TY - JOUR
T1 - Normal physiological conditions maintain the biological characteristics of porcine aortic heart valves
T2 - An ex vivo organ culture study
AU - Konduri, Suchitra
AU - Xing, Yun
AU - Warnock, James N.
AU - He, Zhaoming
AU - Yoganathan, Ajit P.
N1 - Funding Information:
This work was supported by the National Science Foundation through the ERC program at the Georgia Institute of Technology under award number EEC-9731643. The authors thank Mr Holifield of Holifield’s farm, Covington, GA, for providing porcine hearts, Tracey Couse for technical assistance in the histological studies and Jennifer Coyne, Stacie Hamel and Jason Xenakis for providing assistance in the study.
PY - 2005/9
Y1 - 2005/9
N2 - The aortic valve functions in a complex mechanical environment which leads to force-dependent cellular and tissue responses. Characterization of these responses provides a fundamental understanding of valve pathogenesis. The aim of this work was to study the biological characteristics of native porcine aortic valves cultured in an ex vivo pulsatile organ culture system capable of maintaining physiological pressures (120/80 mmHg) and cardiac output (4.2 l/min). Collagen, sGAG and elastin contents of the valve leaflets were measured and cusp morphology, cell phenotype, cell proliferation and apoptosis were examined. Presence of endothelial cells (ECs) on the leaflet surface was also evaluated. The differences in collagen, sGAG and elastin contents were not significant (p > 0.05) between the cultured and fresh valve leaflets. The cultured valves maintained the native ECM composition of the leaflets while preserving the morphology and cell phenotype. Cell phenotype in leaflets incubated statically under atmospheric conditions decreased compared to fresh and cultured valve leaflets, indicating the importance of mechanical forces in maintaining the natural biology of the valve leaflets. ECs were retained on the surfaces of cultured leaflets with no remodeling of the leaflets. The number of apoptotic cells in the cultured leaflets was significantly (p < 0.05) less than in the statically incubated leaflets and comparable to fresh leaflets. The sterile ex vivo organ culture system thus maintained the viability and native biological characteristics of the aortic valves that were cultured under dynamic conditions for a period of 48 h.
AB - The aortic valve functions in a complex mechanical environment which leads to force-dependent cellular and tissue responses. Characterization of these responses provides a fundamental understanding of valve pathogenesis. The aim of this work was to study the biological characteristics of native porcine aortic valves cultured in an ex vivo pulsatile organ culture system capable of maintaining physiological pressures (120/80 mmHg) and cardiac output (4.2 l/min). Collagen, sGAG and elastin contents of the valve leaflets were measured and cusp morphology, cell phenotype, cell proliferation and apoptosis were examined. Presence of endothelial cells (ECs) on the leaflet surface was also evaluated. The differences in collagen, sGAG and elastin contents were not significant (p > 0.05) between the cultured and fresh valve leaflets. The cultured valves maintained the native ECM composition of the leaflets while preserving the morphology and cell phenotype. Cell phenotype in leaflets incubated statically under atmospheric conditions decreased compared to fresh and cultured valve leaflets, indicating the importance of mechanical forces in maintaining the natural biology of the valve leaflets. ECs were retained on the surfaces of cultured leaflets with no remodeling of the leaflets. The number of apoptotic cells in the cultured leaflets was significantly (p < 0.05) less than in the statically incubated leaflets and comparable to fresh leaflets. The sterile ex vivo organ culture system thus maintained the viability and native biological characteristics of the aortic valves that were cultured under dynamic conditions for a period of 48 h.
KW - Aortic valve leaflets
KW - Biological properties
KW - Organ culture system
KW - Phenotype
UR - http://www.scopus.com/inward/record.url?scp=24144439141&partnerID=8YFLogxK
U2 - 10.1007/s10439-005-5506-4
DO - 10.1007/s10439-005-5506-4
M3 - Article
C2 - 16133923
AN - SCOPUS:24144439141
SN - 0090-6964
VL - 33
SP - 1158
EP - 1166
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 9
ER -