Bilayered vascular graft derived from human induced pluripotent stem cells with biomimetic structure and function

Author:

Nakayama Karina H123,Joshi Prajakta A34,Lai Edwina S5,Gujar Prachi6,Joubert Lydia-M7,Chen Bertha6,Huang Ngan F123

Affiliation:

1. Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305, USA

2. Department of Cardiothoracic Surgery, Stanford University, 300 Pasteur Drive, Stanford, CA 94305-5407, USA

3. Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304, USA

4. Department of Biological Sciences, San Jose State University, San Jose, CA 95112, USA

5. Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA

6. Department of Obstetrics & Gynecology, Stanford University, Stanford, CA 94305, USA

7. Cell Sciences Imaging Facility, Stanford University, Stanford, CA 94305, USA

Abstract

Background: We developed an aligned bi-layered vascular graft derived from human induced pluripotent stem cells (iPSCs) that recapitulates the cellular composition, orientation, and anti-inflammatory function of blood vessels. Materials & methods: The luminal layer consisted of longitudinal-aligned nanofibrillar collagen containing primary endothelial cells (ECs) or iPSC-derived ECs (iPSC-ECs). The outer layer contained circumferentially oriented nanofibrillar collagen with primary smooth muscle cells (SMCs) or iPSC-derived SMCs(iPSC-SMCs). Results: On the aligned scaffolds, cells organized F-actin assembly within 8º from the direction of nanofibrils. When compared to randomly-oriented scaffolds, EC-seeded aligned scaffolds had significant reduced inflammatory response, based on adhesivity to monocytes. Conclusion: This study highlights the importance of anisotropic scaffolds in directing cell form and function, and has therapeutic significance as physiologically relevant blood vessels.

Publisher

Future Medicine Ltd

Subject

Embryology,Biomedical Engineering

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