New Angles on Neuronal Dendrites In Vivo

2007 ◽  
Vol 98 (6) ◽  
pp. 3770-3779 ◽  
Author(s):  
Werner Göbel ◽  
Fritjof Helmchen

Imaging technologies are well suited to study neuronal dendrites, which are key elements for synaptic integration in the CNS. Dendrites are, however, frequently oriented perpendicular to tissue surfaces, impeding in vivo imaging approaches. Here we introduce novel laser-scanning modes for two-photon microscopy that enable in vivo imaging of spatiotemporal activity patterns in dendrites. First, we developed a method to image planes arbitrarily oriented in 3D, which proved particularly beneficial for calcium imaging of parallel fibers and Purkinje cell dendrites in rat cerebellar cortex. Second, we applied free linescans—either through multiple dendrites or along a single vertically oriented dendrite—to reveal fast dendritic calcium dynamics in neocortical pyramidal neurons. Finally, we invented a ribbon-type 3D scanning method for imaging user-defined convoluted planes enabling simultaneous measurements of calcium signals along multiple apical dendrites. These novel scanning modes will facilitate optical probing of dendritic function in vivo.

2016 ◽  
Vol 54 (12) ◽  
pp. 1343-1404
Author(s):  
A Ghallab ◽  
R Reif ◽  
R Hassan ◽  
AS Seddek ◽  
JG Hengstler

2017 ◽  
Vol 10 (11) ◽  
pp. 1526-1537 ◽  
Author(s):  
Y. X. Li ◽  
V. Gautam ◽  
A. Brüstle ◽  
I. A. Cockburn ◽  
V. R. Daria ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Seokchan Yoon ◽  
Hojun Lee ◽  
Jin Hee Hong ◽  
Yong-Sik Lim ◽  
Wonshik Choi

AbstractA mouse skull is a barrier for high-resolution optical imaging because its thick and inhomogeneous internal structures induce complex aberrations varying drastically from position to position. Invasive procedures creating either thinned-skull or open-skull windows are often required for the microscopic imaging of brain tissues underneath. Here, we propose a label-free imaging modality termed laser scanning reflection-matrix microscopy for recording the amplitude and phase maps of reflected waves at non-confocal points as well as confocal points. The proposed method enables us to find and computationally correct up to 10,000 angular modes of aberrations varying at every 10 × 10 µm2 patch in the sample plane. We realized reflectance imaging of myelinated axons in vivo underneath an intact mouse skull, with an ideal diffraction-limited spatial resolution of 450 nm. Furthermore, we demonstrated through-skull two-photon fluorescence imaging of neuronal dendrites and their spines by physically correcting the aberrations identified from the reflection matrix.


2015 ◽  
Vol 6 (9) ◽  
pp. 3303 ◽  
Author(s):  
Seoyeon Bok ◽  
Taejun Wang ◽  
Chan-Ju Lee ◽  
Seong-Uk Jeon ◽  
Young-Eun Kim ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (96) ◽  
pp. 94200-94205 ◽  
Author(s):  
Zheng Zheng ◽  
Flavien Caraguel ◽  
Yuan-Yuan Liao ◽  
Chantal Andraud ◽  
Boudewijn van der Sanden ◽  
...  

A new non-diffusible fluorescent probe for two photon microscopy, comprising a hydrophobic push-pull dye in the apolar core of Pluronic F127–silica nanoparticles, shows intense red emission (Φf 39% at 650 nm) and two-photon absorption properties in the NIR.


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