TY - JOUR
T1 - Tissue-Engineered Neo-Urinary Conduit from Decellularized Trachea
AU - Singh, Anirudha
AU - Lee, David
AU - Jeong, Harrison
AU - Yu, Christine
AU - Li, Jiuru
AU - Fang, Chen Hao
AU - Sabnekar, Praveena
AU - Liu, Xiaopu
AU - Yoshida, Takahiro
AU - Sopko, Nikolai
AU - Bivalacqua, Trinity J.
N1 - Funding Information:
Funding sources gratefully acknowledged are the Johns Hopkins Greenberg Bladder Cancer Award and Johns Hopkins Brady Urological Institute start up funding. The authors also thank Dr. Brian Crawford of the Department of Materials Science and Engineering of Johns Hopkins University for allowing us to perform experiments on Instron tensile testing equipment.
Funding Information:
Sources gratefully acknowledged are the Johns Hopkins Greenberg Bladder Cancer Award and Johns Hopkins Brady Urological Institute start up funding. The authors also thank Dr. Brian Crawford of the Department of Materials Science and Engineering of Johns Hopkins University for allowing us to perform experiments on Instron tensile testing equipment.
Publisher Copyright:
© Copyright 2018, Mary Ann Liebert, Inc.
PY - 2018/10
Y1 - 2018/10
N2 - Decellularized tissues have been increasingly popular for constructing scaffolds for tissue engineering applications due to their beneficial biological compositions and mechanical properties. It is therefore natural to consider decellularized trachea for construction of tissue-engineered trachea, as well as other tubular organs. A Neo-Urinary Conduit (NUC) is such a tubular organ that works as a passage for urine removal in bladder cancer patients who need a urinary diversion after their diseased bladder is removed. In this study, we report our findings on the feasibility of using a decellularized trachea for NUC applications. As a NUC scaffold, decellularized trachea provides benefits of having not only naturally occurring biological components but also having sufficient mechanical properties and structural integrity. We, therefore, decellularized rabbit trachea, evaluated its mechanical performance, and investigated its ability to support in vitro growth of human smooth muscle cells (hSMCs) and human urothelial cells (hUCs). The decellularized trachea had appropriate biomechanical properties with ultimate tensile strength of ∼0.34 MPa in longitudinal direction and ∼1.0 MPa in circumferential direction and resisted a radial burst pressure of >155 mm Hg. Cell morphology study by scanning electron microscopy further showed that hUCs grown on decellularized trachea adopted a typical flatten and interconnected network structure in the lumen of the scaffold, while they formed a round spherical shape and did not spread on the outer surfaces. SMCs, on the other hand, spread well throughout the scaffold. The gene expression analysis by real time quantitative polymerase chain reaction (RT-qPCR) and immunofluorescence studies further confirmed scaffold's ability to support long-term growth of hSMCs. Since uroepithelium has been shown to regenerate itself over time in vivo, these findings suggest that it is possible to construct a NUC from decellularized trachea without any preseeding of UCs. In future, we plan to translate decellularized trachea in a preclinical animal model and evaluate its biological performance.
AB - Decellularized tissues have been increasingly popular for constructing scaffolds for tissue engineering applications due to their beneficial biological compositions and mechanical properties. It is therefore natural to consider decellularized trachea for construction of tissue-engineered trachea, as well as other tubular organs. A Neo-Urinary Conduit (NUC) is such a tubular organ that works as a passage for urine removal in bladder cancer patients who need a urinary diversion after their diseased bladder is removed. In this study, we report our findings on the feasibility of using a decellularized trachea for NUC applications. As a NUC scaffold, decellularized trachea provides benefits of having not only naturally occurring biological components but also having sufficient mechanical properties and structural integrity. We, therefore, decellularized rabbit trachea, evaluated its mechanical performance, and investigated its ability to support in vitro growth of human smooth muscle cells (hSMCs) and human urothelial cells (hUCs). The decellularized trachea had appropriate biomechanical properties with ultimate tensile strength of ∼0.34 MPa in longitudinal direction and ∼1.0 MPa in circumferential direction and resisted a radial burst pressure of >155 mm Hg. Cell morphology study by scanning electron microscopy further showed that hUCs grown on decellularized trachea adopted a typical flatten and interconnected network structure in the lumen of the scaffold, while they formed a round spherical shape and did not spread on the outer surfaces. SMCs, on the other hand, spread well throughout the scaffold. The gene expression analysis by real time quantitative polymerase chain reaction (RT-qPCR) and immunofluorescence studies further confirmed scaffold's ability to support long-term growth of hSMCs. Since uroepithelium has been shown to regenerate itself over time in vivo, these findings suggest that it is possible to construct a NUC from decellularized trachea without any preseeding of UCs. In future, we plan to translate decellularized trachea in a preclinical animal model and evaluate its biological performance.
KW - bladder cancer
KW - decellularized tissues
KW - neo-urinary conduit
KW - scaffolds
KW - trachea
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UR - http://www.scopus.com/inward/citedby.url?scp=85054435327&partnerID=8YFLogxK
U2 - 10.1089/ten.tea.2017.0436
DO - 10.1089/ten.tea.2017.0436
M3 - Article
C2 - 29649957
AN - SCOPUS:85054435327
VL - 24
SP - 1456
EP - 1467
JO - Tissue Engineering - Part A.
JF - Tissue Engineering - Part A.
SN - 1937-3341
IS - 19-20
ER -