Evidence map›Paper›PMID 28934365›Full record

ArticlePloS one2017

Murine glomerular transcriptome links endothelial cell-specific molecule-1 deficiency with susceptibility to diabetic nephropathy.

Xiaoyi Zheng, Fariborz Soroush, Jin Long, Evan T Hall, Puneeth K Adishesha, Sanchita Bhattacharya, Mohammad F Kiani, Vivek Bhalla

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. 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
0.8field-weighted citation impact, top 29% 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. Esm-1 mediates transcriptional polarization associated with diabetic kidney disease.American journal of physiology. Renal physiology · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Sourcing cells forFrontiers in medical technology · 2022
    Review
  8. Gene expression profiles of diabetic kidney disease and neuropathy in eNOS knockout mice: Predictors of pathology and RAS blockade effects.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. The Role of Endocan in Selected Kidney Diseases.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Review
  16. 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

8 authors at 3 institutions in 1 country.

Xiaoyi ZhengDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Fariborz SoroushDepartment of Mechanical Engineering, College of Engineering, Temple University, Philadelphia, Pennsylvania, United States of America.
Jin LongDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Evan T HallDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Puneeth K AdisheshaDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Sanchita BhattacharyaInstitute of Computational Health Sciences, University of California, San Francisco, California, United States of America.
Mohammad F KianiDepartment of Mechanical Engineering, College of Engineering, Temple University, Philadelphia, Pennsylvania, United States of America.
Vivek BhallaDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID http://orcid.org/0000-0002-5420-9657
Stanford University · USTemple University · USUniversity of California, San Francisco · US

Funding

Coordinating and Bioinformatics Unit for the MMPC/DiaCompU24DK076169 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2006 to 2018
$42.4M
Leukocyte-Endothelial Cell Interactions in SepsisR01GM114359 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI KIANI, MOHAMMAD F, KILPATRICK, LAURIE E · 2015 to 2018
$1.2M
NIDDK NIH HHS U24 DK076169NIGMS NIH HHS R01 GM114359
6 · The paper itself

Abstract

Diabetic nephropathy (DN) is the leading cause of kidney disease; however, there are no early biomarkers and no cure. Thus, there is a large unmet need to predict which individuals will develop nephropathy and to understand the molecular mechanisms that govern this susceptibility. We compared the glomerular transcriptome from mice with distinct susceptibilities to DN at four weeks after induction of diabetes, but before histologic injury, and identified differential regulation of genes that modulate inflammation. From these genes, we identified endothelial cell specific molecule-1 (Esm-1), as a glomerular-enriched determinant of resistance to DN. Glomerular Esm-1 mRNA and protein were lower in DN-susceptible, DBA/2, compared to DN-resistant, C57BL/6, mice. We demonstrated higher Esm-1 secretion from primary glomerular cultures of diabetic mice, and high glucose was sufficient to increase Esm-1 mRNA and protein secretion in both strains of mice. However, induction was significantly attenuated in DN-susceptible mice. Urine Esm-1 was also significantly higher only in DN-resistant mice. Moreover, using intravital microscopy and a biomimetic microfluidic assay, we showed that Esm-1 inhibited rolling and transmigration in a dose-dependent manner. For the first time we have uncovered glomerular-derived Esm-1 as a potential non-invasive biomarker of DN. Esm-1 inversely correlates with disease susceptibility and inhibits leukocyte infiltration, a critical factor in protecting the kidney from DN.

Indexed as

Gene Expression ProfilingGenetic Predisposition to DiseaseAnimalsCell MovementDiabetic NephropathiesDose-Response Relationship, DrugGlucoseHumansKidney GlomerulusLeukocytesMaleMiceNeoplasm ProteinsProteoglycansRNA, MessengerSpecies Specificityendothelial cell-specific molecule-1, mouseESM1 protein, humanGlucoseNeoplasm ProteinsProteoglycansRNA, Messenger

Identifiers

PMID28934365
PMCPMC5608371
OpenAlexW2952301452

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.