scholarly journals Visualizing the Role of Lipid Dynamics during Infrared Neural Stimulation with Hyperspectral Stimulated Raman Scattering Microscopy

2021 ◽  
Author(s):  
Wilson R Adams ◽  
Rekha Gautam ◽  
Andrea K Locke ◽  
Ana I Borrachero-Conejo ◽  
Bryan R Dollinger ◽  
...  

Infrared neural stimulation, or INS, is a method of using pulsed infrared light to yield label-free neuronal stimulation with broad experimental and translational utility. Despite its robust demonstration, the mechanistic and biophysical underpinnings of INS have been the subject of debate for more than a decade. The role of lipid membrane thermodynamics appears to play an important role in how fast IR-mediated heating nonspecifically drives action potential generation. Direct observation of lipid membrane dynamics during INS remains to be shown in a live neural model system. To directly test the involvement of lipid dynamics in INS, we used hyperspectral stimulated Raman scattering (hsSRS) microscopy to study biochemical signatures of high speed vibrational dynamics underlying INS in a live neural cell culture model. Findings suggest that lipid bilayer structural changes are occurring during INS in vitro in NG108-15 neuroglioma cells. Lipid-specific signatures of cell SRS spectra were found to vary with stimulation energy and radiant exposure. Spectroscopic observations were verified against high-speed ratiometric fluorescence imaging of a conventional lipophilic membrane structure reporter, di-4-ANNEPS. Overall, the presented data supports the hypothesis that INS causes changes in the lipid membrane of neural cells by changing lipid membrane packing order - which coincides with likelihood of cell stimulation. Furthermore, this work highlights the potential of hsSRS as a method to study biophysical and biochemical dynamics safely in live cells.

2019 ◽  
Vol 116 (32) ◽  
pp. 15842-15848 ◽  
Author(s):  
Yuta Suzuki ◽  
Koya Kobayashi ◽  
Yoshifumi Wakisaka ◽  
Dinghuan Deng ◽  
Shunji Tanaka ◽  
...  

Combining the strength of flow cytometry with fluorescence imaging and digital image analysis, imaging flow cytometry is a powerful tool in diverse fields including cancer biology, immunology, drug discovery, microbiology, and metabolic engineering. It enables measurements and statistical analyses of chemical, structural, and morphological phenotypes of numerous living cells to provide systematic insights into biological processes. However, its utility is constrained by its requirement of fluorescent labeling for phenotyping. Here we present label-free chemical imaging flow cytometry to overcome the issue. It builds on a pulse pair-resolved wavelength-switchable Stokes laser for the fastest-to-date multicolor stimulated Raman scattering (SRS) microscopy of fast-flowing cells on a 3D acoustic focusing microfluidic chip, enabling an unprecedented throughput of up to ∼140 cells/s. To show its broad utility, we use the SRS imaging flow cytometry with the aid of deep learning to study the metabolic heterogeneity of microalgal cells and perform marker-free cancer detection in blood.


1982 ◽  
Vol 12 (1) ◽  
pp. 35-37 ◽  
Author(s):  
R B Andreev ◽  
V A Gorbunov ◽  
S S Gulidov ◽  
S B Papernyĭ ◽  
V A Serebryakov

2018 ◽  
Vol 0 (0) ◽  
Author(s):  
Farman Ali ◽  
Yousaf Khan ◽  
Shahryar Shafique Qureshi ◽  
Shabir Ahmad ◽  
Muhammad Waqas

AbstractThe impact of major nonlinearities in optical fiber such as SRR (Stimulated Raman Scattering) and Four Wave Maxing (FWM) in cascaded amplifier Dense Wavelength Division Multiplexing optical long reach and high speed data rate transmission scheme have been investigated at different data rates. Pulse walk off effect is considered for the purpose of calculating Stimulated Raman Scattering (SRS) nonlinear factor. Examination has been accomplished to assess signal to noise ratio thinking about the consolidated impact of SRS and FWM within the sight of amplified spontaneous emission noise to achieve minutest noise at altered data rates.


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