Evidence map›Paper›PMID 28911733›Full record

ArticleMethods (San Diego, Calif.)2017

Time-lapsed, large-volume, high-resolution intravital imaging for tissue-wide analysis of single cell dynamics.

David Entenberg, Jessica M Pastoriza, Maja H Oktay, Sonia Voiculescu, Yarong Wang, Maria Soledad Sosa, Julio Aguirre-Ghiso, John Condeelis

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Imaging Approaches in Cancer Biology.Cold Spring Harbor perspectives in medicine · 2024
    Review
  4. Article
  5. Review
  6. Stabilized Window for Intravital Imaging of the Murine Pancreas.Journal of visualized experiments : JoVE · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Science translational medicine · 2022
    Article
  12. Review
  13. Multiphoton intravital microscopy of rodents.Nature reviews. Methods primers · 2022
    Article
  14. Article
  15. A Permanent Window for Investigating Cancer Metastasis to the Lung.Journal of visualized experiments : JoVE · 2021
    Article
  16. Article
  17. The Indiana O'Brien Center for Advanced Renal Microscopic Analysis.American journal of physiology. Renal physiology · 2021
    Review
  18. Article
  19. The Cellular Organization of the Mammary Gland: Insights From Microscopy.Journal of mammary gland biology and neoplasia · 2021
    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

8 authors at 2 institutions in 1 country.

David EntenbergAnatomy and Structural Biology, Integrated Imaging Program, Gruss-Lipper Biophotonics Center, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States. Electronic address: david.entenberg@einstein.yu.edu.
Jessica M PastorizaDepartment of Surgery, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States.
Maja H OktayAnatomy and Structural Biology, Integrated Imaging Program, Gruss-Lipper Biophotonics Center, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States; Department of Pathology, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States.
Sonia VoiculescuDepartment of Surgery, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States.
Yarong WangAnatomy and Structural Biology, Integrated Imaging Program, Gruss-Lipper Biophotonics Center, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States.
Maria Soledad SosaDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Julio Aguirre-GhisoDivision of Hematology and Oncology, Department of Medicine, Department of Otolaryngology, Department of Oncological Sciences, Tisch Cancer Institute, Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
John CondeelisAnatomy and Structural Biology, Integrated Imaging Program, Gruss-Lipper Biophotonics Center, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States.
Montefiore Medical Center · USIcahn School of Medicine at Mount Sinai · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Tumor Progression and MetastasisP01CA100324 · NCI · YESHIVA UNIVERSITY · PI CONDEELIS, JOHN S · 2003 to 2018
$30.0M
Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
Tumor microenvironments determing migration, dissemination and dormancyU54CA163131 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AGUIRRE-GHISO, JULIO A., CASTRACANE, JAMES · 2011 to 2015
$3.9M
(7) Novel imaging devices for measurement and control of tumor microenvironmentsR01CA216248 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CADY, NATHANIEL CHARLES, CONDEELIS, JOHN S · 2017 to 2021
$2.9M
Training of Surgeons for Studies of the Tumor MicroenvironmentT32CA200561 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MCAULIFFE, JOHN · 2015 to 2024
$2.7M
NCI NIH HHS P01 CA100324NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA109182NCI NIH HHS R01 CA216248NCI NIH HHS T32 CA200561NCI NIH HHS U54 CA163131
6 · The paper itself

Abstract

Pathologists rely on microscopy to diagnose disease states in tissues and organs. They utilize both high-resolution, high-magnification images to interpret the staining and morphology of individual cells, as well as low-magnification overviews to give context and location to these cells. Intravital imaging is a powerful technique for studying cells and tissues in their native, live environment and can yield sub-cellular resolution images similar to those used by pathologists. However, technical limitations prevent the straightforward acquisition of low-magnification images during intravital imaging, and they are hence not typically captured. The serial acquisition, mosaicking, and stitching together of many high-resolution, high-magnification fields of view is a technique that overcomes these limitations in fixed and ex vivo tissues. The technique however, has not to date been widely applied to intravital imaging as movements caused by the living animal induce image distortions that are difficult to compensate for computationally. To address this, we have developed techniques for the stabilization of numerous tissues, including extremely compliant tissues, that have traditionally been extremely difficult to image. We present a novel combination of these stabilization techniques with mosaicked and stitched intravital imaging, resulting in a process we call Large-Volume High-Resolution Intravital Imaging (LVHR-IVI). The techniques we present are validated and make large volume intravital imaging accessible to any lab with a multiphoton microscope.

Indexed as

Fluorescent DyesAnimalsCell MovementIntravital MicroscopyMiceMice, Inbred C57BLMicroscopy, Fluorescence, MultiphotonPericardial Window TechniquesSingle-Cell AnalysisTime-Lapse ImagingFluorescent DyesIntravital imagingMosaicMulti-scale imagingStitching

Identifiers

PMID28911733
PMCPMC5659295
OpenAlexW2755199335

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.