Evidence map›Paper›PMID 37729550›Full record

ArticleBiochemistry2023

Lipid Nanoparticles Deliver mRNA to the Brain after an Intracerebral Injection.

Jan Tuma, Yu-Ju Chen, Michael G Collins, Abhik Paul, Jie Li, Hesong Han, Rohit Sharma, Niren Murthy, Hye Young Lee

Open access · greenAbstract read
In one paragraph

Article in Biochemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Single-ligand dual-targeting lipid nanoparticles for therapeutic mRNA delivery to glioblastoma across the blood-brain barrier.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  5. Review
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  8. Review
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  15. Article
  16. Rational design of lipid nanoparticles for enabling gene therapies.Molecular therapy. Methods & clinical development · 2025
    Review
  17. Harnessing mRNA-lipid nanoparticles as innovative therapies for autoimmune diseases.Molecular therapy. Methods & clinical development · 2025
    Review
  18. Article
  19. Article
  20. 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

9 authors at 2 institutions in 2 countries.

Jan TumaThe Department of Cellular and Integrative Physiology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, United States.ORCID 0000-0002-7197-8482
Yu-Ju ChenThe Department of Cellular and Integrative Physiology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, United States.ORCID 0000-0002-1197-1086
Michael G CollinsThe Department of Cellular and Integrative Physiology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, United States.ORCID 0000-0002-3161-0595
Abhik PaulThe Department of Cellular and Integrative Physiology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, United States.ORCID 0000-0003-3797-2439
Jie LiDepartment of Bioengineering, University of California, Berkeley, California 94720, United States.ORCID 0000-0003-0189-2787
Hesong HanDepartment of Bioengineering, University of California, Berkeley, California 94720, United States.ORCID 0000-0001-5545-5238
Rohit SharmaDepartment of Bioengineering, University of California, Berkeley, California 94720, United States.ORCID 0000-0003-1428-5521
Niren MurthyDepartment of Bioengineering, University of California, Berkeley, California 94720, United States.ORCID 0000-0002-7815-7337
Hye Young LeeThe Department of Cellular and Integrative Physiology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, United States.ORCID 0000-0002-3150-6886
The University of Texas Health Science Center at San Antonio · USInnovative Genomics Institute · US

Funding

HOPE - HIV Obstruction by Programmed EpigeneticsUM1AI164559 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI Lishomwa C Ndhlovu, Melanie Maria Ott · 2021 to 2026
$32.2M
Resource Core II: In Vivo CoreU19NS132303 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI FYODOR D URNOV · 2023 to 2026
$19.7M
Gene editing in the brain with CRISPR-PEGR01MH125979 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LEE, HYE YOUNG, MURTHY, NIREN · 2021 to 2025
$3.3M
Imaging bacterial infections with 2nd generation maltodextrinsR01EB029320 · NIBIB · EMORY UNIVERSITY · PI GOODMAN, MARK MYRON, MURTHY, NIREN · 2020 to 2023
$2.7M
Development of a Nanoparticle-Based Gene Editing Technology for Neurological ApplicationsUG3NS115599 · NINDS · OHIO STATE UNIVERSITY · PI BANKIEWICZ, KRYSTOF S, MURTHY, NIREN · 2019 to 2021
$2.3M
Single-Cell Transcriptomics of Non-Activated Latently Infected T cells Isolated from HIV+ Drug UsersR33DA048444 · NIDA · J. DAVID GLADSTONE INSTITUTES · PI OTT, MELANIE MARIA · 2022 to 2023
$1.9M
Maltose Targeted AntibioticsR33AI119115 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI MURTHY, NIREN, RILEY, LEE W · 2017 to 2019
$1.4M
Investigating CD33 function on microglia during Alzheimer’s disease using CRISPR nanoparticlesR21AG072423 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HOPP, SARAH CHRISTINE · 2021 to 2021
$426k
NIAID NIH HHS R33 AI119115NIAID NIH HHS UM1 AI164559NIA NIH HHS R21 AG072423NIBIB NIH HHS R01 EB029320NIDA NIH HHS R33 DA048444NIMH NIH HHS R01 MH125979NINDS NIH HHS U19 NS132303NINDS NIH HHS UG3 NS115599
6 · The paper itself

Abstract

Neurological disorders are often debilitating conditions with no cure. The majority of current therapies are palliative rather than disease-modifying; therefore, new strategies for treating neurological disorders are greatly needed. mRNA-based therapeutics have great potential for treating such neurological disorders; however, challenges with delivery have limited their clinical potential. Lipid nanoparticles (LNPs) are a promising delivery vector for the brain, given their safer toxicity profile and higher efficacy. Despite this, very little is known about LNP-mediated delivery of mRNA into the brain. Here, we employ MC3-based LNPs and successfully deliver Cre mRNA and Cas9 mRNA/Ai9 sgRNA to the adult Ai9 mouse brain; greater than half of the entire striatum and hippocampus was found to be penetrated along the rostro-caudal axis by direct intracerebral injections of MC3 LNP mRNAs. MC3 LNP Cre mRNA successfully transfected cells in the striatum (∼52% efficiency) and hippocampus (∼49% efficiency). In addition, we demonstrate that MC3 LNP Cas9 mRNA/Ai9 sgRNA edited cells in the striatum (∼7% efficiency) and hippocampus (∼3% efficiency). Further analysis demonstrates that MC3 LNPs mediate mRNA delivery to multiple cell types including neurons, astrocytes, and microglia in the brain. Overall, LNP-based mRNA delivery is effective in brain tissue and shows great promise for treating complex neurological disorders.

Indexed as

NanoparticlesNervous System DiseasesAnimalsBrainLiposomesMiceRNA, Guide, CRISPR-Cas SystemsRNA, MessengerRNA, Small InterferingLipid NanoparticlesLiposomesRNA, Guide, CRISPR-Cas SystemsRNA, MessengerRNA, Small Interfering

Identifiers

PMID37729550
PMCPMC10760911
OpenAlexW4386884157

What OpenQuestion holds

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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.