Feasibility Study of Dendrimer-Based TTR-CRISPR pDNA Polyplex for Ocular Amyloidosis in Vitro

• Published in: Biological & pharmaceutical bulletin Vol. 45; no. 11; pp. 1660 - 1668
• Main Authors: Inoue, Masamichi, Muta, Kyosuke, Mohammed, Ahmed Fouad Abdelwahab, Onodera, Risako, Higashi, Taishi, Ouchi, Kenta, Ueda, Mitsuharu, Ando, Yukio, Arima, Hidetoshi, Jono, Hirofumi, Motoyama, Keiichi
• Format: Journal Article
• Language: English
• Published: Tokyo The Pharmaceutical Society of Japan 01.11.2022; Japan Science and Technology Agency
• Subjects: Amyloid; Amyloidosis; CRISPR; cyclodextrin; dendrimer; Feasibility studies; Folic acid; Gene transfer; Genetic disorders; Genomes; Point mutation; Retina; Retinal pigment epithelium; Transthyretin; Vitamin B; β-Cyclodextrin
• ISSN: 0918-6158; 1347-5215
• DOI: 10.1248/bpb.b22-00452

Hereditary amyloidgenic transthyretin (ATTR) amyloidosis is caused by a genetic point-mutated transthyretin such as TTR Val30Met (TTR V30M), since it forms protein aggregates called amyloid resulting in the tissue accumulation and functional disorders. In particular, ATTR produced by retinal pigment epithelial cells often causes ATTR ocular amyloidosis, which elicits deterioration of ocular function and ultimately blindness. Therefore, development of novel therapeutic agents is urgently needed. Genome-editing technology using Clustered Regularly Interspaced Short Palindromic Repeats-CRISPR associated proteins (CRISPR-Cas9) system is expected to be a therapeutic approach to treat genetic diseases, such as ATTR amyloidosis caused by a point mutation in TTR gene. Previously, we reported that glucuronylglucosyl-β-cyclodextrin conjugated with a polyamidoamine dendrimer (CDE) had excellent gene transfer ability and that underlying dendrimer inhibited TTR aggregation. Conversely, folate receptors are known to be highly expressed in retina; thus, folate has potential as a retinal target ligand. In this study, we prepared a novel folate-modified CDE (FP-CDE) and investigated its potential as a carrier for the retinal delivery of TTR-CRISPR plasmid DNA (pDNA). The results suggested that FP-CDE/TTR-CRISPR pDNA could be taken up by retinal pigment epithelial cells via folate receptors, exhibited TTR V30M amyloid inhibitory effect, and suppressed TTR production via the genome editing effect (knockout of TTR gene). Thus, FP-CDE may be useful as a novel therapeutic TTR-CRISPR pDNA carrier in the treatment of ATTR ocular amyloidosis.