Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro

Abstract Background The immunomodulatory function of human mesenchymal stromal cells (MSCs) strongly depends on external factors; such as cytokines and other signalling molecules encountered in the disease microenvironment. An insufficiently inflammatory environment can fail to activate MSCs, and ce...

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Main Authors: Courteney Tunstead, Laura M. Bitterlich, James A. Ankrum, Andrew E. Hogan, Karen English
Format: Article
Language:English
Published: BMC 2025-08-01
Series:Stem Cell Research & Therapy
Online Access:https://doi.org/10.1186/s13287-025-04536-7
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author Courteney Tunstead
Laura M. Bitterlich
James A. Ankrum
Andrew E. Hogan
Karen English
author_facet Courteney Tunstead
Laura M. Bitterlich
James A. Ankrum
Andrew E. Hogan
Karen English
author_sort Courteney Tunstead
collection DOAJ
description Abstract Background The immunomodulatory function of human mesenchymal stromal cells (MSCs) strongly depends on external factors; such as cytokines and other signalling molecules encountered in the disease microenvironment. An insufficiently inflammatory environment can fail to activate MSCs, and certain signals can impair their function. Obesity is on the rise worldwide, making it an additional factor to be considered prior to MSC therapy, as the microenvironment presents its own challenges. Elevated levels of serum free fatty acids, specifically palmitate, have the potential to affect MSC therapy. Palmitate-exposure has been shown to impair MSC immunomodulation of T cells in vitro. However, this is yet to be studied in the context of macrophages. Methods MSCs from three independent donors were exposed to 0.4mM of palmitate for 6–24 h. Gene expression, protein production and functional capacity were then assessed in response to palmitate. A ceramide synthesis inhibitor (Fumonisin B1) and a CC-chemokine ligand 2 (CCL2)-neutralising antibody were further used to assess the impact of these components on palmitate-associated immunomodulation. Results We demonstrated that palmitate-exposed MSCs have enhanced suppression of human monocyte-derived macrophage (MDM) production of tumour necrosis factor α (TNFα), in a CCL2-dependent manner. We further elucidated parts of the pathway, such as ceramide synthesis, through which palmitate promotes this enhanced immunomodulation of macrophages. Conclusion Palmitate-exposed MSCs show enhanced immunomodulation of human MDMs, through the ceramide/CCL2 axis in vitro.
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spelling doaj-art-b387b0e8cc1b474cb0ddf0fad7aec7f92025-08-20T03:42:40ZengBMCStem Cell Research & Therapy1757-65122025-08-0116111510.1186/s13287-025-04536-7Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitroCourteney Tunstead0Laura M. Bitterlich1James A. Ankrum2Andrew E. Hogan3Karen English4Kathleen Lonsdale Institute for Human Health Research, Maynooth UniversityKathleen Lonsdale Institute for Human Health Research, Maynooth UniversityUniversity of Iowa Fraternal Order of Eagles Diabetes Research Center, University of IowaKathleen Lonsdale Institute for Human Health Research, Maynooth UniversityKathleen Lonsdale Institute for Human Health Research, Maynooth UniversityAbstract Background The immunomodulatory function of human mesenchymal stromal cells (MSCs) strongly depends on external factors; such as cytokines and other signalling molecules encountered in the disease microenvironment. An insufficiently inflammatory environment can fail to activate MSCs, and certain signals can impair their function. Obesity is on the rise worldwide, making it an additional factor to be considered prior to MSC therapy, as the microenvironment presents its own challenges. Elevated levels of serum free fatty acids, specifically palmitate, have the potential to affect MSC therapy. Palmitate-exposure has been shown to impair MSC immunomodulation of T cells in vitro. However, this is yet to be studied in the context of macrophages. Methods MSCs from three independent donors were exposed to 0.4mM of palmitate for 6–24 h. Gene expression, protein production and functional capacity were then assessed in response to palmitate. A ceramide synthesis inhibitor (Fumonisin B1) and a CC-chemokine ligand 2 (CCL2)-neutralising antibody were further used to assess the impact of these components on palmitate-associated immunomodulation. Results We demonstrated that palmitate-exposed MSCs have enhanced suppression of human monocyte-derived macrophage (MDM) production of tumour necrosis factor α (TNFα), in a CCL2-dependent manner. We further elucidated parts of the pathway, such as ceramide synthesis, through which palmitate promotes this enhanced immunomodulation of macrophages. Conclusion Palmitate-exposed MSCs show enhanced immunomodulation of human MDMs, through the ceramide/CCL2 axis in vitro.https://doi.org/10.1186/s13287-025-04536-7
spellingShingle Courteney Tunstead
Laura M. Bitterlich
James A. Ankrum
Andrew E. Hogan
Karen English
Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
Stem Cell Research & Therapy
title Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
title_full Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
title_fullStr Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
title_full_unstemmed Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
title_short Palmitate enhances MSC immunomodulation of human macrophages via the ceramide/CCL2 axis in vitro
title_sort palmitate enhances msc immunomodulation of human macrophages via the ceramide ccl2 axis in vitro
url https://doi.org/10.1186/s13287-025-04536-7
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