Evidence map›Paper›PMID 27339387›Full record

ReviewSeminars in nephrology2016

Just Look! Intravital Microscopy as the Best Means to Study Kidney Cell Death Dynamics.

Ina Maria Schießl, Anna Hammer, Anne Riquier-Brison, Janos Peti-Peterdi

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in nephrology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Actually Seeing What Is Going on - Intravital Microscopy in Tissue Engineering.Frontiers in bioengineering and biotechnology · 2021
    Review
  6. Article
  7. Review
  8. Advances in Renal Cell Imaging.Seminars in nephrology · 2018
    Review
  9. 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

4 authors at 2 institutions in 2 countries.

Ina Maria SchießlInstitute of Physiology, University of Regensburg, Regensburg, Germany. Electronic address: Ina.schiessl@vkl.uni-regensburg.de.
Anna HammerInstitute of Physiology, University of Regensburg, Regensburg, Germany.
Anne Riquier-BrisonDepartment of Physiology and Biophysics, Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, CA.
Janos Peti-PeterdiDepartment of Physiology and Biophysics, Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, CA.
University of Regensburg · DEUniversity of Southern California · US

Funding

Multiphoton Imaging of the Juxtaglomerular ApparatusR01DK064324 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2004 to 2026
$8.4M
Novel imaging approach to study podocyte function in vivoR01DK100944 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PETI-PETERDI, JANOS · 2014 to 2017
$1.5M
NIDDK NIH HHS R01 DK064324NIDDK NIH HHS R01 DK100944
6 · The paper itself

Abstract

Kidney cell death plays a key role in the progression of life-threatening renal diseases, such as acute kidney injury and chronic kidney disease. Injured and dying epithelial and endothelial cells take part in complex communication with the innate immune system, which drives the progression of cell death and the decrease in renal function. To improve our understanding of kidney cell death dynamics and its impact on renal disease, a study approach is needed that facilitates the visualization of renal function and morphology in real time. Intravital multiphoton microscopy of the kidney has been used for more than a decade and made substantial contributions to our understanding of kidney physiology and pathophysiology. It is a unique tool that relates renal structure and function in a time- and spatial-dependent manner. Basic renal function, such as microvascular blood flow regulation and glomerular filtration, can be determined in real time and homeostatic alterations, which are linked inevitably to cell death and can be depicted down to the subcellular level. This review provides an overview of the available techniques to study kidney dysfunction and inflammation in terms of cell death in vivo, and addresses how this novel approach can be used to improve our understanding of cell death dynamics in renal disease.

Indexed as

Cell DeathAcute Kidney InjuryCell AdhesionEndothelial CellsHumansIntravital MicroscopyKidneyKidney Tubules, ProximalLeukocyte RollingLeukocytesMicroscopy, Fluorescence, MultiphotonRenal Insufficiency, Chronicacute kidney injurychronic kidney diseaseIntravital multiphoton microscopyregulated cell deathrenal dysfunction

Identifiers

PMID27339387
PMCPMC5425152
OpenAlexW2475137746

What OpenQuestion holds

Textmetadata
LicenceTDM
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.