Rat heart perfusion as model system for enzyme replacement therapy in glycogenosis type II

Abstract

Cardiac failure and skeletal muscle weakness are the main clinical features of glycogenosis type II, a lysosomal storage disorder caused by acid α-glucosidase deficiency. In our study, we have investigated in a rat heart perfusion-recirculation system whether acid α-glucosidase can be taken up from the vascular system into cardiomy-ocytes. When rat hearts were perfused with mannose 6-phosphate-containing acid α-glucosidase purified from bovine testis, a 3- to 4-fold increase of enzyme activity was obtained. Perfusion with human placental acid α-glucosidase not containing the mannose 6-phosphate recognition marker did not have such an effect. The presence of bovine testis acid α-glucosidase in heart tissue was demonstrated by immunoblotting. Immunocytochemistry provides evidence for uptake of the exogenous enzyme in lysosomes of the cardiomyocytes. The relevance of these findings for enzyme therapy in glycogenosis type II is discussed. © 1990 International Pediatric Research Foundation, Inc.