Development of Organelle Replacement Therapy Using a Stearyl-Polyhistidine Peptide against Lysosomal Storage Disease Cells.
Biological Transport
Cell Engineering
/ methods
Cell Line
Cell Line, Tumor
Cell Proliferation
Cell-Penetrating Peptides
/ chemical synthesis
Drug Carriers
Fabry Disease
/ pathology
Fibroblasts
/ metabolism
Gene Expression
Histidine
/ chemical synthesis
Humans
Hydrophobic and Hydrophilic Interactions
Luminescent Proteins
/ genetics
Lysosomal Membrane Proteins
/ genetics
Lysosomes
/ chemistry
Models, Biological
Molecular Targeted Therapy
/ methods
Recombinant Fusion Proteins
/ genetics
Red Fluorescent Protein
Fabry disease
cell-penetrating peptide
drug delivery system
histidine
lysosome
lysosome storage disease
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
18 Aug 2019
18 Aug 2019
Historique:
received:
11
07
2019
revised:
16
08
2019
accepted:
17
08
2019
entrez:
21
8
2019
pubmed:
21
8
2019
medline:
17
1
2020
Statut:
epublish
Résumé
We previously reported on a polyhistidine peptide, His16 peptide, as a new cell-penetrating peptide. This peptide is anticipated to be a new carrier for drug delivery systems (DDSs) for targeting intracellular lysosomes because it can transport macromolecules (e.g., liposomes) into these organelles. In the present study, we examined the application of His16 peptide as a DDS carrier against lysosomal storage disease (LSD) cells. LSDs are metabolic disorders caused by loss of specific lysosomal enzymes. For the treatment of LSD cells, we devised a system designated organelle replacement therapy (ORT). ORT is a strategy for transporting exogenous lysosomes containing all kinds of lysosomal enzymes from normal cells into endogenous lysosomes in LSD cells using His16 peptide. To develop the ORT system, we prepared His16 peptide-modified healthy lysosomes (His16-Lyso) by insertion of a stearyl-His16 peptide into a hydrophobic region in the lysosomal membrane. His16-Lyso showed cellular uptake and localization to endogenous lysosomes in LSD cells. His16-Lyso also restored the proliferation of LSD cells, which otherwise showed slower proliferation than normal cells. These results suggested that His16-Lyso replenished deficient lysosomal enzymes in LSD cells. The results further suggest that His16-Lyso are promising candidates as a treatment tool for LSD cells and to establish a foundation for ORT.
Identifiants
pubmed: 31426598
pii: molecules24162995
doi: 10.3390/molecules24162995
pmc: PMC6720886
pii:
doi:
Substances chimiques
Cell-Penetrating Peptides
0
Drug Carriers
0
LAMP1 protein, human
0
Luminescent Proteins
0
Lysosomal Membrane Proteins
0
Recombinant Fusion Proteins
0
polyhistidine
26062-48-6
Histidine
4QD397987E
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Japan Society for the Promotion of Science
ID : 15K18689
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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