Evidence map›Paper›PMID 26136112›Full record

ArticlePloS one2015

Improved Structure and Function in Autosomal Recessive Polycystic Rat Kidneys with Renal Tubular Cell Therapy.

K J Kelly, Jizhong Zhang, Ling Han, Malgorzata Kamocka, Caroline Miller, Vincent H Gattone, Jesus H Dominguez

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 16 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

7 authors at 2 institutions in 1 country.

K J KellyDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Jizhong ZhangDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Ling HanDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Malgorzata KamockaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Caroline MillerDepartment of Anatomy, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Vincent H GattoneDepartment of Anatomy, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Jesus H DominguezDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States of America; Department of Medicine, Veterans Affairs Medical Center, Indianapolis IN, United States of America.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

The Postischemia Inflammatory Syndrome in the Aged KidneyR01DK082739 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI KELLY, KATHERINE J · 2010 to 2014
$1.4M
Mechanisms of Renal Lipotoxicity and Injury in Obesity and DiabetesI01BX000202 · VA · RLR VA MEDICAL CENTER · PI DOMINGUEZ, JESUS H. · 2009 to 2017
–
BLRD VA I01 BX000202NIDDK NIH HHS DK082739NIDDK NIH HHS R01 DK082739
6 · The paper itself

Abstract

Autosomal recessive polycystic kidney disease is a truly catastrophic monogenetic disease, causing death and end stage renal disease in neonates and children. Using PCK female rats, an orthologous model of autosomal recessive polycystic kidney disease harboring mutant Pkhd1, we tested the hypothesis that intravenous renal cell transplantation with normal Sprague Dawley male kidney cells would improve the polycystic kidney disease phenotype. Cytotherapy with renal cells expressing wild type Pkhd1 and tubulogenic serum amyloid A1 had powerful and sustained beneficial effects on renal function and structure in the polycystic kidney disease model. Donor cell engraftment and both mutant and wild type Pkhd1 were found in treated but not control PCK kidneys 15 weeks after the final cell infusion. To examine the mechanisms of global protection with a small number of transplanted cells, we tested the hypothesis that exosomes derived from normal Sprague Dawley cells can limit the cystic phenotype of PCK recipient cells. We found that renal exosomes originating from normal Sprague Dawley cells carried and transferred wild type Pkhd1 mRNA to PCK cells in vivo and in vitro and restricted cyst formation by cultured PCK cells. The results indicate that transplantation with renal cells containing wild type Pkhd1 improves renal structure and function in autosomal recessive polycystic kidney disease and may provide an intra-renal supply of normal Pkhd1 mRNA.

Indexed as

AnimalsCell- and Tissue-Based TherapyCell ProliferationCells, CulturedCystsDisease Models, AnimalExosomesFemaleGenotypeImmunohistochemistryIn Situ Hybridization, FluorescenceKidney TubulesLiverMalePhenotypePolycystic Kidney, Autosomal RecessivePKHD1 protein, ratReceptors, Cell SurfaceRNA, MessengerSerum Amyloid A Protein

Identifiers

PMID26136112
PMCPMC4489886
OpenAlexW2201402672

What OpenQuestion holds

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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.