Evidence map›Paper›PMID 32358194›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Acoustofluidic sonoporation for gene delivery to human hematopoietic stem and progenitor cells.

Jason N Belling, Liv K Heidenreich, Zhenhua Tian, Alexandra M Mendoza, Tzu-Ting Chiou, Yao Gong, Natalie Y Chen, Thomas D Young, Natcha Wattanatorn, Jae Hyeon Park and 9 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
6.4field-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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 122 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Reconfigurable Acoustofluidic Microvortices for Selective Microcargo Delivery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Article
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  8. Review
  9. The Rise of Mechanobiology for Advanced Cell Engineering and Manufacturing.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
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  13. Article
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  15. Article
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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

19 authors at 4 institutions in 1 country.

Jason N BellingCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-7750-5689
Liv K HeidenreichCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-9724-1158
Zhenhua TianDepartment of Mechanical Engineering and Material Science, Duke University, Durham, NC 27707.ORCID 0000-0002-1903-5604
Alexandra M MendozaCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0003-3359-6077
Tzu-Ting ChiouDepartment of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.ORCID 0000-0003-0348-8147
Yao GongCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-6434-9998
Natalie Y ChenDepartment of Medicine and the Molecular Biology Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0002-8961-6244
Thomas D YoungCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0002-3234-7418
Natcha WattanatornCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-5135-7761
Jae Hyeon ParkCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0002-2266-943X
Leonardo ScarabelliCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0002-6830-5893
Naihao ChiangCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0003-3782-6546
Jack TakahashiCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-7196-7436
Stephen G YoungDepartment of Medicine and the Molecular Biology Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-7270-3176
Adam Z StiegCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095.ORCID 0000-0001-7312-9364
Satiro De OliveiraDepartment of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.ORCID 0000-0002-8181-7316
Tony Jun HuangDepartment of Mechanical Engineering and Material Science, Duke University, Durham, NC 27707.ORCID 0000-0003-1205-3313
Paul S WeissCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095; psw@cnsi.ucla.edu sjjonas@mednet.ucla.edu.ORCID 0000-0001-5527-6248
Steven J JonasCalifornia NanoSystems Institute, University of California, Los Angeles, CA 90095; psw@cnsi.ucla.edu sjjonas@mednet.ucla.edu.ORCID 0000-0002-8111-0249
California NanoSystems Institute · USChildren’s Institute · USDuke University · USUniversity of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 1991 to 2018
$39.9M
UC BRAID Center for Accelerated Innovation COVID-19 diagnostic project developmentU54HL119893 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PALAZZOLO, MICHAEL J · 2013 to 2020
$18.3M
The Effect of Nanoparticle Encapsulated Resveratrol on Treatment of PeriodontitisKL2TR001882 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Elizabeta Nemeth · 2016 to 2026
$13.1M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
Nanoscience-Inspired Acoustofluidic Assembly Lines for Gene and Cellular TherapiesDP5OD028181 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONAS, STEVEN JOHN · 2019 to 2023
$1.9M
Enabling Efficient, Fast, Biocompatible Exosome Separation via AcoustofluidicsR01GM132603 · NIGMS · DUKE UNIVERSITY · PI HUANG, TONY JUN · 2019 to 2022
$1.7M
Determining treatment sensitivity in B cell lymphoma by novel microfluidics-based NK cell immunogenicity platformR33CA223908 · NCI · NORTHEASTERN UNIVERSITY · PI EVENS, ANDREW M, HUANG, TONY JUN · 2018 to 2020
$1.2M
An integrated acoustofluidic droplet-sorting platform for classification of lymphocyte activity and functional phenotyping at single cell levelR01GM127714 · NIGMS · NORTHEASTERN UNIVERSITY · PI KONRY, TANIA TALI · 2018 to 2021
$1.2M
Engineering Precision Medicine to Enhance Graft-Versus-Lymphoma EffectK23CA222659 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DE OLIVEIRA, SATIRO NAKAMURA · 2017 to 2022
$920k
Site-Specific Correction of Sickle Cell Disease Using Acoustofludic Gene DeliveryF31HL149356 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BELLING, JASON NATHANIEL · 2019 to 2020
$71k
NCATS NIH HHS KL2 TR001882NCATS NIH HHS UL1 TR001881NCI NIH HHS K23 CA222659NCI NIH HHS P30 CA016042NCI NIH HHS R33 CA223908NHLBI NIH HHS F31 HL149356NHLBI NIH HHS T32 HL069766NHLBI NIH HHS U54 HL119893NIAID NIH HHS P30 AI028697NIGMS NIH HHS R01 GM127714NIGMS NIH HHS R01 GM132603NIH HHS DP5 OD028181
6 · The paper itself

Abstract

Advances in gene editing are leading to new medical interventions where patients' own cells are used for stem cell therapies and immunotherapies. One of the key limitations to translating these treatments to the clinic is the need for scalable technologies for engineering cells efficiently and safely. Toward this goal, microfluidic strategies to induce membrane pores and permeability have emerged as promising techniques to deliver biomolecular cargo into cells. As these technologies continue to mature, there is a need to achieve efficient, safe, nontoxic, fast, and economical processing of clinically relevant cell types. We demonstrate an acoustofluidic sonoporation method to deliver plasmids to immortalized and primary human cell types, based on pore formation and permeabilization of cell membranes with acoustic waves. This acoustofluidic-mediated approach achieves fast and efficient intracellular delivery of an enhanced green fluorescent protein-expressing plasmid to cells at a scalable throughput of 200,000 cells/min in a single channel. Analyses of intracellular delivery and nuclear membrane rupture revealed mechanisms underlying acoustofluidic delivery and successful gene expression. Our studies show that acoustofluidic technologies are promising platforms for gene delivery and a useful tool for investigating membrane repair.

Indexed as

Gene Transfer TechniquesHematopoietic SystemStem CellsCell SurvivalCytoplasmGene ExpressionGenetic TherapyGreen Fluorescent ProteinsHematopoietic Stem Cell TransplantationHumansJurkat CellsPlasmidsSoundenhanced green fluorescent proteinGreen Fluorescent Proteinsacoustofluidicsgene therapyhematopoietic stem cellsintracellular delivery

Identifiers

PMID32358194
PMCPMC7245081
OpenAlexW3021671449

What OpenQuestion holds

Textmetadata
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.