Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Meena, Netra Pal, Kimmel, Alan R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
_version_ 1783244596960034816
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
work_keys_str_mv AT meenanetrapal chemotacticnetworkresponsestolivebacteriashowindependenceofphagocytosisfromchemoreceptorsensing
AT kimmelalanr chemotacticnetworkresponsestolivebacteriashowindependenceofphagocytosisfromchemoreceptorsensing