Evidence map›Paper›PMID 32766264›Full record

ArticleFrontiers in medicine2020

From 2D to 3D: Promising Advances in Imaging Lung Structure.

Timothy Klouda, David Condon, Yuan Hao, Wen Tian, Maria Lvova, Ananya Chakraborty, Mark R Nicolls, Xiaobo Zhou, Benjamin A Raby, Ke Yuan

Abstract read
In one paragraph

Article in Frontiers in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Multiresolution 3D Optical Mapping of Immune Cell Infiltrates in Mouse Asthmatic Lung.American journal of respiratory cell and molecular biology · 2023
    Article
  8. 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

10 authors.

Timothy KloudaDivisions of Pulmonary Medicine, Boston Children's Hospital, Boston, MA, United States.
David CondonDivision of Pulmonary, Allery and Critical Care Medicine, Stanford University, Stanford, CA, United States.
Yuan HaoDivisions of Pulmonary Medicine, Boston Children's Hospital, Boston, MA, United States.
Wen TianDivision of Pulmonary, Allery and Critical Care Medicine, Stanford University, Stanford, CA, United States.
Maria LvovaDivisions of Pulmonary Medicine, Boston Children's Hospital, Boston, MA, United States.
Ananya ChakrabortyDivision of Pulmonary, Allery and Critical Care Medicine, Stanford University, Stanford, CA, United States.
Mark R NicollsDivision of Pulmonary, Allery and Critical Care Medicine, Stanford University, Stanford, CA, United States.
Xiaobo ZhouDivision of Pulmonary and Critical Care Medicine, Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Benjamin A RabyDivisions of Pulmonary Medicine, Boston Children's Hospital, Boston, MA, United States.
Ke YuanDivisions of Pulmonary Medicine, Boston Children's Hospital, Boston, MA, United States.

Funding

Super-Resolution ImagingP30NS072030 · NINDS · HARVARD MEDICAL SCHOOL · PI REGEHR, WADE G · 2011 to 2020
$5.8M
Endothelial Injury, BMPR2 Dysfunction and Macrophage Activation Cause EndMT and PAHR01HL138473 · NHLBI · STANFORD UNIVERSITY · PI Mark Robert Nicolls, Marlene Rabinovitch · 2017 to 2026
$4.9M
Critical Role for Microvasculature in Airway TransplantationR01HL095686 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI NICOLLS, MARK ROBERT · 2010 to 2022
$4.7M
A Critical Role for Leukotriene B4 in LymphedemaR01HL141105 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI NICOLLS, MARK ROBERT · 2019 to 2022
$2.3M
NHLBI NIH HHS R01 HL095686NHLBI NIH HHS R01 HL141105NINDS NIH HHS P30 NS072030
6 · The paper itself

Abstract

The delicate structure of murine lungs poses many challenges for acquiring high-quality images that truly represent the living lung. Here, we describe several optimized procedures for obtaining and imaging murine lung tissue. Compared to traditional paraffin cross-section and optimal cutting temperature (OCT), agarose-inflated vibratome sections (aka precision-cut lung slices), combines comparable structural preservation with experimental flexibility. In particular, we discuss an optimized procedure to precision-cut lung slices that can be used to visualize three-dimensional cell-cell interactions beyond the limitations of two-dimensional imaging. Super-resolution microscopy can then be used to reveal the fine structure of lung tissue's cellular bodies and processes that regular confocal cannot. Lastly, we evaluate the entire lung vasculature with clearing technology that allows imaging of the entire volume of the lung without sectioning. In this manuscript, we combine the above procedures to create a novel and evolutionary method to study cell behavior

Indexed as

confocallung structureoptical clearingprecision cut lung slicesSTEDvibratome

Identifiers

PMID32766264
PMCPMC7381109

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.