|
|
||||||||
J Thorac Cardiovasc Surg 2000;120:596-603
© 2000 The American Association for Thoracic Surgery
Surgery for Congenital Heart Disease |
From the Division of Cardiovascular Surgery, Department of Surgery, Children's Hospital and Regional Medical Center, and the University of Washington, Seattle, Wash.
Address for reprints: Flavian M. Lupinetti, MD, Children's Hospital and Medical Center, 4800 Sand Point Way, NE, Seattle, WA 98105 (E-mail: mlupin{at}chmc.org ).
Objective: Allograft valves are frequently used in the repair of congenital cardiac anomalies. The failure rate may differ depending on the type of allograft used. Previous studies have shown that rat aortic valve grafts exhibit synthesis of procollagen, suggesting a capacity for repair and regeneration after implantation. No studies of pulmonary valve grafts in the heterotopic rat implant model have thus far been reported. This study was designed to investigate whether pulmonary valve grafts maintain in vivo viability, as demonstrated by procollagen synthesis, and whether cryopreservation, histocompatibility, or both affect this property.
Methods: Cryopreserved and fresh rat pulmonary valves were implanted into the abdominal aorta of syngeneic and allogeneic recipients. The grafts and native valves were excised 3 to 21 days after implantation. Valves were sectioned and immunohistochemically stained for procollagen. Computerized morphometry was used to calculate changes in intima, media, and adventitia as a percentage of cross-sectional area of the graft. Procollagen content was graded by semiquantitative methods.
Results: Pulmonary valve grafts had significantly greater collagen density in the intima and adventitia compared with native aortic and pulmonary tissues, but collagen density in the media was similar in all groups. The grafts demonstrated appreciably greater procollagen than the corresponding native valves. These findings were consistent in all grafts (ie, both fresh and cryopreserved, both syngeneic and allogeneic), irrespective of duration of implantation.
Conclusions: Procollagen synthesis occurs in pulmonary valve grafts early after implantation, indicating viability of these tissues. This model of pulmonary valve implantation may have wide applicability to questions of allograft biology.
This article has been cited by other articles:
![]() |
K. Schenke-Layland, N. Madershahian, I. Riemann, B. Starcher, K.-J. Halbhuber, K. Konig, and U. A. Stock Impact of Cryopreservation on Extracellular Matrix Structures of Heart Valve Leaflets. Ann. Thorac. Surg., March 1, 2006; 81(3): 918 - 926. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Leask Invited commentary. Ann. Thorac. Surg., March 1, 2006; 81(3): 927 - 927. [Full Text] [PDF] |
||||
![]() |
R. E. Shaddy and J. A. Hawkins Immunology and failure of valved allografts in children Ann. Thorac. Surg., October 1, 2002; 74(4): 1271 - 1275. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |