Evidence map›Paper›PMID 41111488›Full record

ArticleJournal of biomedical optics2025

Multimodal microscope for optical coherence microscopy, tomography, vibrometry, and two-photon microscopy in the living mouse cochlea.

Clayton B Walker, Michael J Serafino, Patricia M Quiñones, James B Dewey, John S Oghalai, Brian E Applegate

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Clayton B WalkerTexas A&M University, Department of Biomedical Engineering, College Station, Texas, United States.ORCID https://orcid.org/0000-0003-1137-9071
Michael J SerafinoUniversity of Southern California, Keck School of Medicine, Caruso Department of Otolaryngology - Head and Neck Surgery, Los Angeles, California, United States.
Patricia M QuiñonesUniversity of Southern California, Keck School of Medicine, Caruso Department of Otolaryngology - Head and Neck Surgery, Los Angeles, California, United States.
James B DeweyUniversity of Southern California, Keck School of Medicine, Caruso Department of Otolaryngology - Head and Neck Surgery, Los Angeles, California, United States.ORCID https://orcid.org/0000-0001-5715-9125
John S OghalaiUniversity of Southern California, Keck School of Medicine, Caruso Department of Otolaryngology - Head and Neck Surgery, Los Angeles, California, United States.ORCID https://orcid.org/0000-0003-4241-6189
Brian E ApplegateUniversity of Southern California, Keck School of Medicine, Caruso Department of Otolaryngology - Head and Neck Surgery, Los Angeles, California, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Our understanding of mechanotransduction in mammalian inner ears remains incomplete, in part due to imaging limitations: current systems cannot simultaneously provide high-resolution images needed for subcellular analysis and the deep focus required for structural mechanics. Optical coherence tomography (OCT) enables structural and vibrational imaging through the bone of the intact cochlea in models such as mice, supporting studies of cochlear mechanics in animals with functional hearing. However, capturing both cellular ( Aim: We aim to develop an integrated OCT and two-photon microscope optimized for imaging the morphology and function of the cochlea. Approach: We integrated a custom SD-OCT/TPM system into an upright microscope with a high-precision stage for animal positioning. The system uses two tunable liquid lenses to form a beam expander, enabling dynamic adjustment of the beam diameter at the back aperture of each objective. This optimized light throughput and maintained a high signal-to-noise ratio (SNR) across all objectives. In addition, we automated optical adjustments to facilitate seamless imaging with a wide range of objectives. Results: For each objective, we measured the SNR difference between a beam expanded to match the largest back aperture and a beam adjusted to match the back aperture of the objective. Except for the Conclusions: Automation and optimization of the optical system enabled seamless multiscale imaging of the murine cochlea, providing high-quality morphological, functional, and two-photon fluorescence images. The dynamic adjustment of the beam diameter within the microscope was essential for maintaining high SNR across a wide range of numerical apertures.

Indexed as

CochleaMicroscopy, Fluorescence, MultiphotonMultimodal ImagingTomography, Optical CoherenceAnimalsEquipment DesignMiceMice, Inbred C57BLVibrationbiophotonicsmicroscopyoptical coherence microscopyoptical coherence tomography

Identifiers

PMID41111488
PMCPMC12529084

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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.