Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue: Detection Calcium Waves using Multiscale Vision Model

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue : Detection Calcium Waves using Multiscale Vision Model. / Brazhe, Alexey; Mathiesen, Claus; Lauritzen, Martin.

In: NeuroImage, Vol. 68, 03.2013, p. 192-202.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Brazhe, A, Mathiesen, C & Lauritzen, M 2013, 'Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue: Detection Calcium Waves using Multiscale Vision Model', NeuroImage, vol. 68, pp. 192-202. https://doi.org/10.1016/j.neuroimage.2012.11.024

APA

Brazhe, A., Mathiesen, C., & Lauritzen, M. (2013). Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue: Detection Calcium Waves using Multiscale Vision Model. NeuroImage, 68, 192-202. https://doi.org/10.1016/j.neuroimage.2012.11.024

Vancouver

Brazhe A, Mathiesen C, Lauritzen M. Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue: Detection Calcium Waves using Multiscale Vision Model. NeuroImage. 2013 Mar;68:192-202. https://doi.org/10.1016/j.neuroimage.2012.11.024

Author

Brazhe, Alexey ; Mathiesen, Claus ; Lauritzen, Martin. / Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue : Detection Calcium Waves using Multiscale Vision Model. In: NeuroImage. 2013 ; Vol. 68. pp. 192-202.

Bibtex

@article{fdb3a30740884a56b67d53202516c8e6,
title = "Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue: Detection Calcium Waves using Multiscale Vision Model",
abstract = "Intercellular glial calcium waves constitute a signaling pathway which can be visualized by fluorescence imaging of cytosolic Ca2+ changes. However, there is a lack of procedures for sensitive and reliable detection of calcium waves in noisy multiphoton imaging data. Here we extend multiscale vision model based on the undecimated wavelet transform for detection and extraction of calcium wave events in cerebellar cortex in vivo. In experimental data and validation studies using simulated data, the detection and characterization of glial calcium waves was significantly improved as compared to conventional analysis based on pixel thresholding. The described method allowed to visualize the underlying complexity of the glial networks as a prolonged Ca2+ elevation was observed at the origin of the wave, which could connect several recurrent waves separated by short time gaps, the data suggested a possible interplay between the waves and interneurons and the expanding front of the waves cold take variable forms and sometimes deviated from simple geometrical shapes, being jagged or making curved spurts when occurring near a blood vessel or a location of a previous wave. The calcium waves sprawled along blood vessels where propagation apparently occurred from end-foot to end-foot and was faster than away from vessels. Thus, small and large networks of molecular layer astrocytes and Bergmann glia can be activated in intercellular calcium waves, which are of potential importance for synaptic function and blood flow control. ",
author = "Alexey Brazhe and Claus Mathiesen and Martin Lauritzen",
year = "2013",
month = mar,
doi = "10.1016/j.neuroimage.2012.11.024",
language = "English",
volume = "68",
pages = "192--202",
journal = "NeuroImage",
issn = "1053-8119",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Multiscale Vision Model Highlights Spontaneous Glial Calcium Waves Recorded by 2-Photon Imaging in Brain Tissue

T2 - Detection Calcium Waves using Multiscale Vision Model

AU - Brazhe, Alexey

AU - Mathiesen, Claus

AU - Lauritzen, Martin

PY - 2013/3

Y1 - 2013/3

N2 - Intercellular glial calcium waves constitute a signaling pathway which can be visualized by fluorescence imaging of cytosolic Ca2+ changes. However, there is a lack of procedures for sensitive and reliable detection of calcium waves in noisy multiphoton imaging data. Here we extend multiscale vision model based on the undecimated wavelet transform for detection and extraction of calcium wave events in cerebellar cortex in vivo. In experimental data and validation studies using simulated data, the detection and characterization of glial calcium waves was significantly improved as compared to conventional analysis based on pixel thresholding. The described method allowed to visualize the underlying complexity of the glial networks as a prolonged Ca2+ elevation was observed at the origin of the wave, which could connect several recurrent waves separated by short time gaps, the data suggested a possible interplay between the waves and interneurons and the expanding front of the waves cold take variable forms and sometimes deviated from simple geometrical shapes, being jagged or making curved spurts when occurring near a blood vessel or a location of a previous wave. The calcium waves sprawled along blood vessels where propagation apparently occurred from end-foot to end-foot and was faster than away from vessels. Thus, small and large networks of molecular layer astrocytes and Bergmann glia can be activated in intercellular calcium waves, which are of potential importance for synaptic function and blood flow control.

AB - Intercellular glial calcium waves constitute a signaling pathway which can be visualized by fluorescence imaging of cytosolic Ca2+ changes. However, there is a lack of procedures for sensitive and reliable detection of calcium waves in noisy multiphoton imaging data. Here we extend multiscale vision model based on the undecimated wavelet transform for detection and extraction of calcium wave events in cerebellar cortex in vivo. In experimental data and validation studies using simulated data, the detection and characterization of glial calcium waves was significantly improved as compared to conventional analysis based on pixel thresholding. The described method allowed to visualize the underlying complexity of the glial networks as a prolonged Ca2+ elevation was observed at the origin of the wave, which could connect several recurrent waves separated by short time gaps, the data suggested a possible interplay between the waves and interneurons and the expanding front of the waves cold take variable forms and sometimes deviated from simple geometrical shapes, being jagged or making curved spurts when occurring near a blood vessel or a location of a previous wave. The calcium waves sprawled along blood vessels where propagation apparently occurred from end-foot to end-foot and was faster than away from vessels. Thus, small and large networks of molecular layer astrocytes and Bergmann glia can be activated in intercellular calcium waves, which are of potential importance for synaptic function and blood flow control.

U2 - 10.1016/j.neuroimage.2012.11.024

DO - 10.1016/j.neuroimage.2012.11.024

M3 - Journal article

C2 - 23219568

VL - 68

SP - 192

EP - 202

JO - NeuroImage

JF - NeuroImage

SN - 1053-8119

ER -

ID: 38471907