria and demonstrate high sensitivity to multiple bacterially-secreted chemoattractants. Additive/competitive assays indicate that intracellular signaling-networks for multiple ligands utilize independent upstream adaptive mechanisms, but common downstream targets, thus amplifying detection at low signal propagation, but strengthening discrimination of multiple inputs. Finally, analyses of signaling-networks for chemotaxis and phagocytosis indicate that chemoattractant receptor-signaling is not essential for bacterial phagocytosis. DOI: http://dx.doi.org/10.7554/eLife.24627.001 |
format | Online Article Text |
id | pubmed-5476428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54764282017-06-21 Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing Meena, Netra Pal Kimmel, Alan R eLife Cell Biology Aspects of innate immunity derive from characteristics inherent to phagocytes, including chemotaxis toward and engulfment of unicellular organisms or cell debris. Ligand chemotaxis has been biochemically investigated using mammalian and model systems, but precision of chemotaxis towards ligands being actively secreted by live bacteria is not well studied, nor has there been systematic analyses of interrelationships between chemotaxis and phagocytosis. The genetic/molecular model Dictyostelium and mammalian phagocytes share mechanistic pathways for chemotaxis and phagocytosis; Dictyostelium chemotax toward bacteria and phagocytose them as food sources. We quantified Dictyostelium chemotaxis towards live gram positive and gram negative bacteria and demonstrate high sensitivity to multiple bacterially-secreted chemoattractants. Additive/competitive assays indicate that intracellular signaling-networks for multiple ligands utilize independent upstream adaptive mechanisms, but common downstream targets, thus amplifying detection at low signal propagation, but strengthening discrimination of multiple inputs. Finally, analyses of signaling-networks for chemotaxis and phagocytosis indicate that chemoattractant receptor-signaling is not essential for bacterial phagocytosis. DOI: http://dx.doi.org/10.7554/eLife.24627.001 eLife Sciences Publications, Ltd 2017-05-25 /pmc/articles/PMC5476428/ /pubmed/28541182 http://dx.doi.org/10.7554/eLife.24627 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cell Biology Meena, Netra Pal Kimmel, Alan R Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title | Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title_full | Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title_fullStr | Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title_full_unstemmed | Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title_short | Chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
title_sort | chemotactic network responses to live bacteria show independence of phagocytosis from chemoreceptor sensing |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476428/ https://www.ncbi.nlm.nih.gov/pubmed/28541182 http://dx.doi.org/10.7554/eLife.24627 |
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