Evidence map›Paper›PMID 36912542›Full record

ArticleJournal of visualized experiments : JoVE2023

A Fluorescent Intravital Imaging Approach to Study Load-Induced Calcium Signaling Dynamics in Mouse Osteocytes.

Karl J Lewis, James F Boorman-Padgett, Macy Castaneda, David C Spray, Mia M Thi, Mitchell B Schaffler

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Karl J LewisMeinig School of Biomedical Engineering, Cornell University; kjl235@cornell.edu.
James F Boorman-PadgettDepartment of Biomedical Engineering, The City College of New York.
Macy CastanedaSibley School of Mechanical and Aerospace Engineering, Cornell University.
David C SprayDepartment of Neuroscience, Albert Einstein College of Medicine.
Mia M ThiDepartment of Orthopaedic Surgery, Albert Einstein College of Medicine; Department of Molecular Pharmacology, Albert Einstein College of Medicine.
Mitchell B SchafflerDepartment of Biomedical Engineering, The City College of New York.
Albert Einstein College of Medicine · USCity College of New York · USCornell University · US

Funding

Osteocyte Integrity and Bone RemodelingR01AR041210 · NIAMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHAFFLER, MITCHELL B · 1997 to 2019
$5.8M
Structural, Molecular and Functional Specialization in Osteocyte MechanosensingR01AR070547 · NIAMS · CITY COLLEGE OF NEW YORK · PI SCHAFFLER, MITCHELL B, SPRAY, DAVID C · 2018 to 2022
$3.2M
Structural, Molecular, and Functional Specialization in Osteocyte MechanosensingR01AR057139 · NIAMS · CITY COLLEGE OF NEW YORK · PI SCHAFFLER, MITCHELL B, SPRAY, DAVID C · 2010 to 2014
$2.5M
NIAMS NIH HHS R01 AR041210NIAMS NIH HHS R01 AR057139NIAMS NIH HHS R01 AR070547
6 · The paper itself

Abstract

Bone tissue is exquisitely sensitive to differences in mechanical load magnitude. Osteocytes, dendritic cells that form a syncytium throughout the bone, are responsible for the mechanosensory function of bone tissue. Studies employing histology, mathematical modeling, cell culture, and ex vivo bone organ cultures have greatly advanced the understanding of osteocyte mechanobiology. However, the fundamental question of how osteocytes respond to and encode mechanical information at the molecular level in vivo is not well understood. Intracellular calcium concentration fluctuations in osteocytes offer a useful target for learning more about acute bone mechanotransduction mechanisms. Here, we report a method for studying osteocyte mechanobiology in vivo, combining a mouse strain with a fluorescently genetically encoded calcium indicator expressed in osteocytes with an in vivo loading and imaging system to directly detect osteocyte calcium levels during loading. This is achieved with a three-point bending device that can deliver well-defined mechanical loads to the third metatarsal of living mice while simultaneously monitoring fluorescently indicated calcium responses of osteocytes using two-photon microscopy. This technique allows for direct in vivo observation of osteocyte calcium signaling events in response to whole bone loading and is useful in the endeavor to reveal mechanisms in osteocyte mechanobiology.

Indexed as

Mechanotransduction, CellularOsteocytesAnimalsCalciumCalcium SignalingColoring AgentsIntravital MicroscopyMiceStress, MechanicalCalciumColoring Agents

Identifiers

PMID36912542
PMCPMC13536361
OpenAlexW4321763857

What OpenQuestion holds

Textmetadata
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.