Search bioRxiv⌕ Search

Biology subjects

Koukourakis, N.

Publications and source records attributed to Koukourakis, N..

3 recordsLinked to original sources

Understanding Virtual Staining with generative adversarial networks for Osteoclast Imaging

Virtual staining with generative adversarial networks is an efficient, non-invasive and scalable alternative to conventional cell staining, minimizing the need for destructive and time-consuming protocols. In this study, we investigate the explainability of a network trained to virtually stain osteoclast cultures, using intensity-based label-free input images. The model enables analysis of cell cultures without immunostaining. Explainability assessments, including receptive field and feature map analyses, show that the background in input images significantly influences staining predictions within cellular regions and the trained network performs an internal segmentation during the image transformation process. This suggests that contextual cues beyond cell boundaries are implicitly learned and integrated during training. By eliminating repetitive staining procedures, virtual staining enables longitudinal studies, allows multiplexing of individual samples, and reduces reagents and laboratory waste. Our findings enhance understanding of the virtual staining process and highlight its potential for biomedical research applications.

bioengineering↗

Single-shot impulsive stimulated Brillouin microscopy by tailored ultrashort pulses

Brillouin microscopy has become an important tool for investigating the mechanical properties of tissue. The recently developed Impulsive stimulated Brillouin Scattering (ISBS) promises a label-free, non-invasive measurements of viscoelastic properties of transparent samples and offers the potential for a high temporal resolution. However, the spatial resolution of ISBS is currently limited, which hinders its transfer to real-world applications. Increasing the spatial resolution of ISBS leads to an increase in the energy density of the pump beams, which requires a balancing of the excitation parameters to stay below the phototoxic threshold. This paper focuses on the influences of different excitation parameters on the spatial, temporal and spectral resolution and their optimal values. Combined with the adoption of a noise suppressing window function, a measurement rate of 20{micro}s/pixel in hydrogel is achieved, which is promising for fast 3D imaging. The presented advanced impulsive stimulated Brillouin microscopy can be applied for fast tissue elastography to-ward disease studies.

biophysics↗

In situ measurement of the isoplanatic patch for imaging through intact bone

Wavefront-shaping (WS) enables imaging through scattering tissues like bone, which is important for neuroscience and bone-regeneration research. WS corrects for the optical aberrations at a given depth and field-of-view (FOV) within the sample; the extent of the validity of which is limited to a region known as the isoplanatic patch (IP). Knowing this parameter helps to estimate the number of corrections needed for WS imaging over a given FOV. In this paper, we first present direct transmissive measurement of murine skull IP using digital optical phase conjugation (DOPC) based focusing. Second, we extend our previously reported Phase Accumulation Ray Tracing (PART) method to provide in-situ in-silico estimation of IP, called correlative PART (cPART). Our results show an IP range of 1-3 m for mice within an age range of 8-14 days old and 1.00{+/-}0.25 m in a 12-week old adult skull. Consistency between the two measurement approaches indicates that cPART can be used to approximate the IP before a WS experiment, which can be used to calculate the number of corrections required within a given field of view. Abstract Figure O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=195 SRC="FIGDIR/small/246595v1_ufig1.gif" ALT="Figure 1"> View larger version (56K): org.highwire.dtl.DTLVardef@1844a5eorg.highwire.dtl.DTLVardef@2e80dforg.highwire.dtl.DTLVardef@10ecd49org.highwire.dtl.DTLVardef@c7afa9_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗