Evidence map›Paper›PMID 31426598›Full record

ArticleMolecules (Basel, Switzerland)2019

Development of Organelle Replacement Therapy Using a Stearyl-Polyhistidine Peptide against Lysosomal Storage Disease Cells.

Taiki Hayashi, Riku Okamoto, Tsuyoshi Kawano, Takashi Iwasaki

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Zebra-Sphinx: Modeling Sphingolipidoses in Zebrafish.International journal of molecular sciences · 2023
    Review
  2. Review
  3. Reduced α-galactosidase A activity in zebrafish (Molecular genetics and metabolism reports · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Taiki HayashiDepartment of Agricultural Science, Graduate School of Sustainability Science, Tottori University, Tottori 680-8553, Japan.
Riku OkamotoDepartment of Bioresources Science, Faculty of Agriculture, Tottori University, Tottori 680-8553, Japan.
Tsuyoshi KawanoDepartment of Agricultural Science, Graduate School of Sustainability Science, Tottori University, Tottori 680-8553, Japan.
Takashi IwasakiDepartment of Agricultural Science, Graduate School of Sustainability Science, Tottori University, Tottori 680-8553, Japan. itaka@tottori-u.ac.jp.
Tottori University · JP

Funding

Japan Society for the Promotion of Science 15K18689
6 · The paper itself

Abstract

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.

Indexed as

Drug CarriersBiological TransportCell EngineeringCell LineCell Line, TumorCell-Penetrating PeptidesCell ProliferationFabry DiseaseFibroblastsGene ExpressionHistidineHumansHydrophobic and Hydrophilic InteractionsLuminescent ProteinsLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsCell-Penetrating PeptidesDrug CarriersHistidineLAMP1 protein, humanLuminescent ProteinsLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinspolyhistidineRecombinant Fusion ProteinsRed Fluorescent Proteincell-penetrating peptidedrug delivery systemFabry diseasehistidinelysosomelysosome storage disease

Identifiers

PMID31426598
PMCPMC6720886
OpenAlexW2967693865

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.