A Novel Conductive Polypyrrole‐Chitosan Hydrogel Containing Human Endometrial Mesenchymal Stem Cell‐Derived Exosomes Facilitated Sustained Release for Cardiac Repair

Author:

Yan Changping12ORCID,Wang Xinzhu1,Wang Qi1,Li Haiyan1,Song Huifang13,Zhou Jingli4,Peng Zexu1,Yin Wenjuan1,Fan Xuemei1,Yang Kun1,Zhou Bingrui1,Liang Yuxiang1,Jiang Zengyu1,Shi Yuwei15,Zhang Sanyuan1,He Sheng1ORCID,Li Ren‐Ke6ORCID,Xie Jun1

Affiliation:

1. The First Hospital of Shanxi Medical University Department of Biochemistry and Molecular Biology Shanxi Key Laboratory of Birth Defect and Cell Regeneration MOE Key Laboratory of Coal Environmental Pathogenicity and Prevention Shanxi Medical University Taiyuan 030001 China

2. Department of Gynecology Affiliated Cancer Hospital of Shanxi Medical University Taiyuan 030013 China

3. Department of Anatomy Shanxi Medical University Taiyuan 030001 China

4. Shanxi Provincial People's Hospital Affiliated Hospital of Shanxi Medical University Taiyuan 030012 China

5. NHC Key Laboratory of Pneumoconiosis Shanxi Province Key Laboratory of Respiratory Department of Pulmonary and Critical Care Medicine The First Hospital of Shanxi Medical University Taiyuan 030001 China

6. Toronto General Hospital Research Institute Division of Cardiovascular Surgery University Health Network University of Toronto Toronto ON M5G 2C4 Canada

Abstract

AbstractMyocardial infarction (MI) results in cardiomyocyte necrosis and conductive system damage, leading to sudden cardiac death and heart failure. Studies have shown that conductive biomaterials can restore cardiac conduction, but cannot facilitate tissue regeneration. This study aims to add regenerative capabilities to the conductive biomaterial by incorporating human endometrial mesenchymal stem cell (hEMSC)‐derived exosomes (hEMSC‐Exo) into poly‐pyrrole‐chitosan (PPY‐CHI), to yield an injectable hydrogel that can effectively treat MI. In vitro, PPY‐CHI/hEMSC‐Exo, compared to untreated controls, PPY‐CHI, or hEMSC‐Exo alone, alleviates H2O2‐induced apoptosis and promotes tubule formation, while in vivo, PPY‐CHI/hEMSC‐Exo improves post‐MI cardiac functioning, along with counteracting against ventricular remodeling and fibrosis. All these activities are facilitated via increased epidermal growth factor (EGF)/phosphoinositide 3‐kinase (PI3K)/AKT signaling. Furthermore, the conductive properties of PPY‐CHI/hEMSC‐Exo are able to resynchronize cardiac electrical transmission to alleviate arrythmia. Overall, PPY‐CHI/hEMSC‐Exo synergistically combines the cardiac regenerative capabilities of hEMSC‐Exo with the conductive properties of PPY‐CHI to improve cardiac functioning, via promoting angiogenesis and inhibiting apoptosis, as well as resynchronizing electrical conduction, to ultimately enable more effective MI treatment. Therefore, incorporating exosomes into a conductive hydrogel provides dual benefits in terms of maintaining conductivity, along with facilitating long‐term exosome release and sustained application of their beneficial effects.

Funder

National Natural Science Foundation of China

Postdoctoral Research Foundation of China

Shanxi Scholarship Council of China

Canadian Institutes of Health Research

Heart and Stroke Foundation of Canada

Publisher

Wiley

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