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Stefano Guido

Publications and source records attributed to Stefano Guido.

7 recordsLinked to original sources
arXiv2026

Haematocrit and Shear Rate Modulate Local Cell-free Layer Thickness and Platelet Margination in Blood Flow Along a Sinusoidal Wall

The geometry of blood vessels strongly affects hemostasis and thrombosis through red blood cell (RBC) dynamics and platelet margination. Growing platelet aggregates, in turn, reshape the local vessel wall topography, leading to a strongly coupled system. However, it is not well understood how surface heterogeneities alter local hemodynamics and platelet margination, thereby driving further aggregate growth. This study investigates how hematocrit (Ht) and shear rate affect RBC dynamics, cell-free layer (CFL) thickness, and platelet margination near a sinusoidal wall. The sinusoidal wall, with crests and valleys aligned with the flow direction, serves as a model of the flow-aligned platelet aggregates observed in microfluidic experiments [Pero et al., CRPS, 2024]. We perform three-dimensional immersed-boundary-lattice-Boltzmann simulations of particulate blood flow with deformable RBCs and nearly rigid spherical platelets. Our results show that platelet margination is primarily governed by Ht and is more pronounced in regions where the CFL thickness is similar to the platelet size. At low Ht, platelets preferentially accumulate at crests, promoting high-amplitude aggregate growth. Increasing Ht leads to a more uniform platelet distribution along the surface, consistent with experimental observations. The sinusoidal geometry generates a pronounced crest-valley wall shear rate gradient, suggesting that distinct shear-dependent adhesion pathways may dominate at different surface locations. Our findings provide mechanistic insights into the morphological evolution of platelet aggregates and may ultimately inform targeted therapeutic strategies for thrombosis based on shear-sensitive drug-delivery.

physics.flu-dyn↗
arXiv2024

The morphology of cell spheroids in simple shear flow

Cell spheroids are a widely used model to investigate cell-cell and cell-matrix interactions in a 3D microenvironment in vitro. Most research on cell spheroids has been focused on their response to various stimuli under static conditions. Recently, the effect of flow on cell spheroids has been investigated in the context of tumor invasion in interstitial space. In particular, microfluidic perfusion of cell spheroids embedded in a collagen matrix has been shown to modulate cell-cell adhesion and to represent a possible mechanism promoting tumor invasion by interstitial flow. However, studies on the effects of well-defined flow fields on cell spheroids are lacking in the literature. Here, we apply simple shear flow to cell spheroids in a parallel plate apparatus while observing their morphology by optical microscopy. By using image analysis techniques, we show that cell spheroids rotate under flow as rigid particles. As time goes on, cells from the outer layer detach from the sheared cell spheroids and are carried away by the flow. Hence, the size of cell spheroids declines with time at a rate increasing with the external shear stress, which can be used to estimate cell-cell adhesion. The technique proposed in this work allows one to correlate flow-induced effects with microscopy imaging of cell spheroids in a well-established shear flow field, thus providing a method to obtain quantitative results which are relevant in the general field of mechanobiology.

q-bio.CB↗
arXiv2023

A low-cost, user-friendly rheo-optical compression assay to measure mechanical properties of cell spheroids in standard cell culture plates

The mechanical characterization of cell spheroids, one of the most widely used 3D biology models in vitro, is a hotspot of current research on the role played by the mechanical response of cells and tissues. The techniques proposed so far in the literature, while providing important scientific insights, require a specialized equipment and technical skills which are not usually available in cell biology facilities. Here, we present an innovative rheo-optical compression assay based on microscopy glass coverslips as the load applied to cell spheroids in standard cell culture plates and on image acquisition with an optical microscope or even a smartphone equipped with adequate magnification lenses. Mechanical properties can be simply obtained by correlating the applied load to the deformation of cell spheroids measured by image analysis. The low-cost, user-friendly features of the proposed technique can boost mechanobiology research making it easily affordable to any biomedical lab equipped with cell culture facilities.

q-bio.QM↗
arXiv2022

Collective rotational motion of freely-expanding T84 epithelial cell colonies

Coordinated rotational motion is an intriguing, yet still elusive mode of collective cell migration, which is relevant in pathological and morphogenetic processes. Most of the studies on this topic have been carried out on confined epithelial cells. The driver of collective rotation in such conditions has not been clearly elucidated, although it has been speculated that spatial confinement can play an essential role in triggering cell rotation. Here, we study the growth of epithelial cell colonies freely expanding (i.e., with no physical constraints) on the surface of cell culture plates, a case which has received scarce attention in the literature. We find that coordinated cell rotation spontaneously occurs in cell clusters in the free growth regime, thus implying that cell confinement is not necessary to elicit collective rotation as previously suggested. The collective rotation was size and shape dependent: a highly coordinated disk-like rotation was found in small cell clusters with a round shape, while collective rotation was suppressed in large irregular cell clusters generated by merging of different clusters in the course of their growth. The angular motion was persistent in the same direction, although clockwise and anticlockwise rotations were equally likely to occur among different cell clusters. Radial cell velocity was low as compared to the angular velocity. A clear difference in morphology was observed between cells at the periphery and the ones in the core of the clusters, the former being more elongated and spread out as compared to the latter. Overall, our results provide the first quantitative and systematic evidence that coordinated cell rotation does not require a spatial confinement and occurs spontaneously in freely expanding epithelial cell colonies.

cond-mat.soft↗
arXiv2022

Diffusion-induced anisotropic cancer invasion: a novel experimental method based on tumour spheroids

Tumour invasion is strongly influenced by microenvironment and, among other parameters, chemical stimuli play an important role. An innovative methodology for the quantitative investigation of chemotaxis in vitro by live imaging of morphology of cell spheroids, in 3D collagen gel, is presented here. The assay was performed by using a chemotactic chamber to impose a controlled gradients of nutrients (glucose) on spheroids, mimicking the chemotactic stimuli naturally occurring in the proximity of blood vessels. Different tumoral cell lines (PANC-1 and HT-1080) are compared to non-tumoral ones (NIH/3T3). Morphology response is observed by means a Time-lapse workstation equipped with an incubating system and quantified by image analysis techniques. Description of invasion phenomena was based on an engineering approach, based on transport phenomena concepts. As expected, NIH/3T3 spheroids are characterized by a limited tendency of cells to invade the surrounding tissue, unlike PANC-1 and HT-1080 that show relatively stronger response to gradients.

q-bio.CB↗
arXiv2017

Dynamic behaviour of Multilamellar Vesicles under Poiseuille flow

Surfactant solutions exhibit multilamellar surfactant vesicles (MLVs) under flow conditions and in concentration ranges which are found in a large number of industrial applications. MLVs are typically formed from a lamellar phase and play an important role in determining the rheological properties of surfactant solutions. Despite the wide literature on the collective dynamics of flowing MLVs, investigations on the flow behavior of single MLVs are scarce. In this work, we investigate a concentrated aqueous solution of linear alkylbenzene sulfonic acid (HLAS), characterized by MLVs dispersed in an isotropic micellar phase. Rheological tests show that the HLAS solution is a shear-thinning fluid with a power law index dependent on the shear rate. Pressure-driven shear flow of the HLAS solution in glass capillaries is investigated by high-speed video microscopy and image analysis. The so obtained velocity profiles provide evidence of a power-law fluid behaviour of the HLAS solution and images show a flow-focusing effect of the lamellar phase in the central core of the capillary. The flow behavior of individual MLVs shows analogies with that of unilamellar vesicles and emulsion droplets. Deformed MLVs exhibit typical shapes of unilamellar vesicles, such as parachute and bullet-like. Furthermore, MLV velocity follows the classical Hetsroni theory for droplets provided that the power law shear dependent viscosity of the HLAS solution is taken into account. The results of this work are relevant for the processing of surfactant-based systems in which the final properties depend on flow-induced morphology, such as cosmetic formulations and food products.

physics.flu-dyn↗