Related Experiment Video
Updated: Jun 5, 2026

13:05
Micropatterning and Assembly of 3D Microvessels
Published on: September 9, 2016
Perfusable cellulose channels from decellularized leaf scaffolds for modeling vascular amyloidosis
Taeha Lee1, Kang Hyun Lee2, Da Yeon Cheong1
1Department of Biotechnology and Bioinformatics, Korea University, Sejong 30019, South Korea; Interdisciplinary Graduate Program for Artificial Intelligence Smart Convergence Technology, Korea University, Sejong 30019, South Korea.
International Journal of Biological Macromolecules
|March 30, 2025
Summary
Researchers developed a novel decellularized leaf scaffold (DCLS) to model vascular amyloidosis. This scaffold accurately mimics human capillaries, enabling better study of amyloid deposition and clearance in blood vessels.
Area of Science:
- Biomaterials Science
- Vascular Biology
- Biomedical Engineering
Background:
- Amyloid infiltration in blood vessels, or vascular amyloidosis, contributes to tissue damage and disease progression.
- Studying amyloid flow and deposition in capillaries is challenging due to the lack of appropriate in vitro models.
- Existing vascular models do not fully replicate the complex microvasculature of human blood vessels.
Purpose of the Study:
- To develop and validate a novel decellularized leaf scaffold (DCLS) that mimics human capillary structures.
- To utilize the DCLS as a platform for investigating intravascular amyloidosis.
- To assess the efficacy of an amyloid-degrading agent in the DCLS model.
Main Methods:
- Fabrication of a decellularized leaf scaffold (DCLS) preserving cellulose framework and pore structure.
- Validation of DCLS structural integrity and vascular mimicry using fluorescent molecules and colorimetric nanoparticles.
- Perfusion of hen egg-white lysozyme amyloid and subsequent treatment with an amyloid-degrading agent (trypsin).
Main Results:
- The DCLS successfully mimicked complex capillary structures and demonstrated preserved pore structure and responsiveness.
- Amyloid deposition was observed within the DCLS after perfusion with hen egg-white lysozyme.
- Treatment with trypsin resulted in a significant reduction in amyloid deposition (18.3% at 90 min, 25.5% at 180 min).
Conclusions:
- The DCLS provides a realistic and physiologically relevant in vitro model for studying vascular amyloidosis.
- This novel scaffold facilitates research into amyloid accumulation and clearance mechanisms within blood vessels.
- The DCLS platform offers advantages over existing in vitro vascular models for investigating vascular diseases.

