Evidence map›Paper›PMID 22945766›Full record

ArticleClinical and experimental nephrology2013

Glomerular expression of connexin 40 and connexin 43 in rat experimental glomerulonephritis.

Tetsuo Morioka, Shinichi Okada, Masaaki Nameta, Fadia Kamal, Nadia T Yanakieva-Georgieva, Jian Yao, Ayako Sato, Honglan Piao, Takashi Oite

Abstract read
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In one paragraph

Article in Clinical and experimental nephrology, 2013. 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
0.7field-weighted citation impact, top 32% 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, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Connexin mRNA distribution in adult mouse kidneys.Pflugers Archiv : European journal of physiology · 2021
    Article
  5. Article
  6. Novel Targets for Therapy of Renal Fibrosis.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
    Review
  7. Review
  8. Afadin is localized at cell-cell contact sites in mesangial cells and regulates migratory polarity.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  9. Article
  10. Functional roles of connexins and pannexins in the kidney.Cellular and molecular life sciences : CMLS · 2015
    Review
  11. Review
  12. Connexins and their channels in inflammation.Critical reviews in biochemistry and molecular biology
    Review
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 3 institutions in 1 country.

Tetsuo MoriokaDepartment of Cellular Physiology, Institute of Nephrology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan. tmorioka@d4.dion.ne.jp
Shinichi Okada
Masaaki Nameta
Fadia Kamal
Nadia T Yanakieva-Georgieva
Jian Yao
Ayako Sato
Honglan Piao
Takashi Oite
Niigata University · JPTottori University · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGap junctional intercellular communication is thought to play an important role in the maintenance of cell differentiation and homeostasis. Gap junctions connect glomerular mesangial cells to each other. In this study, we examined the glomerular expression of connexins (Cxs) 40 and 43 at both the protein and transcript levels in anti-Thy1.1 glomerulonephritis (GN).

methodsAnti-Thy1.1 GN was induced by intravenous injection of anti-Thy1.1 monoclonal antibody 1-22-3. Cx protein expression was examined by immunofluorescence, immunoelectron microscopy, and Western blotting. Changes in mRNA levels were detected by real-time reverse transcriptase-polymerase chain reaction.

resultsCx40 was detected in mesangial cells in normal rat glomeruli; its expression was reduced on days 3 and 7 and recovered to normal on day 14 following GN induction. Cx43 was detected in mesangial cells and podocytes in normal rat glomeruli, and its expression did not change during the disease course of GN. Expression of Cx40 and Cx43 was also detected in extraglomerular mesangial cells; this expression did not change during the disease course. Opposing patterns of expression between Cx40 and smooth muscle actin (SMA) were observed with double-immunofluorescence labeling. SMA is a differentiation marker of mesangial cells; it is often expressed during proliferation but not under physiological conditions.

conclusionThese results suggest that Cx40 expression in mesangial cells is related to mesangial cell regeneration. Thus, Cx expression regulation could be a therapeutic target for glomerular diseases.

Indexed as

AnimalsAntibodies, MonoclonalBlotting, WesternConnexin 43ConnexinsFluorescent Antibody TechniqueGap Junction alpha-5 ProteinGlomerulonephritisKidney GlomerulusMaleMicroscopy, ImmunoelectronRatsRats, WistarReal-Time Polymerase Chain ReactionAntibodies, MonoclonalConnexin 43ConnexinsGap Junction alpha-5 Protein

Identifiers

PMID22945766
OpenAlexW2006112542

What OpenQuestion holds

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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.