Evidence map›Paper›PMID 26887834›Full record

ArticleAmerican journal of physiology. Renal physiology2016

Mechanism of increased clearance of glycated albumin by proximal tubule cells.

Mark C Wagner, Jered Myslinski, Shiv Pratap, Brittany Flores, George Rhodes, Silvia B Campos-Bilderback, Ruben M Sandoval, Sudhanshu Kumar, Monika Patel, Ashish and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  11. The Indiana O'Brien Center for Advanced Renal Microscopic Analysis.American journal of physiology. Renal physiology · 2021
    Review
  12. Article
  13. Review
  14. Human serum albumin presents isoform variants with altered neonatal Fc receptor interactions.Protein science : a publication of the Protein Society · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. L-Asparaginase of Leishmania donovani: Metabolic target and its role in Amphotericin B resistance.International journal for parasitology. Drugs and drug resistance · 2017
    Article
  19. Review
  20. Intravital imaging of the kidney in a rat model of salt-sensitive hypertension.American journal of physiology. Renal physiology · 2017
    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

11 authors at 3 institutions in 2 countries.

Mark C WagnerNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Jered MyslinskiNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Shiv PratapThe Council of Scientific and Industrial Research Institute of Microbial Technology, Chandigarh, India.
Brittany FloresNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
George RhodesNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Silvia B Campos-BilderbackNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Ruben M SandovalNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Sudhanshu KumarNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
Monika PatelNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and.
AshishThe Council of Scientific and Industrial Research Institute of Microbial Technology, Chandigarh, India.
Bruce A MolitorisNephrology Division, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; and Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana; Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana; and bmolitor@iu.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineInstitute of Microbial Technology · IN

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
PROBE DELIVERY COREP30DK079312 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MOLITORIS, BRUCE A · 2007 to 2021
$17.1M
Proximal Tubule Albumin Transport in Disease States.R01DK091623 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI MOLITORIS, BRUCE A · 2011 to 2021
$4.3M
NIDDK NIH HHS P30 DK079312NIDDK NIH HHS P30 DK097512NIDDK NIH HHS R01 DK091623
6 · The paper itself

Abstract

Serum albumin is the most abundant plasma protein and has a long half-life due to neonatal Fc receptor (FcRn)-mediated transcytosis by many cell types, including proximal tubule cells of the kidney. Albumin also interacts with, and is modified by, many small and large molecules. Therefore, the focus of the present study was to address the impact of specific known biological albumin modifications on albumin-FcRn binding and cellular handling. Binding at pH 6.0 and 7.4 was performed since FcRn binds albumin strongly at acidic pH and releases it after transcytosis at physiological pH. Equilibrium dissociation constants were measured using microscale thermophoresis. Since studies have shown that glycated albumin is excreted in the urine at a higher rate than unmodified albumin, we studied glucose and methylgloxal modified albumins (21 days). All had reduced affinity to FcRn at pH 6.0, suggesting these albumins would not be returned to the circulation via the transcytotic pathway. To address why modified albumin has reduced affinity, we analyzed the structure of the modified albumins using small-angle X-ray scattering. This analysis showed significant structural changes occurring to albumin with glycation, particularly in the FcRn-binding region, which could explain the reduced affinity to FcRn. These results offer an explanation for enhanced proximal tubule-mediated sorting and clearance of abnormal albumins.

Indexed as

AnimalsCHO CellsCricetinaeCricetulusGlycated Serum AlbuminGlycation End Products, AdvancedHistocompatibility Antigens Class IHumansImmunoglobulin GKidney GlomerulusKidney Tubules, ProximalMaleRatsRats, Sprague-DawleyReceptors, FcScattering, Small AngleFc receptor, neonatalGlycated Serum AlbuminGlycation End Products, AdvancedHistocompatibility Antigens Class IImmunoglobulin GReceptors, FcSerum Albuminalbuminuriacell biology and structurediabetesglycationneonatal Fc receptorproximal tubule

Identifiers

PMID26887834
PMCPMC4889321
OpenAlexW2275278202

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.