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Tissue engineering of heart valves: formation of a three-dimensional tissue using porcine heart valve cells.

作者信息

Rothenburger Markus, Volker Wolfgang, Vischer J Peter, Berendes Elmar, Glasmacher Birgit, Scheld Hans Heinrich, Deiwick Michael

机构信息

Department of Thoracic and Cardiovascular Surgery, Institute for Arteriosclerosis Research, University of Muenster, Germany.

出版信息

ASAIO J. 2002 Nov-Dec;48(6):586-91. doi: 10.1097/00002480-200211000-00003.

Abstract

Tissue engineering is a promising approach to obtaining lifetime durability of heart valves. The goal of this study was to develop a heart valve-like tissue and to compare the ultrastructure with normal valves. Myofibroblasts and endothelial cells were seeded on a type I collagen scaffold. The histologic organization and extracellular matrix were compared in light and electron micrographs. Radiolabeled proteoglycans were characterized by enzymatic degradation experiments. In tissue engineered specimens, cross sectional evaluation revealed that the scaffold (300 microm) was consistently infiltrated with myofibroblasts. Both sides were covered with a multicellular layer of myofibroblasts and overlaid by endothelial cells (50 microm). A newly formed extracellular matrix containing collagen fibrils and proteoglycans was found in the interstitial space. Collagen fibrils with a 60 nm banding pattern were found in both specimens. Small sized proteoglycans (65 nm) were associated and aligned at intervals of 60 nm with collagen fibrils. Large sized proteoglycans (180 nm) were located outside the collagen bundles in amorphous compartments of the extracellular matrix. The majority of glycosaminoglycans were chondroitin/dermatan sulfate, and a minority were heparan sulfate. The morphology and topography of cells and the organization of extracellular matrix in artificial tissues strongly resembles those of native valve tissues.

摘要

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