Peripheral blood mesenchymal stem cell‐derived exosomes improve renal sympathetic denervation efficacy through β‐catenin‐mediated cardiac reprogramming

Myocardial infarction triggers cardiomyocyte depletion and sympathetic overactivation, culminating in irreversible heart failure. Renal denervation (RD) attenuates sympathetic signalling, modulating catecholamine‒B-type natriuretic peptide (BNP) homeostasis. We newly demonstrate RD-enhanced peripheral blood mesenchymal stem cell exosomal secretion enriched with miR-141-200-429 clusters. These exosomal miRNAs suppress dickkopf-1 (Dkk1), activating GSK3β/Wnt/β-catenin signalling to enhance myocardial survival and regeneration. Our findings establish a combined therapeutic paradigm wherein RD maintains durable efficacy and safety alongside complementary interventions for heart failure management.

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Publication Details

Journal
Clinical and Translational Medicine
Published
2025-09-01
DOI
https://doi.org/10.1002/ctm2.70475
Citations
2
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
Field-Weighted Citation Impact
4.01

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article

Peripheral blood mesenchymal stem cell‐derived exosomes improve renal sympathetic denervation efficacy through β‐catenin‐mediated cardiac reprogramming

Pengzhen Wang, Jianshuo Wang, Lan Zhao, Zhanyu Deng et al.
2 citations
Clinical and Translational Medicine
Tissue Engineering and Regenerative Medicine
4.01
article

Peripheral blood mesenchymal stem cell‐derived exosomes improve renal sympathetic denervation efficacy through β‐catenin‐mediated cardiac reprogramming

Pengzhen Wang, Jianshuo Wang, Lan Zhao, Zhanyu Deng, Shaoheng Zhang, Yanwen Deng, Li Chen, Zhichuan Huang
article en
2 citations

Abstract

Myocardial infarction triggers cardiomyocyte depletion and sympathetic overactivation, culminating in irreversible heart failure. Renal denervation (RD) attenuates sympathetic signalling, modulating catecholamine‒B-type natriuretic peptide (BNP) homeostasis. We newly demonstrate RD-enhanced peripheral blood mesenchymal stem cell exosomal secretion enriched with miR-141-200-429 clusters. These exosomal miRNAs suppress dickkopf-1 (Dkk1), activating GSK3β/Wnt/β-catenin signalling to enhance myocardial survival and regeneration. Our findings establish a combined therapeutic paradigm wherein RD maintains durable efficacy and safety alongside complementary interventions for heart failure management.

Clinical and Translational MedicineVol. 15(9)
Jinan University (CN), Nanfang Hospital (CN), Dahua Hospital (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 6%
Tissue Engineering and Regenerative Medicine
4.01
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