Evidence map›Paper›PMID 29364221›Full record

ArticleJournal of visualized experiments : JoVE2018

Hydrodynamic Renal Pelvis Injection for Non-viral Expression of Proteins in the Kidney.

Lauren E Woodard, Richard C Welch, Felisha M Williams, Wentian Luo, Jizhong Cheng, Matthew H Wilson

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 10 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Lauren E WoodardDepartment of Veterans Affairs, Tennessee Valley Healthcare System; Departments of Medicine and Pharmacology, Vanderbilt University Medical Center; Department of Medicine, Baylor University College of Medicine.
Richard C WelchDepartments of Medicine and Pharmacology, Vanderbilt University Medical Center.
Felisha M WilliamsDepartments of Medicine and Pharmacology, Vanderbilt University Medical Center.
Wentian LuoDepartments of Medicine and Pharmacology, Vanderbilt University Medical Center.
Jizhong ChengDepartment of Medicine, Baylor University College of Medicine.
Matthew H WilsonDepartment of Veterans Affairs, Tennessee Valley Healthcare System; Departments of Medicine and Pharmacology, Vanderbilt University Medical Center; Department of Medicine, Baylor University College of Medicine; matthew.wilson@vanderbilt.edu.
Vanderbilt University Medical Center · USBaylor University · US

Funding

Novel cell therapy for sustained therapeutic protein delivery in vivoR01DK093660 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WILSON, MATTHEW H · 2012 to 2022
$3.4M
CHRONIC KIDNEY DISEASE ADVERSELY INFLUENCES VASCULAR FUNCTIONSR01DK095867 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHENG, JIZHONG · 2013 to 2017
$1.7M
Replacement and Upgrade of an Optical Imaging System for Small AnimalsS10OD021804 · OD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORE, JOHN C · 2017 to 2017
$409k
Kidney specific site-directed integration for cystinuriaI01BX002190 · VA · VETERANS HEALTH ADMINISTRATION · PI WILSON, MATTHEW H · 2014 to 2017
–
In Situ Reprogramming of Induced Nephron Progenitor Cells for Kidney RegenerationIK2BX002797 · VA · VETERANS HEALTH ADMINISTRATION · PI WOODARD, LAUREN ELIZABETH · 2015 to 2020
–
BLRD VA I01 BX002190BLRD VA IK2 BX002797NIDDK NIH HHS R01 DK093660NIDDK NIH HHS R01 DK095867NIH HHS S10 OD021804
6 · The paper itself

Abstract

Hydrodynamic injection creates a local, high-pressure environment to transfect various tissues with plasmid DNA and other substances. Hydrodynamic tail vein injection, for example, is a well-established method by which the liver can be transfected. This manuscript describes an application of hydrodynamic principles by injection of the mouse kidney directly with plasmid DNA for kidney-specific gene expression. Mice are anesthetized and the kidney is exposed by a flank incision followed by a fast injection of a plasmid DNA-containing solution directly into the renal pelvis. The needle is kept in place for ten seconds and the incision site is sutured. The following day, live animal imaging, Western blot, or immunohistochemistry may be used to assay gene expression, or other assays suited to the transgene of choice are used for detection of the protein of interest. Published methods to prolong gene expression include transposon-mediated transgene integration and cyclophosphamide treatment to inhibit the immune response to the transgene.

Indexed as

AnimalsDNAHydrodynamicsInjectionsKidneyKidney PelvisMaleMicePlasmidsProtein BiosynthesisTransfectionTransgenesDNA

Identifiers

PMID29364221
PMCPMC5907682
OpenAlexW2782975620

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.