Evidence map›Paper›PMID 28916834›Full record

ArticleScientific reports2017

Ultrastructural Characterization of the Glomerulopathy in Alport Mice by Helium Ion Scanning Microscopy (HIM).

Kenji Tsuji, Hani Suleiman, Jeffrey H Miner, James M Daley, Diane E Capen, Teodor G Păunescu, Hua A Jenny Lu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Identification of an Altered Matrix Signature in Kidney Aging and Disease.Journal of the American Society of Nephrology : JASN · 2021
    Article
  5. Complexities of the glomerular basement membrane.Nature reviews. Nephrology · 2021
    Review
  6. Article
  7. Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.Matrix biology : journal of the International Society for Matrix Biology · 2018
    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

7 authors at 5 institutions in 1 country.

Kenji TsujiCenter for Systems Biology, Program in Membrane Biology and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA.
Hani SuleimanDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.
Jeffrey H MinerDivision of Nephrology, Washington University School of Medicine, St. Louis, MO, USA.
James M DaleyResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA, USA.
Diane E CapenCenter for Systems Biology, Program in Membrane Biology and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA.
Teodor G PăunescuCenter for Systems Biology, Program in Membrane Biology and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA.
Hua A Jenny LuCenter for Systems Biology, Program in Membrane Biology and Division of Nephrology, Department of Medicine, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA. halu@partners.org.
Massachusetts General Hospital · USWashington University in St. Louis · USCenter for Systems Biology · USHarvard University · USMassachusetts Institute of Technology · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BROWN, DENNIS · 2000 to 2019
$31.4M
STRUCTURE AND FUNCTION OF CD2AP IN THE KIDNEYR01DK058366 · NIDDK · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H · 2000 to 2019
$6.8M
LAMININS AND GLOMERULAR FILTRATIONR01DK078314 · NIDDK · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H · 2008 to 2021
$5.4M
Novel roles of integrin b1 signaling in regulating principal cell function andmaintaining collecting duct integrityR01DK096015 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LU, HUA A · 2013 to 2022
$3.7M
PATHOGENESIS OF ALPORT SYNDROMER56DK100593 · NIDDK · WASHINGTON UNIVERSITY · PI JARAD, GEORGE, MINER, JEFFREY H · 2014 to 2015
$458k
Role of the novel gene fam4b in phosphatidylserine synthesis in podocytes and maiR21DK092619 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LU, HUA A · 2012 to 2012
$257k
NIDDK NIH HHS P30 DK043351NIDDK NIH HHS P30 DK057521NIDDK NIH HHS R01 DK058366NIDDK NIH HHS R01 DK078314NIDDK NIH HHS R01 DK096015NIDDK NIH HHS R21 DK092619NIDDK NIH HHS R56 DK100593
6 · The paper itself

Abstract

The glomerulus exercises its filtration barrier function by establishing a complex filtration apparatus consisting of podocyte foot processes, glomerular basement membrane and endothelial cells. Disruption of any component of the glomerular filtration barrier leads to glomerular dysfunction, frequently manifested as proteinuria. Ultrastructural studies of the glomerulus by transmission electron microscopy (TEM) and conventional scanning electron microscopy (SEM) have been routinely used to identify and classify various glomerular diseases. Here we report the application of newly developed helium ion scanning microscopy (HIM) to examine the glomerulopathy in a Col4a3 mutant/Alport syndrome mouse model. Our study revealed unprecedented details of glomerular abnormalities in Col4a3 mutants including distorted podocyte cell bodies and disorganized primary processes. Strikingly, we observed abundant filamentous microprojections arising from podocyte cell bodies and processes, and presence of unique bridging processes that connect the primary processes and foot processes in Alport mice. Furthermore, we detected an altered glomerular endothelium with disrupted sub-endothelial integrity. More importantly, we were able to clearly visualize the complex, three-dimensional podocyte and endothelial interface by HIM. Our study demonstrates that HIM provides nanometer resolution to uncover and rediscover critical ultrastructural characteristics of the glomerulopathy in Col4a3 mutant mice.

Indexed as

AnimalsAutoantigensCollagen Type IVEndothelial CellsGlomerulonephritisKidney GlomerulusLasers, GasMiceMice, Mutant StrainsMicroscopy, ConfocalPodocytesAutoantigensCollagen Type IVtype IV collagen alpha3 chain

Identifiers

PMID28916834
PMCPMC5601433
OpenAlexW2755568622

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.