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Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions

Inflammatory conditions are critically influenced by neuroimmune crosstalk. Cytokines and neurotrophic factors shape the responses of both nervous and immune systems. Although much progress has been made, most findings to date are based on expression of recombinant (tagged) proteins. The examination...

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Autores principales: Dorschner, Benjamin W., Wiedemuth, Ralf, Funke, Ann-Christin, Gentzel, Marc, Rogers, Mary-Louise, Brenner, Sebastian, Thieme, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085361/
https://www.ncbi.nlm.nih.gov/pubmed/33936068
http://dx.doi.org/10.3389/fimmu.2021.648283
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author Dorschner, Benjamin W.
Wiedemuth, Ralf
Funke, Ann-Christin
Gentzel, Marc
Rogers, Mary-Louise
Brenner, Sebastian
Thieme, Sebastian
author_facet Dorschner, Benjamin W.
Wiedemuth, Ralf
Funke, Ann-Christin
Gentzel, Marc
Rogers, Mary-Louise
Brenner, Sebastian
Thieme, Sebastian
author_sort Dorschner, Benjamin W.
collection PubMed
description Inflammatory conditions are critically influenced by neuroimmune crosstalk. Cytokines and neurotrophic factors shape the responses of both nervous and immune systems. Although much progress has been made, most findings to date are based on expression of recombinant (tagged) proteins. The examination of receptor interactions by immunoprecipitation (IP) at endogenous levels provides further insight into the more subtle regulations of immune responses. Here, we present a comprehensive workflow and an optimized IP protocol that provide step-by-step instructions to investigate neurotrophin receptor p75NTR at endogenous, low abundance levels: from lysate preparation and confirmation of receptor expression to antibody validation and successful detection of protein-protein interactions. We employ human melanoma cell line A375 to validate specific antibodies and IP conditions, and apply these methods to explore p75NTR interactions in human leukemic plasmacytoid dendritic cell line PMDC05 detecting 14-3-3ϵ:p75NTR interaction in this cell type. With p75NTR as an exemplary protein, our approach provides a strategy to detect specific interaction partners even under endogenous, low abundance expression conditions.
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spelling pubmed-80853612021-05-01 Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions Dorschner, Benjamin W. Wiedemuth, Ralf Funke, Ann-Christin Gentzel, Marc Rogers, Mary-Louise Brenner, Sebastian Thieme, Sebastian Front Immunol Immunology Inflammatory conditions are critically influenced by neuroimmune crosstalk. Cytokines and neurotrophic factors shape the responses of both nervous and immune systems. Although much progress has been made, most findings to date are based on expression of recombinant (tagged) proteins. The examination of receptor interactions by immunoprecipitation (IP) at endogenous levels provides further insight into the more subtle regulations of immune responses. Here, we present a comprehensive workflow and an optimized IP protocol that provide step-by-step instructions to investigate neurotrophin receptor p75NTR at endogenous, low abundance levels: from lysate preparation and confirmation of receptor expression to antibody validation and successful detection of protein-protein interactions. We employ human melanoma cell line A375 to validate specific antibodies and IP conditions, and apply these methods to explore p75NTR interactions in human leukemic plasmacytoid dendritic cell line PMDC05 detecting 14-3-3ϵ:p75NTR interaction in this cell type. With p75NTR as an exemplary protein, our approach provides a strategy to detect specific interaction partners even under endogenous, low abundance expression conditions. Frontiers Media S.A. 2021-04-16 /pmc/articles/PMC8085361/ /pubmed/33936068 http://dx.doi.org/10.3389/fimmu.2021.648283 Text en Copyright © 2021 Dorschner, Wiedemuth, Funke, Gentzel, Rogers, Brenner and Thieme https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Dorschner, Benjamin W.
Wiedemuth, Ralf
Funke, Ann-Christin
Gentzel, Marc
Rogers, Mary-Louise
Brenner, Sebastian
Thieme, Sebastian
Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title_full Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title_fullStr Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title_full_unstemmed Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title_short Listening to the Whispers in Neuroimmune Crosstalk: A Comprehensive Workflow to Investigate Neurotrophin Receptor p75NTR Under Endogenous, Low Abundance Conditions
title_sort listening to the whispers in neuroimmune crosstalk: a comprehensive workflow to investigate neurotrophin receptor p75ntr under endogenous, low abundance conditions
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085361/
https://www.ncbi.nlm.nih.gov/pubmed/33936068
http://dx.doi.org/10.3389/fimmu.2021.648283
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