Comparative assessment of intimal hyperplasia development after 14 days in two different experimental settings: Tissue culture versus ex vivo continuous perfusion of human saphenous vein

• Published in: The Journal of surgical research 2004-09, Vol.121 (1), p.42-49
• Main Authors: Rey, J., Probst, H., Mazzolai, L., Bosman, F.T.B., Pusztaszeri, M., Stergiopulos, N., Ris, H.B., Hayoz, D., Saucy, F., Corpataux, J.M.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Culture Techniques; ex vivo perfusion; Female; fibrinolytic factor; flow; General aspects; histomorphometry; Humans; Hyperplasia; immunohistochemistry; intimal hyperplasia; Male; Medical sciences; PAI-1; Perfusion; saphenous vein; Saphenous Vein - pathology; Time Factors; Tunica Intima - pathology; vein culture
• ISSN: 0022-4804; 1095-8673
• DOI: 10.1016/j.jss.2004.04.003

Intimal hyperplasia (IH) is a vascular remodeling process which often leads to failure of arterial bypass or hemodialysis access. Experimental and clinical work have provided insight in IH development; however, further studies under precise controlled conditions are required to improve therapeutic strategies to inhibit IH development. Ex vivo perfusion of human vessel segments under standardized hemodynamic conditions may provide an adequate experimental approach for this purpose. Therefore, chronically perfused venous segments were studied and compared to traditional static culture procedures with regard to functional and histomorphologic characteristics as well as gene expression. Static vein culture allowing high tissue viability was performed as previously described. Ex vivo vein support system (EVVSS) was performed using a vein support system consisting of an incubator with a perfusion chamber and a pump. EVVSS allows vessel perfusion under continuous flow while maintaining controlled hemodynamic conditions. Each human saphenous vein was divided in two parts, one cultured in a Pyrex dish and the other part perfused in EVVSS for 14 days. Testing of vasomotion, histomorphometry, expression of CD 31, Factor VIII, MIB 1, α-actin, and PAI-l were determined before and after 14 days of either experimental conditions. Human venous segments cultured under traditional or perfused conditions exhibited similar IH after 14 days as shown by histomorphometry. Smooth-muscle cell (SMC) was preserved after chronic perfusion. Although integrity of both endothelial and smooth-muscle cells appears to be maintained in both culture conditions as confirmed by CD31, factor VIII, and α-actin expression, a few smooth-muscle cells in the media stained positive for factor VIII. Cell-proliferation marker MIB-1 was also detected in the two settings and PAI-1 mRNA expression and activity increased significantly after 14 days of culture and perfusion. This study demonstrates the feasibility to chronically perfuse human vessels under sterile conditions with preservation of cellular integrity and vascular contractility. To gain insights into the mechanisms leading to IH, it will now be possible to study vascular remodeling not only under static conditions but also in hemodynamic environment mimicking as closely as possible the flow conditions encountered in reconstructive vascular surgery.