Name: A Fluorescent Intravital Imaging Approach to Study Load-Induced Calcium Signaling Dynamics in Mouse Osteocytes (Video) | JoVE Journal
Uploaded: 2023-02-24T14:05:00.000+00:00
Duration: 5 min 3 s
Description: Discover intravital imaging techniques to study calcium signaling dynamics in mouse osteocytes during mechanical loading. This method enables real-time observation of cellular responses in their native bone environment.

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5 minutes

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All methods have been approved by the Institutional Animal Care and Use Committee (IACUC) at Cornell University.
1. Preparation of materials and equipment
<ol>
	<li>Design and build the metatarsal loading device for use with an overhead multiphoton microscope. 
	NOTE: Details for component specifications and device operation are described in the supplementary documentation of a previous study25. Briefly, the major components consist of an actuator in series with a load cell and loading bracket, a water bath, and a fulcrum pin. The actuator and load cell can be obtained commercially and should be capable of accommodating loads up to 300 g. The water bath, fulcrum pin, and load bracket should be constructed of titanium or stainless steel. They can be fabricated in-house or commercially via 3D metal printing.</li>
	<li>Calibrate the strain magnitude values to the actuator displacement in advance for individual mouse groups (i.e., sex, treatment, genotype). This is done using surface strain mapping in a procedure outlined in a previous study25.</li>
	<li>Use mice with C57BL/6 background, aged 16-18 weeks, that express fluorescent calcium indicator constructs in the osteocytes. Osteocyte targeted expression is achieved by crossing flox-activated GCaMP6f and Dmp1-Cre mice. The details of breeding strategies and vendors for founder mice are described in a previously published study25.</li>
	<li>Sterilize all surgical tools, load bracket, water bath and fulcrum pin using an autoclave (57.2 &#176;C, 15 psi, 3-4 min). Disinfect microscope objectives with 100% ethanol.</li>
	<li>Turn on electronic components, including laser source, microscope, load cell, and actuator. Allow 15-20 min for each component to warm up prior to intravital imaging.
	<ol>
		<li>Make sure the actuator and load cell components are connected and activated in the control device. Generate the control software with a variety of platforms, including Matlab, LabView, and Python, according to the preferences of the user. The main Matlab code used in this study is called Actuator_Control_Software_withLoadCell.m (inside the MT3 Loading Device Control Software.zip folder Supplementary File 1). 
		&#8203;NOTE: Most commercially available two-photon microscope systems come with robust imaging software. The key features required for this method are the ability to tune a laser to the appropriate excitation for GCaMP6f (920 nm), the ability to adjust laser power intensity, and a time series collection with a frequency of at least 6 Hz. Prior to experimentation, laser connection to the imaging software and appropriate light path arrangement for two-photon imaging should be confirmed. This is confirmed in different ways depending on the imaging set up. Usually, there is a light indicator.</li>
	</ol>
	</li>
</ol>
2. Surgery
<ol>
	<li>Prepare a surgical stage and sterilize the surface with 70% ethanol. Ensure that aseptic techniques are employed throughout the surgical procedures. Maintain the&#160;level of cleanliness required for this protocol, as it is a terminal procedure.</li>
	<li>Anesthetize the mouse with vaporized isoflurane mixed with medical-grade air or oxygen at a flowrate of 1 L/min. Perform initial anesthetization in a rodent induction chamber with 3%-5% isoflurane. Maintain anesthesia at 1%-2.5% isoflurane in a nose cone for surgical and intravital imaging procedures.</li>
	<li>Place a heating device underneath or beside the mouse to assist in maintaining homeostatic core body temperature. Monitor the mouse&#39;s body temperature, heart rate, and oxygen saturation throughout the surgery. Keep the breath rate between 60-80 breaths per minute and maintain it by adjusting the isoflurane dosage.</li>
	<li>Place the mouse in a supine position. Confirm the depth of anesthesia before the incision via a toe pinch. Identify the location between the second and third metatarsals. Make a scalpel incision through the dermis between the second and third metatarsals, starting at the distal end and progressing proximally along the length of the bones (~5 mm). 
	NOTE: The metatarsals are distal to the ankle bones on the paw and follow directly proximal to the distal phalanges. They consist of (medial to lateral) metatarsals I, II, III, IV, and V. The third metatarsal is centered in the middle of the volar aspect of the hind paw.</li>
	<li>Using forceps, open the surgical site by pulling the skin toward the medial/lateral edges. Resect the extensor tendons using straight Vannas scissors to expose the third metatarsal.</li>
	<li>Insert the center fulcrum pin of the metatarsal loading device beneath the third metatarsal.
	<ol>
		<li>Initially, insert the pin in the small space at the distal end where the third metatarsal meets the proximal phalange and then move the pin proximally until it rests at the mid-shaft of the third metatarsal.</li>
		<li>Take special care to guarantee a direct interface between the bone and the pin, excluding any muscle and facia. This is critical for stable imaging during loading protocols.</li>
	</ol>
	</li>
	<li>Hold the ankle with forceps and place the foot into theDulbecco&#39;s phosphate-buffered saline (DPBS) filled water bath (8-10 mL). Secure the paw in place with the loading bracket and connect the bracket to the actuator/load cell arrangement. A completed surgical preparation and arrangement within the device is shown in Figure 1.</li>
</ol>
3. Imaging
NOTE: The complete two-photon microscopy setup used in this protocol has two software packages: Chameleon Discovery GUI V2.0.6 for the laser (Figure 2) and ThorImageLS4.0 for the microscope (Figure 3). To image on the two-photon, press Live (Figure 3, blue play button). When conducting an experiment to image and save data, press Capture (Figure 3, the tab at the top, next to Capture Setup). These are specific to the equipment and the vendors used in this experiment, but many alternatives with the necessary specifications found in this protocol (excitation wavelengths, viewable window size, image capture rate, etc.) would also work.
<ol>
	<li>Very carefully pick up the loading device setup with the mouse and place it onto the microscope platform.</li>
	<li>Start with a low magnification objective in epifluorescence mode (Figure 3, dropdown menu at the top with selections Multiphoton or Fluorescence Setup) to locate and center the mid-diaphysis of the bone.</li>
	<li>After a region of interest is located, switch to a higher water immersion objective magnification (20x-40x) and switch the optics to two-photon (Figure 3, dropdown menu at the top with selections Multiphoton or Fluorescence Setup). 
	NOTE: The recommended field of view size is at least 250 &#956;m x 250 &#956;m for cellular activity and can be achieved with either optical or digital zoom depending on the imaging system.
	<ol>
		<li>The suitable minimum pixel density is 512 pixels x 512 pixels. To set the pixel density, use the Galvo/Resonance Area Control settings (Figure 3).</li>
		<li>When finding the ROI, avoid photobleaching by reducing the power using the Power Control option (Figure 3,) and increasing the PMT amplification in the Galvo/Resonance Scanner Control settings (Figure 3).</li>
		<li>Identify the surface of the bone in two-photon mode by looking for the fibrous periosteum autofluorescence in the green channel that uses a bandpass filter centered at 525 nm. 
		NOTE: The autofluorescence is most visible with the excitation wavelength at 1,000 nm but is also available at 920 nm excitation (Figure 3, Multiphoton Laser Control). This landmark is important for determining the relative depth of the ROI into the metatarsal cortex when observing osteocytes. It should be noted that during time series experiments, the exact depth of the plane imaged is not recorded, although it tends to range between 15-30 &#181;m. If exact depth measurements are desired, then a z-stack would have to be taken.</li>
	</ol>
	</li>
	<li>Run a test loading bout to ensure the surgical preparation and positioning within the loading device were effective at achieving a stable ROI field (i.e., no z-plane displacement). Briefly, run a loading cycle to appraise the stability of the surgical preparation. Perform loading by running the section Switch on Servo and Move in the Matlab code.
	<ol>
		<li>Apply a small tare load. Ensure that the appropriate haversine wave loading protocols are prepared ahead of time. Input appropriate loading parameters obtained during calibration in section 1.2. Perform loading by running the section Switch on Servo and Move in the Matlab code.</li>
		<li>If there is a visible movement of the cells on-screen, which comes from micromotion of the bone in response to loading or breathing, select a different ROI along y- or z- directions to ensure it is directly over the center fulcrum pin. If movement persists, adjust the surgical position of the pin manually underneath the third metatarsal. 
		NOTE: A good region of interest (ROI) is one where the cells do not move in and out of the plane/focus. Movement in the x- and y-directions can be adjusted for post-processing using the template matching plugin on ImageJ.</li>
	</ol>
	</li>
	<li>Conduct z-stack or t-series imaging with loading according to the experimental design to record morphometric or dynamic load-induced signaling events, respectively.
	<ol>
		<li>Set the excitation wavelength for the fluorescent indicator (e.g., 920 nm for GCaMP6f). For z-stack, use a low enough resolution to capture features of the osteocytes, such as 0.25-1 &#956;m steps. For t-series, use settings to sample at least 6x the loading rate. For a 1 Hz loading rate, imaging at 6 frames per second (FPS) represents the minimally appropriate capture rate (Figure 3, Galvo/Resonance Scanner Control).</li>
		<li>For loading and live imaging, collect non-loaded baseline data with each bout. In this study, 60 s of non-loaded imaging followed by 60 s of loading and imaging is preferred. Design the loading and imaging protocols accordingly. To collect data, press Capture (Figure 3, tab at the top, next to Capture Setup).
		<ol>
			<li>The refractory period for a full calcium signaling response in bone cells is estimated to be approximately 15 min28. Wait at least that long between sequential loading bouts when collecting dynamic signaling data.</li>
			<li>Throughout the entire experiment, do not leave the animal unattended to ensure that it does not unexpectedly wake from anesthesia or experience distress without the opportunity for intervention. 
			NOTE: Euthanasia at the end of the procedure should be performed via cervical dislocation or other appropriate measures in accordance with IACUC-approved methods.&#160;This is a non-survival protocol meaning that all animals are euthanized after imaging.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>

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<li>Tian, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Imaging+neural+activity+in+worms%2C+flies+and+mice+with+improved+GCaMP+calcium+indicators%5BTitle%5D)+AND+%22Nature+Methods%22%5BJournal%5D)">Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators.</a> Nature Methods. 6 (12), 875-881 (2009).</li>
<li>Grienberger, C., Konnerth, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Imaging+calcium+in+neurons%5BTitle%5D)+AND+%22Neuron%22%5BJournal%5D)">Imaging calcium in neurons.</a> Neuron. 73 (5), 862-885 (2012).</li>
</ol>

The authors declare no conflicts of interest.

It is difficult to study osteocytes experimentally because of their embedded position in the hard tissue matrix, to which they rapidly deteriorate or dedifferentiate upon removal of this niche. Researching osteocytes has required immense ingenuity over the last 3 decades, such as the creation of osteocyte-like lines29,30,31, the establishment of protocols to isolate primary osteocytes32,<sup cl...

The bone matrix is organized according to mechanical demand1,2 and can change dynamically to account for shifting mechanical requirements3,4,5. Seminal work regarding the mechanosensory mechanism in bone was published as a modeling paper about 30 years ago6,7,8, where it was proposed that osteocytes embedded within the bone sense tissue level mechanical deformation via fluid movement in their local environment. This model was validated experimentally with in vitro and ex vivo experiments, where it was clearly shown that osteocytes are quite mechanosensitive1,2,3,4,5,6 and also express cytokines, which direct the behavior of bone building osteoblasts7 and osteoclasts8,9,10,11,12.
Calcium signaling is a ubiquitous second messenger that has been established as a central figure and dependable experimental target in osteocyte mechanobiology13,14,15,16. Calcium signaling has the advantage of being widely studied in cell biology17, which means there is a lot known about its downstream effects and the corresponding fluorescent tools available for experimental observation. In vitro analyses have used calcium signaling as a means of identifying osteocyte mechanical activation and characterizing dynamic signaling behavior5,18,19. Of note, observation of calcium signaling in an osteocyte cell line provided definitive evidence that fluid activation at the integrin attachments along the cell process is likely the main form of fluid flow activation20. This study is one of the many that showcase the utility of calcium signaling. It is reliably induced with the mechanical activation of osteocytes and thus serves as a potent target for interrogating osteocyte mechanobiology.
Osteocyte mechanotransduction in vivo is highly dependent on their immediate microenvironment. Matrix-binding proteins (e.g., proteoglycans, integrins) provide functional attachments between osteocyte cell membranes in an arrangement that is critical for fluid activation of the cell21,22. While two-dimensional (2D) in vitro analyses are helpful, they are limited in that they do not incorporate these critical three-dimensional (3D) features. Ex vivo preparations of osteocyte calcium signaling using confocal microscopy have shed some light on how osteocytes respond while keeping the surrounding matrix intact13,16. However, removing the blood supply from bone is thought to change the nutrients and fluid dynamics of the lacunocanalicular system. Interrogation of osteocyte mechanobiology requires in vivo investigation of load-induced osteocyte signaling.
In vivo investigation of embedded cells in bone has been largely hindered by the limitations of traditional imaging techniques, such as bright field and confocal microscopy. Osteocytes are positioned in a mineralized matrix23 composed of hydroxyapatite, collagen type 1, and other non-collagenous proteins that limit the optical accessibility24 and make the in vivo investigation technically challenging. However, recent advancements in non-linear fluorescent imaging and genetically encoded calcium reporters present the opportunity to overcome these challenges.
Here, we report a novel approach with the ability to image osteocytes in vivo to measure calcium signaling with cellular level resolution25. This is achieved by using a dynamic fluorescent marker using a genetically encoded calcium indicator for the first time in mouse osteocytes. Mice with DMP1-Cre driven osteocyte-targeted expression of GCaMP6f exhibit visible fluorescence in osteocytes throughout the diaphyseal cortex of mice metatarsals17,26. We use a three-point bending system in order to apply physiological levels of strain magnitude between 250-2,000 &#956;&#949;27. This technique allows for in vivo visualization of osteocyte calcium signaling dynamics during mechanical loading of the whole bone and could be useful to anyone seeking to understand osteocyte mechanobiology. This method would be appropriate for researchers seeking to expand their work from in vitro analyses to in vivo applications, especially while retaining functional-based molecular analyses (i.e., investigating cellular activity via calcium signaling) as opposed to broad-based phenotyping studies.

<table><tbody><tr><td>#3 Handle scalpel</td><td>Electron Microscopy Sciences</td><td>72040-03</td><td>Surgical supplies</td></tr><tr><td>20x Water immersion objective</td><td>Olympus</td><td>XLUMPLFLN20XW</td><td>This is a 20x objective, but 40x can also be used for this protocol. We recommend water immersions because it needs to be dipped in the bath during imaging, so open-air objective may cause abberrations</td></tr><tr><td>A.M. Bickford Omnicon F/AIR</td><td>AM Bickford</td><td>80120</td><td>A sensible answer to anesthesia gas problems in the operating room, the F/AIR anesthesia gas filter was specifically designed to remove waste anesthesia gases such as Isoflurane, Halothane, Enflurane, etc. from the operating room environment.</td></tr><tr><td>A.M. Bickford Omnicon F/AIR Kit&amp;nbsp;</td><td>AM Bickford</td><td>80000</td><td>An entire kit with tube and adaptors to connect F/AIR to setup</td></tr><tr><td>B6J.Cg-Gt(ROSA)26Sortm95.1(CAG-GCaMP6f)Hze/MwarJ</td><td>The Jackson Laboratory</td><td>28865</td><td>GCaMP6f Mice for cross-breeding with Dmp1-Cre mice</td></tr><tr><td>B6N.FVB-Tg(Dmp1-cre)1Jqfe/BwdJ</td><td>The Jackson Laboratory</td><td>23047</td><td>Dmp1-Cre Mice for cross-breeding with GCaMP6f&amp;nbsp; mice</td></tr><tr><td>Compression load cell</td><td>FUTEK Advanced Sensor Technology, Inc.</td><td>905898</td><td>LCM100 , 1000 g , Sub-miniature tension &amp;amp; compression load cell (Miniature/Inline Threaded) , RoHS lead free, Material - 17-4 PH S.S. , M3x0.5-thread , 34 Awg 4 conductor braided polyester cable , 5 ft Long</td></tr><tr><td>Corning 500 mL DPBS (Dulbecco&#039;s phosphate buffered saline), 1x [+] calcium, magnesium</td><td>VWR International</td><td>21-030-CV</td><td>Ionically balanced bath that contains calcium submerges the metatarsal during imaging</td></tr><tr><td>Dental pick tool</td><td>Electron Microscopy Sciences</td><td></td><td>Surgical supplies</td></tr><tr><td>Ethyl alcohol pure 200 proof ACS reagent &gt;99.5%</td><td>Sigma Aldrich</td><td>SIAL-459844-500ML</td><td>Sterilization purposes</td></tr><tr><td>Fulcrum pin</td><td>Fathom</td><td>N/A</td><td>Fabricated by direct 3D laser sintering of stainless steel (PH1 alloy) from 3D SolidWorks STL files. Original vendor was GPI Prototype &amp;amp; Manufacturing Services, Inc, now acquired by FATHOM, specifications are provided in the previously published document</td></tr><tr><td>High resolution and speed USB220 output kit</td><td>FUTEK Advanced Sensor Technology, Inc.</td><td>717435</td><td>Used to connect load cell to laptop</td></tr><tr><td>ImageJ 1.53t with Java 1.8.0_172 (for Windows 64-bit)</td><td>NIH</td><td>N/A</td><td>Install here https://imagej.nih.gov/ij/</td></tr><tr><td>Isoflurane</td><td>Piramal Critical Care</td><td>66794-013-25</td><td>100% inhalation vapour liquid</td></tr><tr><td>Loading bracket</td><td>Fathom</td><td>N/A</td><td>Fabricated by direct 3D laser sintering of stainless steel (PH1 alloy) from 3D SolidWorks STL files. Original vendor was GPI Prototype &amp;amp; Manufacturing Services, Inc, now acquired by FATHOM, specifications are provided in the previously published document</td></tr><tr><td>MATLAB R2019a</td><td>MathWorks</td><td></td><td>For running the loading device</td></tr><tr><td>Matrx VIP 3000 vaporizer well fill isoflurane</td><td>Butler Schein Animal Health</td><td>14309</td><td>Vaporizer for anesthetic</td></tr><tr><td>Nonin pulse oximeter Model 2500A Vet</td><td></td><td>2500A Vet</td><td></td></tr><tr><td>Piezo servo controller</td><td>PI-USA</td><td>E-625</td><td>Electronic component recommended by the company to be used with the actuator</td></tr><tr><td>PiezoMove high-stiffness linear piezo actuator</td><td>PI-USA</td><td>P-602.5SL</td><td>Actuator for the loading device</td></tr><tr><td>Scalpel blades, No. 10 for handle No. 3, pack of 100</td><td>Electron Microscopy Sciences</td><td>72044-10</td><td>Surgical supplies</td></tr><tr><td>Stainless steel tweezers with sharp, fine tips. Length: 120 mm</td><td>Electron Microscopy Sciences</td><td>78326-42</td><td>Surgical supplies</td></tr><tr><td>Thorlabs Bergamo multiphoton microscope</td><td>ThorLabs</td><td>N/A</td><td>This is only the imaging system and does not have the laser included, although ThorLabs has laser options if desired</td></tr><tr><td>Titanium-Saphire Chameleon Discovery NX with Total Power Control (TPC)</td><td>Coherent</td><td>N/A</td><td>This system technically has two lasers, both a tunable and a fixed laser. However, for the protocol, only the tunable is needed.&amp;nbsp;</td></tr><tr><td>Vannas spring scissors - 4 mm cutting edge</td><td>Fine Science Tools</td><td>15018-10</td><td>Surgical supplies</td></tr><tr><td>Water bath</td><td>Fathom</td><td>N/A</td><td>Fabricated by direct 3D laser sintering of stainless steel (PH1 alloy) from 3D SolidWorks STL files. Original vendor was GPI Prototype &amp;amp; Manufacturing Services, Inc, now acquired by FATHOM, specifications are provided in the previously published document</td></tr></tbody></table>

a fluorescent intravital imaging approach to study load-induced calcium signaling dynamics in mouse osteocytes

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

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.

Here we report a methodology for studying calcium signaling in embedded osteocytes in vivo using acute surgical preparation and multiphoton fluorescent imaging. Green fluorescent signal can be observed from genetically encoded calcium indicators in osteocytes via DMP1-Cre expression. Figure 4 is a single-plane image of embedded osteocytes. Note that all cells are labeled and express baseline green fluorescence, making it easy to find candidates for experimental observation....

The current article describes performing an intravital imaging approach to observe mechanically induced calcium signaling of embedded osteocytes in vivo in real-time in response to tissue-level mechanical loading of the mouse third metatarsal.

Bone tissue is exquisitely sensitive to differences in mechanical load magnitude. Osteocytes, dendritic cells that form a syncytium throughout the bone, ...

a-fluorescent-intravital-imaging-approach-to-study-load-induced

Research

JoVE Journal

Bioengineering

To understand network dynamics of microcircuits in the neocortex, it is essential to simultaneously record the activity of a large number of neurons .  In-vivo two-photon calcium imaging is the only method that allows one to record the activity of a dense neuronal population with single-cell resolution .

In Vivo 2-Photon Calcium Imaging in Layer 2/3 of Mice

The extent of store-operated Ca2+ entry (SOCE) can be monitored using fluorescent Ca2+ indicators. Mn2+ quenching of such indicators assays SOCE in cultured cells and skeletal muscle fibers. A technique allowing spatial and temporal resolution of SOCE by confocal imaging of mechanically skinned muscle fibers is also described.

Fluorescence-based Measurement of Store-operated Calcium Entry in Live Cells: from Cultured Cancer Cell to Skeletal Muscle Fiber

Source: Heredia, D. J., et. al. Ex Vivo Imaging of Cell-specific Calcium Signaling at the Tripartite Synapse of the Mouse Diaphragm. J. Vis. Exp. (2018) This video demonstrates fluorescence imaging of calcium dynamics at neuromuscular junctions (NMJs) in a transgenic mouse expressing genetically encoded calcium indicators. A NJM is identified by fluorescently tagged acetylcholine receptors in the diaphragm with the phrenic nerve. An image splitter is used to visualize multiple signals...

Fluorescence Imaging of Calcium Dynamics at Neuromuscular Junctions in the Diaphragm of a Transgenic Mouse

Here we present techniques for imaging local IP3-mediated Ca2+ events using fluorescence microscopy in intact mammalian cells loaded with Ca2+ indicators together with an algorithm that automates identification and analysis of these events.

Imaging Local Ca2+ Signals in Cultured Mammalian Cells

Here we present a protocol to image calcium signaling in populations of individual cell types at the murine neuromuscular junction.

Ex Vivo Imaging of Cell-specific Calcium Signaling at the Tripartite Synapse of the Mouse Diaphragm

We present the methodology for the isolation of murine myocytes and how to obtain voltage or calcium traces simultaneously with sarcomere shortening traces using fluorescence photometry with simultaneous digital cell geometry measurements.

Optical Imaging of Isolated Murine Ventricular Myocytes

We present a protocol to expose the brainstem of adult mouse from the ventral side. By using a gradient-refractive index lens with a miniature microscope, calcium imaging can be used to examine the activity of inferior olive neural somata in vivo.

In vivo Calcium Imaging in Mouse Inferior Olive

Two related methods are described to visualize subcellular events required for synaptic transmission. These protocols enable the real-time monitoring of the dynamics of presynaptic calcium influx and synaptic vesicle membrane fusion using live-cell imaging of in vitro cultured neurons.

Real-Time Fluorescent Measurement of Synaptic Functions in Models of Amyotrophic Lateral Sclerosis

The protocol describes the method of loading a fluorescent calcium dye through the cut nerve into mouse motor nerve terminals. In addition, a unique method for recording fast calcium transients in the peripheral nerve endings using confocal microscopy is presented.

Registration of Calcium Transients in Mouse Neuromuscular Junction with High Temporal Resolution using Confocal Microscopy

The present protocol describes making a large (6 x 3 mm2) cranial window using food wrap, transparent silicone, and cover glass. This cranial window allows in vivo wide-field and two-photon calcium imaging experiments in the same mouse.

In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window

This study outlines the method to visualize and develop three-dimensional (3D) models of osteocytes within the lacunar-canalicular network (LCN) for computational fluid dynamics (CFD) analysis. The generated models using this method help to understand osteocyte mechanosensation in healthy or diseased bones.

Analysis and Imaging of Osteocytes

Discover intravital imaging techniques to study calcium signaling dynamics in mouse osteocytes during mechanical loading. This method enables real-time observation of cellular responses in their native bone environment.

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

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