Evidence map›Paper›PMID 31360606›Full record

ArticleBiomedical optics express2019

Five-dimensional two-photon volumetric microscopy of in-vivo dynamic activities using liquid lens remote focusing.

Kayvan Forouhesh Tehrani, Charles V Latchoumane, W Michael Southern, Emily G Pendleton, Ana Maslesa, Lohitash Karumbaiah, Jarrod A Call, Luke J Mortensen

Abstract read
In one paragraph

Article in Biomedical optics express, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
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  5. Recent advances in oblique plane microscopy.Nanophotonics (Berlin, Germany) · 2023
    Review
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  19. Nonlinear Imaging Histopathology: A Pipeline to Correlate Gold-Standard Hematoxylin and Eosin Staining With Modern Nonlinear Microscopy.IEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society
    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.

Kayvan Forouhesh TehraniRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Charles V LatchoumaneRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
W Michael SouthernDepartment of Kinesiology, University of Georgia, Athens, GA 30602, USA.
Emily G PendletonRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Ana MaslesaRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Lohitash KarumbaiahRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Jarrod A CallRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Luke J MortensenRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.

Funding

TRAINING PROGRAM IN MUSCLE RESEARCHT32AR007612 · NIAMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JAMES M ERVASTI, DAWN A LOWE · 2001 to 2026
$11.3M
Super resolution label-free imaging in highly scattering boneR21EB027802 · NIBIB · UNIVERSITY OF GEORGIA · PI MORTENSEN, LUKE J. · 2019 to 2021
$568k
NIAMS NIH HHS T32 AR007612NIBIB NIH HHS R21 EB027802
6 · The paper itself

Abstract

Multi-photon scanning microscopy provides a robust tool for optical sectioning, which can be used to capture fast biological events such as blood flow, mitochondrial activity, and neuronal action potentials. For many studies, it is important to visualize several different focal planes at a rate akin to the biological event frequency. Typically, a microscope is equipped with mechanical elements to move either the sample or the objective lens to capture volumetric information, but these strategies are limited due to their slow speeds or inertial artifacts. To overcome this problem, remote focusing methods have been developed to shift the focal plane axially without physical movement of the sample or the microscope. Among these methods is liquid lens technology, which adjusts the focus of the lens by changing the wettability of the liquid and hence its curvature. Liquid lenses are inexpensive active optical elements that have the potential for fast multi-photon volumetric imaging, hence a promising and accessible approach for the study of biological systems with complex dynamics. Although remote focusing using liquid lens technology can be used for volumetric point scanning multi-photon microscopy, optical aberrations and the effects of high energy laser pulses have been concerns in its implementation. In this paper, we characterize a liquid lens and validate its use in relevant biological applications. We measured optical aberrations that are caused by the liquid lens, and calculated its response time, defocus hysteresis, and thermal response to a pulsed laser. We applied this method of remote focusing for imaging and measurement of multiple in-vivo specimens, including mesenchymal stem cell dynamics, mouse tibialis anterior muscle mitochondrial electrical potential fluctuations, and mouse brain neural activity. Our system produces 5 dimensional (x,y,z,λ,t) data sets at the speed of 4.2 volumes per second over volumes as large as 160 x 160 x 35 µm

Identifiers

PMID31360606
PMCPMC6640832

What OpenQuestion holds

Textmetadata
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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.