Evidence map›Paper›PMID 32764142›Full record

ArticleJournal of the American Society of Nephrology : JASN2020

Apolipoprotein L1-Specific Antibodies Detect Endogenous APOL1 inside the Endoplasmic Reticulum and on the Plasma Membrane of Podocytes.

Suzie J Scales, Nidhi Gupta, Ann M De Mazière, George Posthuma, Cecilia P Chiu, Andrew A Pierce, Kathy Hötzel, Jianhua Tao, Oded Foreman, Georgios Koukos and 4 more

Open access · bronzeAbstract 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 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. A novelRenal failure · 2025
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  7. Article
  8. Article
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  14. Article
  15. Preeclampsia in mice carrying fetuses with APOL1 risk variants.bioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Novel Therapies inKidney international reports · 2023
    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

14 authors at 1 institution in 1 country.

Suzie J ScalesDepartment of Molecular Biology, Genentech, South San Francisco, California sscales@gene.com.ORCID 0000-0003-2544-0283
Nidhi GuptaDepartment of Molecular Biology, Genentech, South San Francisco, California.
Ann M De MazièreSection of Cell Biology, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
George PosthumaSection of Cell Biology, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Cecilia P ChiuDepartment of Antibody Engineering, Genentech, South San Francisco, California.
Andrew A PierceDepartment of Pathology, Genentech, South San Francisco, California.
Kathy HötzelDepartment of Pathology, Genentech, South San Francisco, California.
Jianhua TaoDepartment of Pathology, Genentech, South San Francisco, California.
Oded ForemanDepartment of Pathology, Genentech, South San Francisco, California.
Georgios KoukosDepartment of Molecular Biology, Genentech, South San Francisco, California.
Francesca OltrabellaDepartment of Molecular Biology, Genentech, South San Francisco, California.
Judith KlumpermanSection of Cell Biology, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
WeiYu LinDepartment of Antibody Engineering, Genentech, South San Francisco, California.
Andrew S PetersonDepartment of Molecular Biology, Genentech, South San Francisco, California.
Utrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAPOL1 is found in human kidney podocytes and endothelia. Variants G1 and G2 of the

methodsImmunohistochemistry, confocal and immunoelectron microscopy, and podocyte fractionation localized endogenous and transfected APOL1 using a large panel of novel APOL1-specific mouse and rabbit monoclonal antibodies.

resultsBoth endogenous podocyte and transfected APOL1 isoforms vA and vB1 (and a little of isoform vC) localize to the luminal face of the endoplasmic reticulum (ER) and to the cell surface, but not to mitochondria, endosomes, or lipid droplets. In contrast, APOL2, isoform vB3, and most vC of APOL1 localize to the cytoplasmic face of the ER and are consequently absent from the cell surface.

conclusionsAPOL1 is found in the ER and plasma membrane, consistent with either the ER stress or surface cation channel models of APOL1-mediated cytotoxicity. The surface localization of APOL1 variants potentially opens new therapeutic targeting avenues.

Indexed as

AnimalsAntibodiesApolipoprotein L1Apolipoproteins LCell MembraneCells, CulturedChlorocebus aethiopsCOS CellsCross ReactionsEndoplasmic ReticulumHumansImmunohistochemistryMiceMice, Inbred C57BLPodocytesAntibodiesAPOL2 protein, humanApolipoprotein L1Apolipoproteins LApolipoprotein L1Apolipoprotein L2chronic kidney diseaseimmunofluorescenceimmunohistochemistrypodocyte

Identifiers

PMID32764142
PMCPMC7461670
OpenAlexW3047928811

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.