Evidence map›Paper›PMID 32238475›Full record

ArticleJournal of the American Society of Nephrology : JASN2020

Exocyst Genes Are Essential for Recycling Membrane Proteins and Maintaining Slit Diaphragm in

Pei Wen, Fujian Zhang, Yulong Fu, Jun-Yi Zhu, Zhe Han

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Life of a Kidney Podocyte.Acta physiologica (Oxford, England) · 2025
    Review
  5. Article
  6. Article
  7. Piezo, Nephrocyte Function, and Slit Diaphragm Maintenance in Drosophila.Journal of the American Society of Nephrology : JASN · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. UsingFrontiers in cell and developmental biology · 2022
    Review
  15. Article
  16. Murine Epsins Play an Integral Role in Podocyte Function.Journal of the American Society of Nephrology : JASN · 2020
    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

5 authors at 1 institution in 2 countries.

Pei WenCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Fujian ZhangCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Yulong FuCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.ORCID 0000-0001-7991-9965
Jun-Yi ZhuCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Zhe HanCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland zhan@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

Modeling Nephrotic Syndrome in Drosophila NephrocytesR01DK098410 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2014 to 2022
$3.3M
Integrating Drosophila and human podocyte studies to discover APOL1 renal toxicity mechanism and therapeutic targetsR01DK120908 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2019 to 2022
$1.4M
NIDDK NIH HHS R01 DK098410NIDDK NIH HHS R01 DK120908
6 · The paper itself

Abstract

backgroundStudies have linked mutations in genes encoding the eight-protein exocyst protein complex to kidney disease, but the underlying mechanism is unclear. Because

methodsWe silenced genes encoding exocyst complex proteins specifically in

resultsSilencing exocyst genes in nephrocytes led to profound changes in structure and function. Abolition of cellular accumulation of hemolymph proteins with dramatically reduced lacuna channel membrane invaginations offered a strong indication of reabsorption defects. Moreover, the slit diaphragm's highly organized surface structure-essential for filtration-was disrupted, and key proteins were mislocalized. Ultrastructural analysis revealed that exocyst gene silencing led to the striking appearance of novel electron-dense structures that we named "exocyst rods," which likely represent accumulated membrane proteins following defective exocytosis or recycling. The slit diaphragm proteins partially colocalized with Sec15, Rab5, and Rab11.

conclusionsOur findings suggest that the slit diaphragm of

Indexed as

EndocytosisAnimalsAnimals, Genetically ModifiedAtrial Natriuretic FactorCell ShapeDextransDrosophila melanogasterDrosophila ProteinsGene SilencingHemolymphMembrane ProteinsMiceMultiprotein ComplexesPodocytesVesicular Transport ProteinsAtrial Natriuretic FactorDextransDrosophila ProteinsMembrane ProteinsMultiprotein ComplexesVesicular Transport Proteinscell biology and structureexocyst complexexocyst rodgenetic renal diseasenephrocyte

Identifiers

PMID32238475
PMCPMC7217423
OpenAlexW3014485882

What Socratic 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 Socratic graph.