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Efficient wet-spinning of pre-aligned microtissues for 3D bioprinting complex tissue alignment
Caleb D Vogt1, Joseph R Broomhead2, Kyle Y Kunisaki2
1Medical Scientist Training Program, University of Minnesota-Twin Cities, 420 Delaware Street SE, Minneapolis, MN 55455, United States of America.
Biofabrication
|May 2, 2025
Summary
This study introduces a wet-spinning method to create aligned smooth muscle microtissues for tissue engineering. These pre-aligned microtissues are suitable for 3D bioprinting complex muscle structures.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Precise control of cellular alignment is crucial for engineering functional smooth muscle tissues, especially for complex anatomical sites like the gastroesophageal junction (GEJ).
- Existing methods may lack scalability or require specialized equipment for generating aligned microtissues.
Purpose of the Study:
- To develop a scalable wet-spinning technique for producing pre-aligned microtissues (PAMs) using human esophageal smooth muscle cells.
- To demonstrate the utility of these PAMs in 3D bioprinting applications.
Main Methods:
- Immortalized human esophageal smooth muscle cells were embedded in a collagen-alginate core-shell fiber using a wet-spinning approach.
- Fibers were matured, sectioned into uniform PAMs, and characterized for alignment, cell viability, and contractile marker expression.
- PAMs were integrated into a gelatin-methacryloyl bioink for 3D bioprinting.
Main Results:
- The wet-spinning method successfully generated PAMs with preserved cellular alignment and high cell viability.
- Immunofluorescence and gene expression analyses confirmed the presence of key contractile markers.
- 3D bioprinting demonstrated that PAMs maintain alignment along the extrusion path.
Conclusions:
- The developed wet-spinning approach offers an efficient, scalable, and platform-independent method for producing aligned microtissues.
- This technique shows promise for fabricating anisotropic tissues and reconstructing complex muscle structures like the GEJ.

