DNA and cell biology reports · 2025
Correction of Disease Phenotype in Pompe Disease Knockout Mice Following Cationic Lipid-GL-67-Mediated Gene Therapy.
СтатьяНазвание и аннотация: Перевод в очереди
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Martiniuk Frank, Martiniuk Justin, Mack Adra, Cheng Seng H
Аннотация
BACKGROUND: Genetic deficiency of lysosomal acid α-glucosidase or acid maltase (GAA) results in Pompe disease (PD) or glycogen storage disease type II, encompassing subtypes of varying severity. The infantile form presents as hypotonia, muscle weakness, and congestive heart failure in the first year, while the adult onset forms are limited to skeletal muscle. Gene therapy for diseases that affect muscles or organs (as PD) may be very difficult due to their size or location and our ability to transfect these organs with high efficiency.
METHODS: We evaluated a plasmid vector carrying the cytomegalovirus promoter linked to the human GAA cDNA complexed with the cationic lipid GL-67 as a delivery system for therapy of PD.
RESULTS: A human PD fibroblast cell line was transiently transfected with increasing amounts of the cationic lipid GL-67 complexed to the human GAA expression plasmid. Cells showed a significant increase in human GAA activity with 20 nmol of the cationic lipid, resulting in maximal expression. GAA knockout mice were treated intraperitoneally every 2 weeks for four months with 100 µg of plasmid and 2 mM GL-67 lipid. Tissues, including heart, diaphragm, and skeletal muscle showed substantial increase in GAA activity. More important, the clinical phenotype of hind and forelimb muscle weakness was reversed and life span extended to almost normal longevity.
CONCLUSIONS: These data suggest that cationic lipid mediated gene delivery of the human GAA cDNA may be an effective treatment for PD.
METHODS: We evaluated a plasmid vector carrying the cytomegalovirus promoter linked to the human GAA cDNA complexed with the cationic lipid GL-67 as a delivery system for therapy of PD.
RESULTS: A human PD fibroblast cell line was transiently transfected with increasing amounts of the cationic lipid GL-67 complexed to the human GAA expression plasmid. Cells showed a significant increase in human GAA activity with 20 nmol of the cationic lipid, resulting in maximal expression. GAA knockout mice were treated intraperitoneally every 2 weeks for four months with 100 µg of plasmid and 2 mM GL-67 lipid. Tissues, including heart, diaphragm, and skeletal muscle showed substantial increase in GAA activity. More important, the clinical phenotype of hind and forelimb muscle weakness was reversed and life span extended to almost normal longevity.
CONCLUSIONS: These data suggest that cationic lipid mediated gene delivery of the human GAA cDNA may be an effective treatment for PD.