Evidence map›Paper›PMID 29987489›Full record

ArticleCerebellum (London, England)2019

Intravenously Administered Novel Liposomes, DCL64, Deliver Oligonucleotides to Cerebellar Purkinje Cells.

Ana Tari Ashizawa, Jenny Holt, Kelsey Faust, Weier Liu, Anjana Tiwari, Nan Zhang, Tetsuo Ashizawa

Open access · greenAbstract read
In one paragraph

Article in Cerebellum (London, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Review
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

7 authors at 2 institutions in 1 country.

Ana Tari AshizawaMcKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Jenny HoltMcKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Kelsey FaustMcKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Weier LiuMcKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Anjana TiwariStanley H. Appel Department of Neurology, Houston Methodist Research Institute, 6670 Bertner Avenue, R11-117, Houston, TX, 77030, USA.
Nan ZhangStanley H. Appel Department of Neurology, Houston Methodist Research Institute, 6670 Bertner Avenue, R11-117, Houston, TX, 77030, USA.
Tetsuo AshizawaMcKnight Brain Institute, University of Florida, Gainesville, FL, USA. tashizawa@houstonmethodist.org.ORCID http://orcid.org/0000-0001-7180-2869
University of Florida · USHouston Methodist · US

Funding

Supplementary funding for U01NS104326 Clinical Trial Readiness for SCA1 and SCA3 (“READISCA”)U01NS104326 · NINDS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ASHIZAWA, TETSUO, OZ, GULIN · 2018 to 2022
$6.1M
RNA-Gain-of-Function Pathogenesis in SCA10R01NS083564 · NINDS · UNIVERSITY OF FLORIDA · PI ASHIZAWA, TETSUO · 2013 to 2017
$1.7M
NINDS NIH HHS R01 NS083564NINDS NIH HHS U01 NS104326University of Florida UF Opportunity
6 · The paper itself

Abstract

Cerebellar Purkinje cells (PCs) show conspicuous damages in many ataxic disorders. Targeted delivery of short nucleic acids, such as antisense oligonucleotides, to PCs may be a potential treatment for ataxic disorders, especially spinocerebellar ataxias (SCAs), which are mostly caused by a gain of toxic function of the mutant RNA or protein. However, oligonucleotides do not cross the blood-brain barrier (BBB), necessitating direct delivery into the central nervous system (CNS) through intra-thecal, intra-cisternal, intra-cerebral ventricular, or stereotactic parenchymal administration. We have developed a novel liposome (100 to 200 nm in diameter) formulation, DCL64, composed of dipalmitoyl-phosphatidylcholine, cholesterol, and poloxamer L64, which incorporates oligonucleotides efficiently (≥ 70%). Confocal microscopy showed that DCL64 was selectively taken up by brain microvascular endothelial cells by interacting with low-density lipoprotein receptor (LDLr) family members on cell surface, but not with other types of lipid receptors such as caveolin or scavenger receptor class B type 1. LDLr family members are implicated in brain microvascular endothelial cell endocytosis/transcytosis, and are abundantly localized on cerebellar PCs. Intravenous administration of DCL64 in normal mice showed distribution of oligonucleotides to the brain, preferentially in PCs. Mice that received DCL64 showed no adverse effect on hematological, hepatic, and renal functions in blood tests, and no histopathological abnormalities in major organs. These studies suggest that DCL64 delivers oligonucleotides to PCs across the BBB via intravenous injection with no detectable adverse effects. This property potentially makes DCL64 particularly attractive as a delivery vehicle in treatments of SCAs.

Indexed as

LiposomesAdministration, IntravenousAnimalsCell LineEndothelial CellsFibroblastsHumansMice, Inbred ICRMicrovesselsOligonucleotidesPurkinje CellsReceptors, LDLSpinocerebellar AtaxiasLiposomesOligonucleotidesReceptors, LDLBlood-brain barrierLiposomesLow-density lipoprotein receptorOligonucleotidePurkinje cellsSpinocerebellar ataxias

Identifiers

PMID29987489
PMCPMC6326905
OpenAlexW2875658289

What OpenQuestion holds

Textmetadata
LicenceTDM
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.