Regional and cell specific bioactivity of injectable extracellular matrix biomaterials in myocardial infarction

Myocardial infarction (MI) remains a global health concern. To mitigate subacute and chronic MI pathophysiology, we previously investigated a pro-reparative decellularized extracellular matrix hydrogel. Despite increasing interest in biomaterial scaffolds, single cell and spatially resolved transcriptomics have not been used to probe their therapeutic activity in the heart. Here, we utilize spatial transcriptomics and single nucleus RNA sequencing to delineate the regional and cell-specific bioactivity of extracellular matrix biomaterials. Extracellular matrix hydrogel subacute treatment in female rats induces cardiac resident macrophage preservation, fibroblast activation, and increased lymphatic, vasculature, smooth muscle, and cardiomyocyte development as well as neurogenesis. Chronic treatment in female rats elicits macrophage polarization, neurogenesis, and development of cardiomyocytes, endothelial cells, and fibroblasts. When comparing treatment timepoints, subacute administration has stronger immune modulation, while chronic administration demonstrates higher cardiac development markers. Both subacute and chronic administration are associated with fibroblast activation and vasculature development. Thus, we elucidate undiscovered therapeutic targets of an injectable extracellular matrix hydrogel, further demonstrating the potential of these biomaterials as an MI therapy.

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Publication Details

Journal
Nature Communications
Published
2025-11-24
DOI
https://doi.org/10.1038/s41467-025-65351-5
Citations
1
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
Field-Weighted Citation Impact
2.01

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article

Regional and cell specific bioactivity of injectable extracellular matrix biomaterials in myocardial infarction

Miranda D. Diaz, Karen L. Christman, Zhenxing Fu, David Calcagno et al.
1 citations
Nature Communications
Tissue Engineering and Regenerative Medicine
2.01
article

Regional and cell specific bioactivity of injectable extracellular matrix biomaterials in myocardial infarction

Miranda D. Diaz, Karen L. Christman, Zhenxing Fu, David Calcagno, Michael Nguyen, Jervaughn D. Hunter, Maria Karkanitsa, Kevin R. King, Justin Yu, Nika Taghdiri, Rebecca L. Braden, Joshua M. Mesfin, Van K. Ninh, Alexander Chen, Raymond Wang, J. Pham, C. Luo, Elizabeth Wong, Benjamin D. Bridgelal
article en
1 citations

Abstract

Myocardial infarction (MI) remains a global health concern. To mitigate subacute and chronic MI pathophysiology, we previously investigated a pro-reparative decellularized extracellular matrix hydrogel. Despite increasing interest in biomaterial scaffolds, single cell and spatially resolved transcriptomics have not been used to probe their therapeutic activity in the heart. Here, we utilize spatial transcriptomics and single nucleus RNA sequencing to delineate the regional and cell-specific bioactivity of extracellular matrix biomaterials. Extracellular matrix hydrogel subacute treatment in female rats induces cardiac resident macrophage preservation, fibroblast activation, and increased lymphatic, vasculature, smooth muscle, and cardiomyocyte development as well as neurogenesis. Chronic treatment in female rats elicits macrophage polarization, neurogenesis, and development of cardiomyocytes, endothelial cells, and fibroblasts. When comparing treatment timepoints, subacute administration has stronger immune modulation, while chronic administration demonstrates higher cardiac development markers. Both subacute and chronic administration are associated with fibroblast activation and vasculature development. Thus, we elucidate undiscovered therapeutic targets of an injectable extracellular matrix hydrogel, further demonstrating the potential of these biomaterials as an MI therapy.

Nature CommunicationsVol. 16(1)
UC San Diego Health System (US), University of California San Diego (US), Sanford Consortium for Regenerative Medicine (US), La Jolla Bioengineering Institute (US)
National Science Foundation, American Heart Association, National Institutes of Health, University of California, San Diego, National Heart, Lung, and Blood Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Biomedical Imaging and Bioengineering, School of Medicine, University of California, San Diego
Openalex Percentile: Top 10%
Tissue Engineering and Regenerative Medicine
2.01
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