Insulin-inspired hippocampal neuron-targeting technology for protein drug delivery.
Alzheimer’s disease
drug delivery
fusion protein
hippocampal neuron
insulin
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
08 Oct 2024
08 Oct 2024
Historique:
medline:
30
9
2024
pubmed:
30
9
2024
entrez:
30
9
2024
Statut:
ppublish
Résumé
Hippocampal neurons can be the first to be impaired with neurodegenerative disorders, including Alzheimer's disease (AD). Most drug candidates for causal therapy of AD cannot either enter the brain or accumulate around hippocampal neurons. Here, we genetically engineered insulin-fusion proteins, called hippocampal neuron-targeting (Ht) proteins, for targeting protein drugs to hippocampal neurons because insulin tends to accumulate in the neuronal cell layers of the hippocampus. In vitro examinations clarified that insulin and Ht proteins were internalized into the cultured hippocampal neurons through insulin receptor-mediated macropinocytosis. Cysteines were key determinants of the delivery of Ht proteins to hippocampal neurons, and insulin B chain mutant was most potent in delivering cargo proteins. In vivo accumulation of Ht proteins to hippocampal neuronal layers occurred after intracerebroventricular administration. Thus, hippocampal neuron-targeting technology can provide great help for developing protein drugs against neurodegenerative disorders.
Identifiants
pubmed: 39348543
doi: 10.1073/pnas.2407936121
doi:
Substances chimiques
Insulin
0
Recombinant Fusion Proteins
0
Receptor, Insulin
EC 2.7.10.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2407936121Subventions
Organisme : MEXT | Japan Society for the Promotion of Science (JSPS)
ID : 23H03751
Organisme : Takeda Science Foundation (TSF)
ID : NA
Organisme : Mochida Memorial Foundation for Medical and Pharmaceutical Research ( )
ID : NA
Organisme : MEXT | Japan Society for the Promotion of Science (JSPS)
ID : 23K28439
Déclaration de conflit d'intérêts
Competing interests statement:The authors declare no competing interest.