CCR2 macrophage response determines the functional outcome following cardiomyocyte transplantation.


Journal

Genome medicine
ISSN: 1756-994X
Titre abrégé: Genome Med
Pays: England
ID NLM: 101475844

Informations de publication

Date de publication:
10 08 2023
Historique:
received: 14 03 2023
accepted: 17 07 2023
medline: 14 8 2023
pubmed: 11 8 2023
entrez: 10 8 2023
Statut: epublish

Résumé

The immune response is a crucial factor for mediating the benefit of cardiac cell therapies. Our previous research showed that cardiomyocyte transplantation alters the cardiac immune response and, when combined with short-term pharmacological CCR2 inhibition, resulted in diminished functional benefit. However, the specific role of innate immune cells, especially CCR2 macrophages on the outcome of cardiomyocyte transplantation, is unclear. We compared the cellular, molecular, and functional outcome following cardiomyocyte transplantation in wildtype and T cell- and B cell-deficient Rag2 Compared to wildtype mice, Rag2 Our results demonstrate that the improved functional outcome following cardiomyocyte transplantation is dependent on a specific CCR2 macrophage response. This work highlights the need to study the role of the immune response for cardiomyocyte cell therapy for successful clinical translation.

Sections du résumé

BACKGROUND
The immune response is a crucial factor for mediating the benefit of cardiac cell therapies. Our previous research showed that cardiomyocyte transplantation alters the cardiac immune response and, when combined with short-term pharmacological CCR2 inhibition, resulted in diminished functional benefit. However, the specific role of innate immune cells, especially CCR2 macrophages on the outcome of cardiomyocyte transplantation, is unclear.
METHODS
We compared the cellular, molecular, and functional outcome following cardiomyocyte transplantation in wildtype and T cell- and B cell-deficient Rag2
RESULTS
Compared to wildtype mice, Rag2
CONCLUSIONS
Our results demonstrate that the improved functional outcome following cardiomyocyte transplantation is dependent on a specific CCR2 macrophage response. This work highlights the need to study the role of the immune response for cardiomyocyte cell therapy for successful clinical translation.

Identifiants

pubmed: 37563727
doi: 10.1186/s13073-023-01213-3
pii: 10.1186/s13073-023-01213-3
pmc: PMC10416392
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

61

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Praveen Vasudevan (P)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany.
Rudolf-Zenker-Institute for Experimental Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.

Markus Wolfien (M)

Department of Systems Biology and Bioinformatics, Institute of Computer Science, University of Rostock, 18057, Rostock, Germany.
Institute for Medical Informatics and Biometry, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307, Dresden, Germany.
Center for Scalable Data Analytics and Artificial Intelligence (ScaDS.AI), Dresden/Leipzig, Germany.

Heiko Lemcke (H)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany.

Cajetan Immanuel Lang (CI)

Department of Cardiology, Rostock University Medical Centre, 18057, Rostock, Germany.

Anna Skorska (A)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany.

Ralf Gaebel (R)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany.

Anne-Marie Galow (AM)

Institute of Genome Biology, Research Institute for Farm Animal Biology (FBN), 18196, Dummerstorf, Germany.

Dirk Koczan (D)

Core Facility for Microarray Analysis, Institute for Immunology, Rostock University Medical Centre, 18057, Rostock, Germany.

Tobias Lindner (T)

Core Facility Multimodal Small Animal Imaging, Rostock University Medical Centre, 18057, Rostock, Germany.

Wendy Bergmann (W)

Core Facility for Cell Sorting & Cell Analysis, Laboratory for Clinical Immunology, Rostock University Medical Centre, 18057, Rostock, Germany.

Brigitte Mueller-Hilke (B)

Core Facility for Cell Sorting & Cell Analysis, Laboratory for Clinical Immunology, Rostock University Medical Centre, 18057, Rostock, Germany.

Brigitte Vollmar (B)

Rudolf-Zenker-Institute for Experimental Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.

Bernd Joachim Krause (BJ)

Department of Nuclear Medicine, Rostock University Medical Centre, 18057, Rostock, Germany.

Olaf Wolkenhauer (O)

Rudolf-Zenker-Institute for Experimental Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Stellenbosch Institute of Advanced Study (STIAS), Wallenberg Research Centre at Stellenbosch University, Stellenbosch, 7602, South Africa.

Gustav Steinhoff (G)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany.

Robert David (R)

Department of Cardiac Surgery, Rostock University Medical Centre, 18057, Rostock, Germany. Robert.David@med.uni-rostock.de.
Department of Life, Light and Matter, University of Rostock, Albert-Einstein-Str. 25, 18059, Rostock, Germany. Robert.David@med.uni-rostock.de.

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