Advances in microscopy with new visualization possibilities often bring dramatic progress to our understanding of the intriguing cellular machinery. Picosecond optoacoustic micro‐spectroscopy is an optical technique based on ultrafast pump‐probe generation and detection of hypersound on time durations of picoseconds and length scales of nanometers. It is experiencing a renaissance as a versatile imaging tool for cell biology research after a plethora of applications in solid‐state physics. In this emerging context, this work reports on a dual‐probe architecture to carry out real‐time parallel detection of the hypersound propagation inside a cell that is cultured on a metallic substrate, and of the hypersound reflection at the metal/cell adhesion interface. Using this optoacoustic modality, several biophysical properties of the cell can be measured in a noncontact and label‐free manner. Its abilities are demonstrated with the multiple imaging of a mitotic macrophage‐like cell in a single run experiment. 相似文献
Label‐free optical projection tomography technique makes it possible for quantitative whole mouse embryo imaging without any exogenous contrast agent. Further details can be found in the article by Sungbea Ban, Nam Hyun Cho, Eunjung Min, et al. ( e201800481 ).
A novel capsule optoacoustic endoscopy (COE) system is built which provides high‐quality 360‐degree images of the entire lumen, specifically designed for typical dimensions of human esophagus. The pill‐shaped encapsulated probe consists of a novel and highly sensitive ultrasound transducer fitted with an integrated miniature pre‐amplifier. For the first time, ex vivo volumetric vascular network images to a depth of 2 mm in swine esophageal lining using COE are demonstrated. Further details can be found in the article by Hailong He, Antonios Stylogiannis, Parastoo Afshari, et al. ( e201800439 )
Optimized light delivery allows for single shot whole organ optoacoustic imaging. The authors present an optimized illumination concept for volumetric tomography that utilizes 3D printing in combination with custom‐made optical fiber illumination. The new approach showed a clear advantage over conventional, single‐sided illumination strategies by eliminating the need to correct for illumination variances and resulting in enhancement of the effective field of view, greater penetration depth and significant improvements in the overall image quality. Further details can be found in the article by Benedict Mc Larney, Johannes Rebling, Zhenyue Chen, et al. ( e201800387 )
This review is aimed at interpreting development and advantages of intravital imaging as an emerging invaluable methodology and summarizing related representative discoveries in bone physiologies and pathologies. It also indicates current limitations, further refinement, and extended application of intravital imaging in bone research. Further details can be found in the article by Yuhao Liu, Quan Yuan, and Shiwen Zhanget ( e201960075 ).
An ultrafast time‐stretch imaging technique for edge detection is demonstrated. The edge detection based on the optical directional derivative is realized by using differential detection. Since the edge detection is implemented in the physical layer, the computation complexity in the back‐end digital signal processing is very low. The blood red cells and cancer cells can be easily identified by distinguishing the edges. Further details can be found in the article by Bo Dai, LuHe, Lulu Zheng, Yongfeng Fu et al. ( e201800044 ).
A false‐colored and merged image of fresh, ex vivo rat kidney acquired using an excitation‐scanning hyperspectral imaging system. The spectral image was acquired using excitation wavelengths from 360 to 550 nm. Colors represent principal components extracted from a spectral image cube featuring no added labels or markers. Further details can be found in the article by Peter F. Favreau, Joshua A. Deal, Bradley Harris, et al. ( e201900183 ).
CARS microscopy was employed to monitor the reorganization of intracellular lipids and proteins, as well as cellular transformations, after irradiation with near infrared (NIR) light. NIR light was shown to induce apoptosis in HeLa cells in vitro in a dose‐dependent manner. The progression of apoptosis assessed with CARS microscopy is apparently associated with the generation of reactive oxygen species followed by an excessive formation of lipid droplets and their peroxidation. Further details can be found in the article by Svitlana M. Levchenko, Andrey N. Kuzmin, Artem Pliss, et al. ( e201900179 )
Nuclear pore complex imaged at three different resolutions by confocal, expansion, and Ex‐STED microscopy, respectively. NUP become a ruler to measure the expansion process. Further details can be found in the article by Luca Pesce, Marco Cozzolino, Luca Lanzanò, Alberto Diaspro, and Paolo Bianchini ( e201900018 ).
A new quantitative phase imaging (QPI) modality, coined multi‐ATOM, can now capture and process enormous amount of quantitative phase single‐cell images (>700,000 cells) at a ultrahigh throughput without compromising sub‐cellular resolution. It could empower label‐free single‐cell analysis where large‐scale and cost‐effective screening is necessary. Further details can be found in the article by Kelvin C. M. Lee, Andy K. S. Lau, Anson H. L. Tang, et al. ( e201800479 ).
Hyperspectral scanning laser optical tomography is developed to provide spectrally resolved volume data sets with high spectral resolution for large mesoscopic samples. It can be used to resolve largely overlapping fluorophores, as demonstrated by the 3D fluorescence hyperspectral reconstruction of a dual‐labelled mouse thymus gland sample and to distinguish between signals from autofluorescence of diseased and normal tissue without prior knowledge. Further details can be found in the article by Lingling Chen, Guiye Li, Li Tang, et al. ( e201800221 ).
A fast polarization‐resolved second harmonic generation microscope is implemented to map collagen orientation in thick and deforming tissues during mechanical assays. This system is based on line‐to‐line switching of the laser polarization using an electro‐optical modulator and works in epi‐detection geometry. After proper calibration, it successfully highlights the collagen dynamic alignment along the traction direction in ex vivo murine skin dermis. Further details can be found in the article by Guillaume Ducourthial, Jean‐Sébastien Affagard, Margaux Schmeltz, et al. ( e201800336 ).
A reflection‐mode switchable subwavelength Bessel‐beam (BB) and Gaussian‐beam (GB) photoacoustic microscopy (PAM) system has been developed. For the first time, the lateral resolution and the depth‐of‐field of the BB‐ and GB‐PAM were measured. It was demonstrated that BB‐PAM is a powerful tool for a wide range of biomedical research including RBC migration in blood vessels at various depths in vivo and observation of cell migration or cell culture. Further details can be found in the article by Byullee Park, Hoyong Lee, Seungwan Jeon, et al. ( e201800215 ).
Intraoperative margin assessment is clinically important, especially for tissue conserving surgery like Mohs micrographic surgery in which minimization of the surgical area is crucial. Instead of the complex frozen pathology protocol, slide‐free histopathological imaging of hematoxylin‐eosin stained whole‐mount skin tissues is demonstrated by using nonlinear microscopy, thus facilitating rapid intraoperative assessment of surgical tissues for future applications. Further details can be found in the article by Chi‐Kuang Sun, Chien‐Ting Kao, Ming‐Liang Wei, et al. ( e201800341 ).
Optoacoustics (OA) is combined with near‐infrared optical tomography (NIROT) in reflection mode to quantitatively image vasculature oxygen saturation (SO2) levels in phantoms containing vessels at depths up to 25 mm. Using NIROT to estimate the light fluence, the OA signals' spectral distortion was reduced from 60–150% to 10–20%. Results suggest that SO2 levels can be determined with <10% error and that temporal changes can be monitored with even better accuracy. Further details can be found in the article by Leonie Ulrich, Linda Ahnen, Hidayet Günhan Akarçay, et al. ( e201800112 ).
Two‐photon microscopy is the tool of choice for fluorescence imaging of deep tissues with high resolution, but can be limited in three‐dimensional acquisition speed and penetration depth. In this work, these issues are addressed by using an acoustic optofluidic lens capable of ultrafast beam shaping on a pixel basis. Driving the lens with different phase profiles enables high‐speed volumetric imaging, or enhanced signal‐to‐background for deeper penetration. Further details can be found in the article by Simonluca Piazza et al. ( e201700050 )
How does the ischemic tissue re‐vascularize? Now we can visualize the reperfusion process at high spatial resolution by using a dual‐wavelength MEMS scanning based optical resolution photoacoustic microscopy (OR‐PAM) system. The fast imaging capability enables continuous monitoring of skin reperfusion in a mouse model. It's also found that the ischemic tissue has a significantly higher oxygen consumption rate in the reperfusion stage comparing to the normal tissue. Further details can be found in the article by Renzhe Bi, U.S. Dinish, Chi Ching Goh, et al. ( e201800454 ).
iSERS (SERS=surface‐enhanced Raman scattering) microscopy is an emerging Raman‐based staining technique for the selective localization of target proteins on cells and tissues using antibody‐ SERS nanotag conjugates. In this contribution we demonstrate the feasibility of iSERS for imaging of programmed cell death‐ligand 1 (PD‐L1), an important predictive biomarker, on single SkBr‐3 breast cancer cells. Further details can be found in the article by Elzbieta Stepula, Matthias König, Xin‐Ping Wang, et al. ( e201960034 ).
Nonlinear photoperturbation of chromatin with femtosecond laser pulses. M. Tomas et al. present a novel method to visualize how the mobility of nuclear proteins changes in response to localized DNA damage. Picture: M. Tomas et al., 647–657 in this issue 相似文献
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