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Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages

(1) The monocytic leukemia cell line THP-1 and primary monocyte-derived macrophages (MDMs) are popular in vitro model systems to study human innate immunity, wound healing, and tissue regeneration. However, both cell types differ significantly in their origin and response to activation stimuli. (2)...

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Autores principales: Feuerer, Nora, Carvajal Berrio, Daniel A., Billing, Florian, Segan, Sören, Weiss, Martin, Rothbauer, Ulrich, Marzi, Julia, Schenke-Layland, Katja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139061/
https://www.ncbi.nlm.nih.gov/pubmed/35625726
http://dx.doi.org/10.3390/biomedicines10050989
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author Feuerer, Nora
Carvajal Berrio, Daniel A.
Billing, Florian
Segan, Sören
Weiss, Martin
Rothbauer, Ulrich
Marzi, Julia
Schenke-Layland, Katja
author_facet Feuerer, Nora
Carvajal Berrio, Daniel A.
Billing, Florian
Segan, Sören
Weiss, Martin
Rothbauer, Ulrich
Marzi, Julia
Schenke-Layland, Katja
author_sort Feuerer, Nora
collection PubMed
description (1) The monocytic leukemia cell line THP-1 and primary monocyte-derived macrophages (MDMs) are popular in vitro model systems to study human innate immunity, wound healing, and tissue regeneration. However, both cell types differ significantly in their origin and response to activation stimuli. (2) Resting THP-1 and MDMs were stimulated with lipopolysaccharide (LPS) and interferon γ (IFNγ) and analyzed by Raman microspectroscopy (RM) before and 48 h after activation. Raman data were subsequently analyzed using principal component analysis. (3) We were able to resolve and analyze the spatial distribution and molecular composition of proteins, nucleic acids, and lipids in resting and activated THP-1 and MDMs. Our findings reveal that proinflammatory activation-induced significant spectral alterations at protein and phospholipid levels in THP-1. In MDMs, we identified that nucleic acid and non-membrane-associated intracellular lipid composition were also affected. (4) Our results show that it is crucial to carefully choose the right cell type for an in vitro model as the nature of the cells itself may impact immune cell polarization or activation results. Moreover, we demonstrated that RM is a sensitive tool for investigating cell-specific responses to activation stimuli and monitoring molecular changes in subcellular structures.
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spelling pubmed-91390612022-05-28 Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages Feuerer, Nora Carvajal Berrio, Daniel A. Billing, Florian Segan, Sören Weiss, Martin Rothbauer, Ulrich Marzi, Julia Schenke-Layland, Katja Biomedicines Article (1) The monocytic leukemia cell line THP-1 and primary monocyte-derived macrophages (MDMs) are popular in vitro model systems to study human innate immunity, wound healing, and tissue regeneration. However, both cell types differ significantly in their origin and response to activation stimuli. (2) Resting THP-1 and MDMs were stimulated with lipopolysaccharide (LPS) and interferon γ (IFNγ) and analyzed by Raman microspectroscopy (RM) before and 48 h after activation. Raman data were subsequently analyzed using principal component analysis. (3) We were able to resolve and analyze the spatial distribution and molecular composition of proteins, nucleic acids, and lipids in resting and activated THP-1 and MDMs. Our findings reveal that proinflammatory activation-induced significant spectral alterations at protein and phospholipid levels in THP-1. In MDMs, we identified that nucleic acid and non-membrane-associated intracellular lipid composition were also affected. (4) Our results show that it is crucial to carefully choose the right cell type for an in vitro model as the nature of the cells itself may impact immune cell polarization or activation results. Moreover, we demonstrated that RM is a sensitive tool for investigating cell-specific responses to activation stimuli and monitoring molecular changes in subcellular structures. MDPI 2022-04-25 /pmc/articles/PMC9139061/ /pubmed/35625726 http://dx.doi.org/10.3390/biomedicines10050989 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Feuerer, Nora
Carvajal Berrio, Daniel A.
Billing, Florian
Segan, Sören
Weiss, Martin
Rothbauer, Ulrich
Marzi, Julia
Schenke-Layland, Katja
Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title_full Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title_fullStr Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title_full_unstemmed Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title_short Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages
title_sort raman microspectroscopy identifies biochemical activation fingerprints in thp-1- and pbmc-derived macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139061/
https://www.ncbi.nlm.nih.gov/pubmed/35625726
http://dx.doi.org/10.3390/biomedicines10050989
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