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Mechanical mapping of spinal cord development and repair in living zebrafish larvae using Brillouin microscopy

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Axonal regrowth after spinal cord transection in adult zebrafish
inferredcites →https://doi.org/10.1002/cne.1131openalex-snapshot
Regenerating descending axons preferentially reroute to the gray matter in the presence of a general macrophage/microglial reaction caudal to a spinal transection in adult zebrafish
inferredcites →https://doi.org/10.1002/cne.23115openalex-snapshot
Lesion‐induced generation of interneuron cell types in specific dorsoventral domains in the spinal cord of adult zebrafish
inferredcites →https://doi.org/10.1002/dvdy.22438openalex-snapshot
Cellular response after crush injury in adult zebrafish spinal cord
inferredcites →https://doi.org/10.1002/jbio.201500273openalex-snapshot
Cell nuclei have lower refractive index and mass density than cytoplasm
inferredcites →https://doi.org/10.1002/jbio.201700145openalex-snapshot
Three‐dimensional correlative single‐cell imaging utilizing fluorescence and refractive index tomography
inferredcites →https://doi.org/10.1002/jez.b.21381openalex-snapshot
Structural components and morphogenetic mechanics of the zebrafish yolk extension, a developmental module
inferredcites →https://doi.org/10.1002/nbm.3319openalex-snapshot
Tissue structure and inflammatory processes shape viscoelastic properties of the mouse brain
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Transverse Elasticity of Myofibrils of Rabbit Skeletal Muscle Studied by Atomic Force Microscopy
inferredcites →https://doi.org/10.1007/s1012601-0053-4openalex-snapshot
Generating Transparent Zebrafish: A Refined Method to Improve Detection of Gene Expression During Embryonic Development
inferredcites →https://doi.org/10.1007/s11249-006-9073-0openalex-snapshot
Experimental investigation of frictional and viscoelastic properties of intestine for microendoscope application
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Atomic force microscopy-based force measurements on animal cells and tissues
inferredcites →https://doi.org/10.1016/j.biocel.2012.02.003openalex-snapshot
Transcription factor regulation by mechanical stress
inferredcites →https://doi.org/10.1016/j.biomaterials.2014.01.038openalex-snapshot
The relationship between glial cell mechanosensitivity and foreign body reactions in the central nervous system
inferredcites →https://doi.org/10.1016/j.bpj.2008.10.064openalex-snapshot
Axisymmetric Drop Shape Analysis for Estimating the Surface Tension of Cell Aggregates by Centrifugation
inferredcites →https://doi.org/10.1016/j.bpj.2011.08.008openalex-snapshot
In Vivo Measurement of Age-Related Stiffening in the Crystalline Lens by Brillouin Optical Microscopy
inferredcites →https://doi.org/10.1016/j.bpj.2015.03.039openalex-snapshot
CNS Cell Distribution and Axon Orientation Determine Local Spinal Cord Mechanical Properties
inferredcites →https://doi.org/10.1016/j.bpj.2017.06.069openalex-snapshot
Passive and Active Microrheology of the Intestinal Fluid of the Larval Zebrafish
inferredcites →https://doi.org/10.1016/j.ceb.2013.04.010openalex-snapshot
Mechanical guidance of cell migration: lessons from chemotaxis
inferredcites →https://doi.org/10.1016/j.cell.2006.06.044openalex-snapshot
Matrix Elasticity Directs Stem Cell Lineage Specification
inferredcites →https://doi.org/10.1016/j.cub.2009.07.069openalex-snapshot
Cell-Cycle Control by Physiological Matrix Elasticity and In Vivo Tissue Stiffening
inferredcites →https://doi.org/10.1016/j.expneurol.2014.03.017openalex-snapshot
Radial glial progenitors repair the zebrafish spinal cord following transection
inferredcites →https://doi.org/10.1016/j.jbiomech.2008.02.007openalex-snapshot
Viscoelastic properties of passive skeletal muscle in compression: Stress-relaxation behaviour and constitutive modelling
inferredcites →https://doi.org/10.1016/j.jbiomech.2010.07.002openalex-snapshot
Mechanical difference between white and gray matter in the rat cerebellum measured by scanning force microscopy
inferredcites →https://doi.org/10.1016/j.jneumeth.2016.07.002openalex-snapshot
Brain tissue stiffness is a sensitive marker for acidosis
inferredcites →https://doi.org/10.1016/j.ydbio.2014.12.005openalex-snapshot
Tissue mechanics and adhesion during embryo development
inferredcites →https://doi.org/10.1016/j.ydbio.2015.03.025openalex-snapshot
Wnt/ß-catenin signaling is required for radial glial neurogenesis following spinal cord injury
inferredcites →https://doi.org/10.1016/s0006-3495(00)76279-5openalex-snapshot
Cell Movement Is Guided by the Rigidity of the Substrate
inferredcites →https://doi.org/10.1016/s0006-3495(01)75740-2openalex-snapshot
The Optical Stretcher: A Novel Laser Tool to Micromanipulate Cells
inferredcites →https://doi.org/10.1016/s0165-0270(99)00008-4openalex-snapshot
In vivo recording from identifiable neurons of the locomotor network in the developing zebrafish
inferredcites →https://doi.org/10.1016/s0361-9230(99)00072-6openalex-snapshot
The glial scar and central nervous system repair
inferredcites →https://doi.org/10.1038/169366b0openalex-snapshot
Interference Microscopy and Mass Determination
inferredcites →https://doi.org/10.1038/169541a0openalex-snapshot
Interference Microscopy and Mass Determination
inferredcites →https://doi.org/10.1038/ncomms10974openalex-snapshot
Optical micromanipulation of nanoparticles and cells inside living zebrafish
inferredcites →https://doi.org/10.1038/ncomms14787openalex-snapshot
The soft mechanical signature of glial scars in the central nervous system
inferredcites →https://doi.org/10.1038/nmeth.3175openalex-snapshot
Live-cell mass profiling: an emerging approach in quantitative biophysics
inferredcites →https://doi.org/10.1038/nmeth.3616openalex-snapshot
Noncontact three-dimensional mapping of intracellular hydromechanical properties by Brillouin microscopy
inferredcites →https://doi.org/10.1038/nmeth.4101openalex-snapshot
In vivo quantification of spatially varying mechanical properties in developing tissues
inferredcites →https://doi.org/10.1038/nn.4394openalex-snapshot
Mechanosensing is critical for axon growth in the developing brain
inferredcites →https://doi.org/10.1038/nphoton.2007.250openalex-snapshot
Confocal Brillouin microscopy for three-dimensional mechanical imaging
inferredcites →https://doi.org/10.1038/nrn1326openalex-snapshot
Regeneration beyond the glial scar
inferredcites →https://doi.org/10.1038/s41467-017-00143-0openalex-snapshot
Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish
inferredcites →https://doi.org/10.1038/srep33084openalex-snapshot
Holographic intravital microscopy for 2-D and 3-D imaging intact circulating blood cells in microcapillaries of live mice
inferredcites →https://doi.org/10.1039/c0sm01017kopenalex-snapshot
Spatial mapping of the mechanical properties of the living retina using scanning force microscopy
inferredcites →https://doi.org/10.1039/c3sm50552aopenalex-snapshot
Structure-sensitive elastography: on the viscoelastic powerlaw behavior of in vivo human tissue in health and disease
inferredcites →https://doi.org/10.1051/anphys/192209170088openalex-snapshot
Diffusion de la lumière et des rayons X par un corps transparent homogène
inferredcites →https://doi.org/10.1063/1.3095471openalex-snapshot
Bulk viscosity and compressibility measurement using acoustic spectroscopy
inferredcites →https://doi.org/10.1063/1.447892openalex-snapshot
Rayleigh–Brillouin spectroscopy of simple viscoelastic liquids
inferredcites →https://doi.org/10.1063/1.4836477openalex-snapshot
Spectral broadening in Brillouin imaging
inferredcites →https://doi.org/10.1073/pnas.0606150103openalex-snapshot
Viscoelastic properties of individual glial cells and neurons in the CNS
inferredcites →https://doi.org/10.1073/pnas.1003743107openalex-snapshot
Coaction of intercellular adhesion and cortical tension specifies tissue surface tension
inferredcites →https://doi.org/10.1073/pnas.112194999openalex-snapshot
Binding strength and activation state of single fibrinogen-integrin pairs on living cells
inferredcites →https://doi.org/10.1073/pnas.1418732112openalex-snapshot
Direct laser manipulation reveals the mechanics of cell contacts in vivo
inferredcites →https://doi.org/10.1083/jcb.200405004openalex-snapshot
Myotubes differentiate optimally on substrates with tissue-like stiffness
inferredcites →https://doi.org/10.1083/jcb.201212095openalex-snapshot
Notochord vacuoles are lysosome-related organelles that function in axis and spine morphogenesis
inferredcites →https://doi.org/10.1088/0034-4885/45/3/002openalex-snapshot
Brillouin scattering in condensed matter
inferredcites →https://doi.org/10.1088/0034-4885/73/9/094601openalex-snapshot
The biophysics of neuronal growth
inferredcites →https://doi.org/10.1088/0953-8984/22/19/194114openalex-snapshot
Mechanosensitivity of astrocytes on optimized polyacrylamide gels analyzed by quantitative morphometry
inferredcites →https://doi.org/10.1088/1478-3975/aa6d18openalex-snapshot
The role of cell body density in ruminant retina mechanics assessed by atomic force and Brillouin microscopy
inferredcites →https://doi.org/10.1089/scd.2012.0189openalex-snapshot
Mechanical Environment Modulates Biological Properties of Oligodendrocyte Progenitor Cells
inferredcites →https://doi.org/10.1093/icb/40.1.28openalex-snapshot
Mechanical Design of Fiber-Wound Hydraulic Skeletons: The Stiffening and Straightening of Embryonic Notochords
inferredcites →https://doi.org/10.1093/ilar.53.2.192openalex-snapshot
Anesthesia and Euthanasia in Zebrafish
inferredcites →https://doi.org/10.1093/oso/9780199638086.003.0002openalex-snapshot
Keeping and raising zebrafish
inferredcites →https://doi.org/10.1097/00001756-200212200-00007openalex-snapshot
Neurite branching on deformable substrates
inferredcites →https://doi.org/10.1098/rsif.2015.0843openalex-snapshot
Quantification of plaque stiffness by Brillouin microscopy in experimental thin cap fibroatheroma
inferredcites →https://doi.org/10.1101/cshperspect.a020602openalex-snapshot
Central Nervous System Regenerative Failure: Role of Oligodendrocytes, Astrocytes, and Microglia
inferredcites →https://doi.org/10.1109/iccv.2011.6126544openalex-snapshot
ORB: An efficient alternative to SIFT or SURF
inferredcites →https://doi.org/10.1109/jqe.2004.825210openalex-snapshot
A Dispersion Law for Virtually Imaged Phased-Array Spectral Dispersers Based on Paraxial Wave Theory
inferredcites →https://doi.org/10.1115/1.4003131openalex-snapshot
Micro-Brillouin Scattering Measurements in Mature and Newly Formed Bone Tissue Surrounding an Implant
inferredcites →https://doi.org/10.1117/12.2213978openalex-snapshot
Watching embryonic development in a new light: elasticity specific imaging with dual Brillouin/Raman microspectroscopy
inferredcites →https://doi.org/10.1119/1.1286663openalex-snapshot
An introduction to Pound–Drever–Hall laser frequency stabilization
inferredcites →https://doi.org/10.1126/science.1116995openalex-snapshot
Tissue Cells Feel and Respond to the Stiffness of Their Substrate
inferredcites →https://doi.org/10.1126/science.1225399openalex-snapshot
Adhesion Functions in Cell Sorting by Mechanically Coupling the Cortices of Adhering Cells
inferredcites →https://doi.org/10.1126/science.aaf2679openalex-snapshot
Injury-induced ctgfa directs glial bridging and spinal cord regeneration in zebrafish
inferredcites →https://doi.org/10.1126/scisignal.aaf6326openalex-snapshot
Mapping the subcellular mechanical properties of live cells in tissues with fluorescence emission–Brillouin imaging
inferredcites →https://doi.org/10.1146/annurev-bioeng-071811-150045openalex-snapshot
Mechanics in Neuronal Development and Repair
inferredcites →https://doi.org/10.1146/annurev.bioeng.5.040202.121623openalex-snapshot
Selected Methods for Imaging Elastic Properties of Biological Tissues
inferredcites →https://doi.org/10.1152/ajpcell.00121.2008openalex-snapshot
Optical imaging of cell mass and growth dynamics
inferredcites →https://doi.org/10.1152/jn.01248.2004openalex-snapshot
Fictive Swimming Motor Patterns in Wild Type and Mutant Larval Zebrafish
inferredcites →https://doi.org/10.1158/0008-5472.can-08-4859openalex-snapshot
The Mechanical Rigidity of the Extracellular Matrix Regulates the Structure, Motility, and Proliferation of Glioma Cells
inferredcites →https://doi.org/10.1158/0008-5472.sabcs-4167openalex-snapshot
RANKL inhibition decreases the incidence of mammary adenocarcinomas in wild type (WT) and MMTV-RANK transgenic mice.
inferredcites →https://doi.org/10.1167/iovs.14-14450openalex-snapshot
Biomechanical Characterization of Keratoconus Corneas Ex Vivo With Brillouin Microscopy
inferredcites →https://doi.org/10.1242/dev.01812openalex-snapshot
Structure and function of the notochord: an essential organ for chordate development
inferredcites →https://doi.org/10.1242/dev.109637openalex-snapshot
Systematic profiling of spatiotemporal tissue and cellular stiffness in the developing brain
inferredcites →https://doi.org/10.1242/dev.129155openalex-snapshot
Spinal motor neurons are regenerated after mechanical lesion and genetic ablation in larval zebrafish
inferredcites →https://doi.org/10.1364/aop.8.000300openalex-snapshot
Seeing cells in a new light: a renaissance of Brillouin spectroscopy
inferredcites →https://doi.org/10.1364/oe.19.010913openalex-snapshot
Multistage VIPA etalons for high-extinction parallel Brillouin spectroscopy
inferredcites →https://doi.org/10.1364/oe.20.009197openalex-snapshot
In vivo Brillouin optical microscopy of the human eye
inferredcites →https://doi.org/10.1364/oe.22.005410openalex-snapshot
Background clean-up in Brillouin microspectroscopy of scattering medium
inferredcites →https://doi.org/10.1364/ol.33.002979openalex-snapshot
Cross-axis cascading of spectral dispersion
inferredcites →https://doi.org/10.1371/journal.pone.0143595openalex-snapshot
Characterization of Proliferating Neural Progenitors after Spinal Cord Injury in Adult Zebrafish
inferredcites →https://doi.org/10.1523/jneurosci.0758-12.2012openalex-snapshot
Fgf-Dependent Glial Cell Bridges Facilitate Spinal Cord Regeneration in Zebrafish
inferredcites →https://doi.org/10.1523/jneurosci.1189-08.2008openalex-snapshot
Motor Neuron Regeneration in Adult Zebrafish
inferredcites →https://doi.org/10.1668/0003-1569(2000)040[0028:mdofwh]2.0.co;2openalex-snapshot
Mechanical Design of Fiber-Wound Hydraulic Skeletons: The Stiffening and Straightening of Embryonic Notochords1
inferredcites →https://doi.org/10.2174/157340511798038684openalex-snapshot
An Overview of Elastography-An Emerging Branch of Medical Imaging
inferredcites →https://doi.org/10.3181/0710-mr-278openalex-snapshot
Measurement Techniques for Cellular Biomechanics In Vitro
inferredcites →https://doi.org/10.3233/rnn-2008-00443openalex-snapshot
Adult zebrafish as a model for successful central nervous system regeneration
inferredcites →https://doi.org/10.3791/53468openalex-snapshot
High Speed Sub-GHz Spectrometer for Brillouin Scattering Analysis
inferredcites →https://doi.org/10.3791/53468-vopenalex-snapshot
High Speed Sub-GHz Spectrometer for Brillouin Scattering Analysis
inferredcites →https://doi.org/10.3938/jkps.51.854openalex-snapshot
Measurement of Micro-Elasticity within a Fertilized Egg by Using Brillouin Scattering Spectroscopy

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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