Evidence map›Paper›PMID 24910411›Full record

ArticleJournal of immunological methods2014

The impact of Nucleofection® on the activation state of primary human CD4 T cells.

Mingce Zhang, Zhengyu Ma, Nithianandan Selliah, Greta Weiss, Anna Genin, Terri H Finkel, Randy Q Cron

Open access · greenAbstract read
In one paragraph

Article in Journal of immunological methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  7. Large-scale manufacturing of base-edited chimeric antigen receptor T cells.Molecular therapy. Methods & clinical development · 2023
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  10. Review
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  12. In vivo imaging of nanoparticle-labeled CAR T cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Challenges of CRISPR-Based Gene Editing in Primary T Cells.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Cas9 RNP transfection by vapor nanobubble photoporation forMolecular therapy. Nucleic acids · 2021
    Article
  17. Article
  18. Microfluidic and Nanofluidic Intracellular Delivery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  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

7 authors at 3 institutions in 1 country.

Mingce ZhangDivision of Pediatric Rheumatology, University of Alabama at Birmingham, 1825 University Blvd,. Shelby Building, Rm. 371, Birmingham, AL 35233, United States. Electronic address: mzhang@peds.uab.edu.
Zhengyu MaNemours/A. I. duPont Hospital for Children, 1600 Rockland Road, Wilmington, DE 19803, United States. Electronic address: zma@nemours.org.
Nithianandan SelliahCelgene Cellular Therapeutics, 7 Powder Horn Dr., Warren, NJ 07059, United States. Electronic address: nithiselliah@gmail.com.
Greta WeissBurnet Institute, 85 Commercial Road, Melbourne, Victoria 3004, Australia. Electronic address: weiss@burnet.edu.au.
Anna GeninDivision of Pediatric Rheumatology, University of Alabama at Birmingham, 1825 University Blvd,. Shelby Building, Rm. 371, Birmingham, AL 35233, United States. Electronic address: agenin@peds.uab.edu.
Terri H FinkelNemours Children's Hospital, 13535 Nemours Parkway, Orlando, FL 32827, United States. Electronic address: tfinkel@nemours.org.
Randy Q CronDivision of Pediatric Rheumatology, University of Alabama at Birmingham, 1825 University Blvd,. Shelby Building, Rm. 371, Birmingham, AL 35233, United States. Electronic address: rcron@peds.uab.edu.
University of Alabama at Birmingham · USCommunity Health Systems - Dupont Hospital · USNemours Children's Clinic · US

Funding

Regulation of CD154 in Systemic Lupus ErythematosusR01AR048257 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CRON, RANDALL Q · 2003 to 2007
$1.6M
Increased HIV-1 Transcription in T-helper 2 CellsR21AI068574 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CRON, RANDALL Q · 2007 to 2008
$395k
Role of NFAT Proteins in CD154 Gene Regulation and LupusR21AR049335 · NIAMS · CHILDREN'S HOSPITAL OF PHILADELPHIA · PI CRON, RANDALL Q · 2002 to 2003
$170k
NIAID NIH HHS R21 AI068574NIAID NIH HHS R21-AI-68574NIAMS NIH HHS R01 AR048257NIAMS NIH HHS R01-AR-48257NIAMS NIH HHS R21 AR049335NIAMS NIH HHS R21-AR-49335
6 · The paper itself

Abstract

Gene transfer into primary human CD4 T lymphocytes is a critical tool in studying the mechanism of T cell-dependent immune responses and human immunodeficiency virus-1 (HIV-1) infection. Nucleofection® is an electroporation technique that allows efficient gene transfer into primary human CD4 T cells that are notoriously resistant to traditional electroporation. Despite its popularity in immunological research, careful characterization of its impact on the physiology of CD4 T cells has not been documented. Herein, using freshly-isolated primary human CD4 T cells, we examine the effects of Nucleofection® on CD4 T cell morphology, intracellular calcium levels, cell surface activation markers, and transcriptional activity. We find that immediately after Nucleofection®, CD4 T cells undergo dramatic morphological changes characterized by wrinkled and dilated plasma membranes before recovering 1h later. The intracellular calcium level also increases after Nucleofection®, peaking after 1h before recovering 8h post transfection. Moreover, Nucleofection® leads to increased expression of T cell activation markers, CD154 and CD69, for more than 24h, and enhances the activation effects of phytohemagglutinin (PHA) stimulation. In addition, transcriptional activity is increased in the first 24h after Nucleofection®, even in the absence of exogenous stimuli. Therefore, Nucleofection® significantly alters the activation state of primary human CD4 T cells. The effect of transferred gene products on CD4 T cell function by Nucleofection® should be assessed after sufficient resting time post transfection or analyzed in light of the activation caveats mentioned above.

Indexed as

ElectroporationLymphocyte ActivationAntigens, CDAntigens, Differentiation, T-LymphocyteCalciumCD40 LigandCD4-Positive T-LymphocytesCD69 AntigensCells, CulturedCell ShapeGene Expression RegulationGenes, ReporterHLA-DR AntigensHumansInterleukin-2 Receptor alpha SubunitLectins, C-TypeAntigens, CDAntigens, Differentiation, T-LymphocyteCalciumCD40 LigandCD69 AntigensHLA-DR AntigensIL2RA protein, humanInterleukin-2 Receptor alpha SubunitLectins, C-TypeCalciumGene transferHIV-1Nucleofection®PlasmidT cell activation

Identifiers

PMID24910411
PMCPMC4120863
OpenAlexW2046361188

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.