Comparison of five peptide vectors for improved brain delivery of the lysosomal enzyme arylsulfatase A

• Published in: The Journal of neuroscience 2014-02, Vol.34 (9), p.3122-3129
• Main Authors: Böckenhoff, Annika, Cramer, Sandra, Wölte, Philipp, Knieling, Simeon, Wohlenberg, Claudia, Gieselmann, Volkmar, Galla, Hans-Joachim, Matzner, Ulrich
• Format: Article
• Language: English
• Subjects: Animals; Apolipoproteins E - genetics; Blood-Brain Barrier - drug effects; Blood-Brain Barrier - metabolism; Brain - cytology; Brain - metabolism; Cells, Cultured; Cerebroside-Sulfatase - administration & dosage; Cerebroside-Sulfatase - deficiency; Cerebroside-Sulfatase - genetics; Cricetulus; Culture Media, Conditioned - pharmacology; Disease Models, Animal; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Female; Genetic Vectors - physiology; Human immunodeficiency virus; Humans; Leukodystrophy, Metachromatic - drug therapy; Leukodystrophy, Metachromatic - pathology; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Peptides - metabolism; Receptor, IGF Type 2 - genetics; Receptor, IGF Type 2 - metabolism; Recombinant Fusion Proteins - genetics; Recombinant Fusion Proteins - metabolism
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.4785-13.2014

Enzyme replacement therapy (ERT) is a treatment option for lysosomal storage disorders (LSDs) caused by deficiencies of soluble lysosomal enzymes. ERT depends on receptor-mediated transport of intravenously injected recombinant enzyme to lysosomes of patient cells. The blood-brain barrier (BBB) prevents efficient transfer of therapeutic polypeptides from the blood to the brain parenchyma and thus hinders effective treatment of LSDs with CNS involvement. We compared the potential of five brain-targeting peptides to promote brain delivery of the lysosomal enzyme arylsulfatase A (ASA). Fusion proteins between ASA and the protein transduction domain of the human immunodeficiency virus TAT protein (Tat), an Angiopep peptide (Ang-2), and the receptor-binding domains of human apolipoprotein B (ApoB) and ApoE (two versions, ApoE-I and ApoE-II) were generated. All ASA fusion proteins were enzymatically active and targeted to lysosomes when added to cultured cells. In contrast to wild-type ASA, which is taken up by mannose-6-phosphate receptors, all chimeric proteins were additionally endocytosed via mannose-6-phosphate-independent routes. For ASA-Ang-2, ASA-ApoE-I, and ASA-ApoE-II, uptake was partially due to the low-density lipoprotein receptor-related protein 1. Transendothelial transfer in a BBB cell culture model was elevated for ASA-ApoB, ASA-ApoE-I, and ASA-ApoE-II. Brain delivery was, however, increased only for ASA-ApoE-II. ApoE-II was also superior to wild-type ASA in reducing lysosomal storage in the CNS of ASA-knock-out mice treated by ERT. Therefore, the ApoE-derived peptide appears useful to treat metachromatic leukodystrophy and possibly other neurological disorders more efficiently.