Evidence map›Paper›PMID 27836988›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2017

Sphingomyelinase-like phosphodiesterase 3b mediates radiation-induced damage of renal podocytes.

Anis Ahmad, Alla Mitrofanova, Jacek Bielawski, Yidong Yang, Brian Marples, Alessia Fornoni, Youssef H Zeidan

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

42 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Sphingolipid signaling in kidney diseases.American journal of physiology. Renal physiology · 2025
    Review
  8. Article
  9. Article
  10. Sphingolipids and Chronic Kidney Disease.Journal of clinical medicine · 2024
    Review
  11. Review
  12. Article
  13. Review
  14. Radiation nephropathy: Mechanisms of injury and recovery in a murine model.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. SMPDL3b modulates radiation-induced DNA damage response in renal podocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  19. The Perspective of Vitamin D on suPAR-Related AKI in COVID-19.International journal of molecular sciences · 2022
    Review
  20. 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

7 authors at 5 institutions in 3 countries.

Anis AhmadDepartment of Radiation Oncology, Miller School of Medicine/Sylvester Cancer Center, University of Miami, Miami, Florida, USA.
Alla MitrofanovaPeggy and Harold Katz Family Drug Discovery Center, University of Miami, Miami, Florida, USA.
Jacek BielawskiDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina, USA.
Yidong YangDepartment of Radiation Oncology, Miller School of Medicine/Sylvester Cancer Center, University of Miami, Miami, Florida, USA.
Brian MarplesDepartment of Radiation Oncology, Miller School of Medicine/Sylvester Cancer Center, University of Miami, Miami, Florida, USA.
Alessia FornoniPeggy and Harold Katz Family Drug Discovery Center, University of Miami, Miami, Florida, USA.
Youssef H ZeidanDepartment of Radiation Oncology, Miller School of Medicine/Sylvester Cancer Center, University of Miami, Miami, Florida, USA; yz09@aub.edu.lb.
University of Miami · USAmerican University of Beirut · LBMedical University of South Carolina · USSylvester Comprehensive Cancer Center · USUniversity of Miami Hospital · US

Funding

Miami Clinical and Translational Science InstituteUL1TR000460 · NCATS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SACCO, RALPH L. · 2012 to 2016
$16.9M
Crosstalk Between Lipid Droplets and Other Organelles in PodocytesR01DK104753 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FORNONI, ALESSIA · 2015 to 2025
$5.9M
Novel Targets of Rituximab in FSGSR01DK090316 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FORNONI, ALESSIA · 2011 to 2015
$1.7M
Crosstalk between lipid droplets and other organelles in podocytesR56DK104753 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FORNONI, ALESSIA · 2023 to 2023
$100k
NCATS NIH HHS UL1 TR000460NIDDK NIH HHS R01 DK090316NIDDK NIH HHS R01 DK104753NIDDK NIH HHS R56 DK104753
6 · The paper itself

Abstract

The molecular mechanisms responsible for the development of proteinuria and glomerulosclerosis in radiation nephropathy remain largely unknown. Podocytes are increasingly recognized as key players in the pathogenesis of proteinuria in primary and secondary glomerular disorders. The lipid-modulating enzyme sphingomyelin phosphodiesterase acid-like 3B (SMPDL3b) is a key determinant of podocyte injury and a known off target of the anti-CD20 antibody rituximab (RTX). The current study investigates the role of sphingolipids in radiation-induced podocytopathy. After a single dose of radiation (8 Gy), several ceramide species were significantly elevated. In particular, C16:00, C24:00, and C24:1 ceramides were the most abundant ceramide species detected. These changes were paralleled by a time-dependent drop in SMPDL3b protein, sphingosine, and sphingosine-1-phosphate levels. Interestingly, SMPDL3b-overexpressing podocytes had higher basal levels of sphingosine-1-phosphate and maintained basal ceramide levels after irradiation. Morphologically, irradiated podocytes demonstrated loss of filopodia and remodeling of cortical actin. Furthermore, the actin binding protein ezrin relocated from the plasma membrane to the cytosol as early as 2 h after radiation. In contrast, SMPDL3b overexpressing podocytes were protected from radiation-induced cytoskeletal remodeling. Treatment with RTX before radiation exposure partially protected podocytes from SMPDL3b loss, cytoskeletal remodeling, and caspase 3 cleavage. Our results demonstrate that radiation injury induces early cytoskeletal remodeling, down-regulation of SMPDL3b, and elevation of cellular ceramide levels. Overexpression of SMPDL3b and pretreatment with RTX confer a radioprotective effect in cultured podocytes. These findings indicate a potential role for SMPDL3b and RTX in radiation-induced podocytopathy.-Ahmad, A., Mitrofanova, A., Bielawski, J., Yang, Y., Marples, B., Fornoni, A., Zeidan, Y. H. Sphingomyelinase-like phosphodiesterase 3b mediates radiation-induced damage of renal podocytes.

Indexed as

AnimalsCeramidesCyclic Nucleotide Phosphodiesterases, Type 3Down-RegulationGene Expression Regulation, EnzymologicHumansImmunologic FactorsMiceMice, Inbred C57BLPodocytesRituximabSphingomyelin PhosphodiesteraseCeramidesCyclic Nucleotide Phosphodiesterases, Type 3Immunologic FactorsRituximabSMPDL3B protein, humansphingomyelinase-like phosphodiesterase 3b, mouseSphingomyelin Phosphodiesterasecancerceramidelipidsradioprotection

Identifiers

PMID27836988
PMCPMC6137603
OpenAlexW2551956856

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.