A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair

Author:

Qiu Chen12,Sun Yuan34,Li Jinying12,Zhou Jiayi12,Xu Yuchen5,Qiu Cong12,Yu Kang34,Liu Jia12,Jiang Yuanqing12,Cui Wenyu6,Wang Guanghao7,Liu He12,Yuan Weixin12,Jiang Tuoying12,Kou Yaohui12,Ge Zhen8,He Zhiying910,Zhang Shaomin5,He Yong34ORCID,Yu Luyang12

Affiliation:

1. Key Laboratory of Cardiovascular Intervention and Regenerative Medicine of Zhejiang Province Department of Cardiology Sir Run Run Shaw Hospital Zhejiang University Hangzhou 310058 China

2. MOE Laboratory of Biosystems Homeostasis & Protection and iCell Biotechnology Regenerative Biomedicine Laboratory of College of Life Sciences Zhejiang University Hangzhou 310058 China

3. State Key Laboratory of Fluid Power and Mechatronic Systems School of Mechanical Engineering Zhejiang University Hangzhou 310027 China

4. Key Laboratory of 3D Printing Process and Equipment of Zhejiang Province School of Mechanical Engineering Zhejiang University Hangzhou 310027 China

5. Qiushi Academy for Advanced Studies Zhejiang University Hangzhou 310027 China

6. Eye Center the Second Affiliated Hospital School of Medicine Zhejiang University Hangzhou 310009 China

7. Zhejiang SCI‐TECH University Hangzhou 310018 China

8. School of Pharmaceutical Sciences Hangzhou Medical College Hangzhou 310013 China

9. Institute for Regenerative Medicine Shanghai East Hospital School of Life Sciences and Technology Tongji University Shanghai 200123 China

10. Shanghai Engineering Research Center of Stem Cells Translational Medicine Shanghai 200335 China

Abstract

AbstractStem cells play critical roles in cell therapies and tissue engineering for nerve repair. However, achieving effective delivery of high cell density remains a challenge. Here, a novel cell delivery platform termed the hyper expansion scaffold (HES) is developed to enable high cell loading. HES facilitated self‐promoted and efficient cell absorption via a dual driving force model. In vitro tests revealed that the HES rapidly expanded 80‐fold in size upon absorbing 2.6 million human amniotic epithelial stem cells (hAESCs) within 2 min, representing over a 400% increase in loading capacity versus controls. This enhanced uptake benefited from macroscopic swelling forces as well as microscale capillary action. In spinal cord injury (SCI) rats, HES–hAESCs promoted functional recovery and axonal projection by reducing neuroinflammation and improving the neurotrophic microenvironment surrounding the lesions. In summary, the dual driving forces model provides a new rationale for engineering hydrogel scaffolds to facilitate self‐promoted cell absorption. The HES platform demonstrates great potential as a powerful and efficient vehicle for delivering high densities of hAESCs to promote clinical treatment and repair of SCI.

Funder

Fundamental Research Funds for the Central Universities

China Postdoctoral Science Foundation

National Natural Science Foundation of China

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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