TY - JOUR
T1 - Decellularization of human iliac artery
T2 - A vascular scaffold for peripheral repairs with human mesenchymal cells
AU - Abad-Contreras, David E.
AU - Martínez-Ortiz, Ana K.
AU - Martínez-López, Valentín
AU - Laparra-Escareño, Hugo
AU - Martínez-García, Francisco Drusso
AU - Pérez-Calixto, Daniel
AU - Vazquez-Victorio, Genaro
AU - Sepúlveda-Robles, Omar
AU - Rosas-Vargas, Haydeé
AU - Piña-Barba, Cristina
AU - Rodríguez-López, Leonardo A.
AU - Giraldo-Gomez, David M.
AU - Hinojosa, Carlos A.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2025/4
Y1 - 2025/4
N2 - This work presents strong evidence supporting the use of decellularized human iliac arteries combined with adipose tissue-derived stem cells (hASCs) as a promising alternative for vascular tissue engineering, opening the path to future treatments for peripheral artery disease (PAD). PAD is a progressive condition with high rates of amputation and mortality due to ischemic damage and limited graft options. Traditional synthetic grafts often fail due to poor integration, while autologous grafts may be unsuitable for patients with compromised vascular health. This study explores the potential of decellularized human iliac arteries as scaffolds for vascular grafts, focusing on preserving extracellular matrix (ECM) ultrastructure while minimizing immunogenic response. A perfusion-based protocol with enzymatic and detergent agents effectively removed cellular material, resulting in scaffolds with preserved ECM architecture, including organized collagen and elastin fibers. To assess scaffold bioactivity, hASCs were seeded onto the decellularized ECM, demonstrating high viability. Structural assessments, including histological staining and mechanical testing, confirmed that decellularized arteries retained their hierarchical structure and exhibited increased stiffness, suggesting an adaptive realignment of ECM fibers. Thermal and ultrastructural analyses further showed that decellularized scaffolds maintained stability and integrity comparable to native tissue, underscoring their durability for clinical applications. The human iliac artery shows potential as a vascular scaffold due to its accessibility and the ability to support the viability of hASC. Future research will emphasize in vivo validation and strategies for functional recellularization to evaluate the clinical viability of these engineered vascular grafts.
AB - This work presents strong evidence supporting the use of decellularized human iliac arteries combined with adipose tissue-derived stem cells (hASCs) as a promising alternative for vascular tissue engineering, opening the path to future treatments for peripheral artery disease (PAD). PAD is a progressive condition with high rates of amputation and mortality due to ischemic damage and limited graft options. Traditional synthetic grafts often fail due to poor integration, while autologous grafts may be unsuitable for patients with compromised vascular health. This study explores the potential of decellularized human iliac arteries as scaffolds for vascular grafts, focusing on preserving extracellular matrix (ECM) ultrastructure while minimizing immunogenic response. A perfusion-based protocol with enzymatic and detergent agents effectively removed cellular material, resulting in scaffolds with preserved ECM architecture, including organized collagen and elastin fibers. To assess scaffold bioactivity, hASCs were seeded onto the decellularized ECM, demonstrating high viability. Structural assessments, including histological staining and mechanical testing, confirmed that decellularized arteries retained their hierarchical structure and exhibited increased stiffness, suggesting an adaptive realignment of ECM fibers. Thermal and ultrastructural analyses further showed that decellularized scaffolds maintained stability and integrity comparable to native tissue, underscoring their durability for clinical applications. The human iliac artery shows potential as a vascular scaffold due to its accessibility and the ability to support the viability of hASC. Future research will emphasize in vivo validation and strategies for functional recellularization to evaluate the clinical viability of these engineered vascular grafts.
KW - Arteries
KW - Biomimetic materials
KW - Decellularization
KW - Extracellular matrix (ECM)
KW - Mesenchymal stem cells
KW - Regenerative medicine
KW - Tissue engineering
KW - Vascular graft
UR - http://www.scopus.com/inward/record.url?scp=85213023673&partnerID=8YFLogxK
U2 - 10.1016/j.tice.2024.102686
DO - 10.1016/j.tice.2024.102686
M3 - Article
C2 - 39724840
AN - SCOPUS:85213023673
SN - 0040-8166
VL - 93
JO - Tissue and Cell
JF - Tissue and Cell
M1 - 102686
ER -