Evidence map›Paper›PMID 29058957›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2017

CTGF Is Expressed During Cystic Remodeling in the PKD/Mhm (cy/+) Rat Model for Autosomal-Dominant Polycystic Kidney Disease (ADPKD).

Stefan Gauer, Yvonne Holzmann, Bettina Kränzlin, Sigrid C Hoffmann, Norbert Gretz, Ingeborg A Hauser, Margarete Goppelt-Struebe, Helmut Geiger, Nicholas Obermüller

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. 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 5 institutions in 1 country.

Stefan GauerDepartment of Nephrology, Medical Clinic III, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Yvonne HolzmannDepartment of Nephrology, Medical Clinic III, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Bettina KränzlinMedical Research Center, University of Heidelberg, Mannheim, Germany.
Sigrid C HoffmannMedical Research Center, University of Heidelberg, Mannheim, Germany.
Norbert GretzMedical Research Center, University of Heidelberg, Mannheim, Germany.
Ingeborg A HauserDepartment of Nephrology, Medical Clinic III, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Margarete Goppelt-StruebeDepartment of Nephrology and Hypertension, Medical Clinic 4, University of Erlangen-Nuremberg, Erlangen, Germany.
Helmut GeigerDepartment of Nephrology, Medical Clinic III, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Nicholas ObermüllerDepartment of Nephrology, Medical Clinic III, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Goethe University Frankfurt · DEHeidelberg University · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity Hospital Frankfurt · DEUniversity Medical Centre Mannheim · DE

Funding

A SAM domain network in Polycystic Kidney DiseaseR01DK100482 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BOWIE, JAMES U · 2014 to 2017
$1.1M
NIDDK NIH HHS R01 DK100482
6 · The paper itself

Abstract

Connective tissue growth factor (CTGF, also named CCN2) plays an important role in the development of tubulointerstitial fibrosis, which most critically determines the progression to end-stage renal failure in autosomal-dominant polycystic kidney disease (ADPKD), the most common genetically caused renal disease. We determined CTGF expression in a well-characterized animal model of human ADPKD, the PKD/Mhm (cy/+) rat. Kidneys of 12 weeks old (cy/+) as well as (+/+) non-affected rats were analyzed for CTGF RNA and protein expression by RT-PCR, Northern and Western blot analyses, in situ hybridization, and IHC. Besides the established expression of CTGF in glomerular cells in kidneys of wild-type (+/+) animals, in (cy/+) rats, CTGF mRNA and protein were robustly expressed in interstitial, stellate-shaped cells, located in a scattered pattern underlying the cystic epithelium and in focal areas of advanced tubulointerstitial remodeling. Renal CTGF mRNA and protein expression levels were significantly higher in (cy/+) rats compared with their (+/+) littermates. Detection of CTGF expression in cells adjacent to cystic epithelium and in areas of marked fibrosis suggests a role in the local response to cyst development and indicates that CTGF may be a relevant factor contributing to tubulointerstitial fibrosis in polycystic kidney disease.

Indexed as

Gene Expression RegulationAnimalsConnective Tissue Growth FactorDisease Models, AnimalFibrosisKidneyMalePolycystic Kidney, Autosomal DominantRatsRNA, MessengerConnective Tissue Growth FactorRNA, MessengerCCN2fibrosisinterstitial cellspolycystic kidney diseaserenal failure

Identifiers

PMID29058957
PMCPMC5714099
OpenAlexW2765126794

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.