In recent years, the dynamic role of Lipid Droplets (LDs) in many cellular activities has been increasingly brought to light. In fact, it has been discovered that LDs are involved in many pathologies (e.g., diabetes, atherosclerosis, pathogen infections, neurodegenerative diseases and cancer). Moreover, it has been demonstrated that their number and size increase during an inflammation or infectious inside the immune cells, also with the COVID-19. Therefore, detecting LDs within single cells could aid the diagnosis of several pathologies. Currently, the gold-standard technique in this field is Fluorescence Imaging Flow Cytometry (FIFC), in which the single-cell analysis of fluorescence microscopy is implemented in high-throughput modality thanks to the flow-cytometry module. However, to overcome the drawbacks related to the fluorescence staining, Holographic Imaging Flow Cytometry (HIFC) has gaining momentum as label-free alternative to the FIFC tool. Thanks to the interferometric principles at the basis of digital holography, it has been already demonstrated that a suspended cell acts as a biological lens with specific focusing features. Here we show that the presence of intracellular LDs inside the cell is able to change its focalization features, measured through a HIFC system. Therefore, based on this property, we demonstrate that a detection of single cells containing intracellular LDs is possible by means of a direct analysis of the digital holograms recorded in flow cytometry modality. The attained results open the route to the development of a fast, non-destructive, and high-throughput tool for the diagnosis of LDs-related pathologies by exploiting the biolens’ signature in HIFC.
Detection and quantification of intracellular structures is fundamental in biomedical sciences. New emerging inspection tools based on holographic microscopy and quantitative phase imaging can give answers to such critical demands. Holographic tomography (HT) systems are the best candidates for this challenge. Recently, HT has been demonstrated working in flow-cytometry (FC) modality. Results show that the novel HTFC tool is capable to furnish 3D visualization and quantifications of the different intracellular particles. In particular, here we report that exogenous nanographene oxide particles as well as endogenous lipid droplets can be detected, measured, and visualized in each flowing cell by label-free HTFC. This method opens the way for accurate and high-throughput measurements at the 3D single-cell level for different applications such as diagnosis of diseases, development of drug delivery applications, and examination of cell functionalities. Experiments and processing methods will be described, and several examples will be discussed.
Tomographic phase microscopy in cytometry environment is feasible at single cell level and without the a-priori knowledge of the cell orientation. In the present paper we demonstrate different strategies for recovery the rotation angles of single cells and clusters when rotating into microfluidic channels, thus realistically opening to the implementation of marker-free cytofluorimeter for three-dimensional imaging of biological fluids. The pioneering developed strategies allows to measure quantitatively the inner distribution of the refractive indexes inside the cell volume avoiding the use of chemical and fluorescent tags. The imaging apparatus is based on label-free Digital Holography in microscopy setup designed in transmission geometry to image 700x700μm Field of View with lateral resolution of 0.5μm. Digital Holography is perfectly suited for imaging in microchannels as it allows the numerical refocusing of sample into a three-dimensional volume. In the present paper, such imaging arrangement is combined with a high-precision pumping system connected to a microfluidic channel that allow the complete rotation of the flowing cells into the Field of View. High-speed 25Megapixel camera acquires holographic set measurements of all rotating cells that are numerically processed to obtain quantitative two-dimensional phase-contrast maps at different view angles. Accurate numerical algorithms allow to tag each phasecontrast maps with the rotation angle in the microchannel. The couples made of phase-contrast map and measured angle are given as input at tomography algorithms to obtain the refractive index distribution into the cell volume. The approach in principles works properly for any kind of biological matter subjected to rotation as already demonstrated in case of nuclei of plant cells during dehydration. Furthermore, the same approach allows to show the three-dimensional distribution of internalized nano-particles as in case of nano-graphene oxide. The most important achievement and innovation of such strategy is the high-throughput phase-contrast tomography at single cell level that opens to new diagnostic tool thanks to the possibility to have statistically relevant measurement on cell population and also for the possibility to use artificial intelligence architecture for cell identification and classification.
The goal of the SensApp FET-Open project is to develop an innovative super-sensor that will be able to detect Alzheimer’s disease (AD) biomarkers (β-amyloid, Tau and pTAU) in peripheral blood. Considering that nowadays an accurate diagnosis of AD requires the highly invasive withdrawal and analysis of cerebrospinal fluid, SensApp will represent a breakthrough in the field of AD diagnosis thanks to the ability to detect the early stage of the disease by a simple blood collection. We call Droplet-Split-and-Stack (DSS) the new technology that will emerge from SensApp. The achievement of SensApp goal is enabled by the interdisciplinary cooperation between different research institutions and one company involved in the key fields of the project, Vrije Universiteit Brussels, VTT Technical Research Centre of Finland, University of Linz, Ginolis Ltd, IRCCS Centre “Bonino Pulejo”, under the coordination of CNR-Institute of Applied Sciences and Intelligent Systems. This communication will illustrate the progress of the activities.
Nano graphene-based materials offer interesting physicochemical and biological properties for biotechnological applications due to their small size, large surface area and ability to interact with cells/tissues. Among carbon-based nanomaterials, graphene oxide is one of the most used in biological field. There is an increasing interest in shedding light on the interaction mechanisms of nanographene oxide (nGO) with cells. In fact, the effects on human health of GO, and its toxicological profile, are still largely unknown. Here we show that, by minimizing the oxidation degree of GO, its toxicity is significantly reduced in NIH 3T3 cells. Moreover, we show that mild oxidation of graphene nanoplatelets produces nGO particles, which are massively internalized into the cell cytoplasm. MTT(3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) assay was performed to analyze cell viability. Transmission electron microscopy (TEM) analysis was performed to evaluate nGO internalization mechanism into the cytoplasm under different oxidation degree and concentrations. For the first time, we evaluated quantitatively, the cell volume variation after nGO internalization in live fibroblasts through a label-free digital holography (DH) imaging technique and in quasi-real-time modality, thus avoiding the time-consuming and detrimental procedures usually employed by electron-based microscopy. In conclusion, here we have demonstrated that DH can be a viable tool to visualize and display 3D distributions of nano graphene oxide (nGO) uptake by fibroblast cells. DH opens the route for high-throughput investigation at single cell level for understanding how in different conditions nanoparticles aggregates distribute inside the cells.
The effective detection of low-concentrated molecules in small volumes represents a significant challenge in many sectors such as biomedicine, safety, and pollution. Here, we show an easy way to dispense liquid droplets from few μl volume (0.2-0.5 μl) of a mother drop, used as reservoir, by using a pyro-electrohydro-dynamic jetting (p-jet) dispenser. This system is proposed for multi-purpose applications such as printing viscous fluids and as a biosensor system. The p-jet system is based on the pyroelectric effect of polar dielectric crystals such as lithium niobate (LN). The electric field generated by the pyroelectric effect acts electro-hydrodynamically on the sample of liquid, allowing the deposition of small volumes. The p-jet approach allows to obtain the dispensing of drops of very small volumes (up to tenths of a picoliter) avoiding the use of syringes and nozzles generally used in standard technologies. The reliability of the technique as a biosensor is demonstrated both in the case of oligonucleotides and in a sample of clinical interest, namely gliadin. The results show the possibility of detecting these biomolecules even when they are low abundant, i.e. down to attomolar. The results show a marked improvement in the detection limit (LOD) when compared with the conventional technique (ELISA). Moreover, it has been presented the possibility of using the p-jet as a useful tool in the detection of biomarkers, present in the blood but currently not detectable with conventional techniques and related to neurodegenerative diseases such as Alzheimer.
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