Evidence map›Paper›PMID 31087287›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2020

Long-Term Cell Fate Tracking of Individual Renal Cells Using Serial Intravital Microscopy.

Ina Maria Schiessl, Katharina Fremter, James L Burford, Hayo Castrop, Janos Peti-Peterdi

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
10.1field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

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  17. A new view of macula densa cell microanatomy.American journal of physiology. Renal physiology · 2021
    Article
  18. Review
  19. Intravital Imaging Allows Organ-Specific Insights Into Immune Functions.Frontiers in cell and developmental biology · 2021
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Ina Maria SchiesslDepartment of Physiology and Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. Ina.maria.schiessl@gmail.com.
Katharina FremterInstitute of Physiology, University of Regensburg, Regensburg, Germany.
James L BurfordDepartment of Ophthalmology, University of Southern California, Los Angeles, CA, USA.
Hayo CastropInstitute of Physiology, University of Regensburg, Regensburg, Germany.
Janos Peti-PeterdiDepartment of Physiology and Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
University of Southern California · USUniversity of Regensburg · DE

Funding

Multiphoton Imaging of the Juxtaglomerular ApparatusR01DK064324 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2004 to 2026
$8.4M
Novel regulatory mechanisms of the glomerular endotheliumR01DK123564 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2019 to 2026
$3.5M
Multiphoton microscope replacement for USC shared resourceS10OD021833 · OD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PETI-PETERDI, JANOS · 2017 to 2017
$600k
NIDDK NIH HHS R01 DK064324NIDDK NIH HHS R01 DK123564NIH HHS S10 OD021833
6 · The paper itself

Abstract

Intravital multiphoton microscopy of the kidney is a powerful technique to study alterations in tissue morphology and function simultaneously in the living animal and represents a dynamic and developing research tool in the field. Recent technological advances include serial intravital multiphoton microscopy of the same kidney regions over several weeks and combined with ex vivo histology for cellular biomarker expression of the same cells, which had been subject to serial imaging before. Thus, serial intravital multiphoton microscopy followed by ex vivo histology provides unique tools to perform long-term cell fate tracing of the same renal cells during physiological and pathophysiological conditions, thereby allowing the detection of structural changes of the same renal cells over time. Examples include renal cell migration and proliferation while linking these events to local functional alterations and eventually to the expression of distinct cellular biomarkers. Here, we provide a detailed step-by-step protocol to facilitate serial intravital multiphoton microscopy for long-term in vivo tracking of renal cells and subsequent ex vivo histology for immunohistological staining of the same cells in the fixed tissue.

Indexed as

AbdomenAnimalsCell TrackingFluorescent DyesInjectionsIntravital MicroscopyKidneyMiceFluorescent DyesCell fate trackingFluorescent reporterImmunohistologyIntravital imagingMultiphoton microscopyTissue remodeling

Identifiers

PMID31087287
PMCPMC6854295
OpenAlexW2949780954

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.