Biomedical subjects

Jin-Yu Shao

Publications and source records attributed to Jin-Yu Shao.

10 recordsLinked to original sources

PubMed2006

The adhesion between a microvillus-bearing cell and a ligand-coated substrate: a Monte Carlo study.

In biology, specific cell adhesion is mediated by receptor-ligand interactions. Consequently, its strength correlates with the strength of single receptor-ligand bonds that can be measured with a variety of techniques. However, whether single receptor-ligand bonds are truly present in an experiment is often a concern. In this paper, we present a Monte Carlo simulation of the adhesion between a microvillus-bearing cell and a ligand-coated substrate. In the simulation, ligands were immobilized on the substrate either uniformly or in clusters of three and seven, while receptors were distributed uniformly on the microvillus tip and they moved randomly on the cellular surface. How ligand clustering affects the adhesion frequency and forward rate constant was studied. Other factors that were studied include receptor aggregation on the microvillus tip, ligand density, receptor density, contact time, and binding pocket size. In the case of uniformly distributed ligands, our simulation results agree well with those obtained from probabilistic analysis. We found that, even with clustered ligands on the substrate, most of the adhesion events were mediated by a single bond if the total adhesion frequency was less than 20%. Besides, ligand clustering decreased the total adhesion frequency and forward rate constant, but increased the single-bond adhesion frequency under comparable conditions. These findings should lend us some assistance in identifying single bonds in cell-substrate or cell-bead adhesion measurements and in illustrating some biological mechanisms that involve clustered ligands.

Cell Adhesion↗

PubMed2006

Double-tether extraction from human umbilical vein and dermal microvascular endothelial cells.

Multiple tethers are very likely extracted when leukocytes roll on the endothelium under high shear stress. Endothelial cells have been predicted to contribute more significantly to simultaneous tethers and thus to the overall rolling stabilization. We therefore extracted and quantified double tethers from endothelial cells with the micropipette aspiration technique. We show that the constitutive parameters (threshold force (F0) and effective viscosity (etaeff)) for double-tether extraction are twice those for single-tether extraction and are remarkably similar for human neonatal (F0=105+/-5 pN; etaeff=1.0+/-0.1 pN.s/microm) and adult (F0=118+/-13 pN; etaeff=1.3+/-0.2 pN.s/microm) dermal microvascular, and human umbilical vein (F0=99+/-3 pN; etaeff=1.0+/-0.1 pN.s/microm) endothelial cells. Additionally, these parameters are also independent of surface receptor type, cytokine stimulation, and attachment state of the endothelial cell. We also introduce a novel correlation between the cell-substrate contact stress and gap width, with which we can predict the apparent cell-substrate separation range to be 0.01-0.1 microm during leukocyte rolling. With a biomechanical model of leukocyte rolling, we calculate the force history on the receptor-ligand bond during tether extraction and predict maximum stabilization for the double simultaneous tether extraction case.

Cell Adhesion↗

PubMed2006

Single membrane tether extraction from adult and neonatal dermal microvascular endothelial cells.

Membrane tethers were found to be extracted from leukocytes and macrovascular endothelial cells (e.g., human umbilical vein endothelial cells or HUVECs) when a point pulling force was exerted. These tethers stabilize leukocyte rolling on the endothelium during the inflammatory response. However, little is known about tether extraction from other vascular cells like microvascular endothelial cells (MECs). In this study, we extracted tethers from both adult and neonatal dermal MECs with the micropipette aspiration technique. We found a linear relationship between the pulling force and tether growth velocity for both cell lines. This constitutive relationship is mainly determined by the membrane mechanical property and the underlying actin-based cytoskeleton for both attached and suspended endothelial cells. It is independent of cell surface receptor type, attachment state, cytokine stimulation, or cell lineage. For both types of MECs, the threshold forces are approximately 50 pN and the effective viscosities are around 0.5 pN x s/microm. These results, which are close to what was obtained from HUVECs, indicate that homogeneity is preserved in terms of tether extraction among different types of endothelial cells, and simultaneous tethers are likely extracted when leukocytes roll on either microvascular or macrovascular surfaces.

Adult↗

PubMed2006

Simultaneous tether extraction contributes to neutrophil rolling stabilization: a model study.

Neutrophil rolling is the initial step of neutrophil recruitment to sites of inflammation. During the rolling, membrane tethers are very likely extracted from both the neutrophil and the endothelial cell lining of vessel walls. Here, we present a two-dimensional neutrophil-rolling model to investigate whether and how membrane tethers contribute to stable neutrophil rolling. In our model, neutrophils are assumed to be rigid spheres covered with randomly distributed deformable microvilli, and endothelial cells are modeled as flat membrane surfaces decorated with evenly distributed ligands. The instantaneous rolling velocity and other unknowns of the model are calculated by coupling the hydrodynamic resistance functions, the geometric relationships, and the constitutive equations that govern microvillus extension and tether extraction. Our results show that glutaraldehyde-fixed neutrophils (without microvillus extension or tether extraction) roll unstably on a P-selectin-coated substrate with large variance in rolling velocity. In contrast, normal neutrophils roll much more stably, with small variance in rolling velocity. Compared with tether extraction from the neutrophil alone, simultaneous tether extraction from the neutrophil and endothelial cell greatly increases the lifetime of the adhesive bond that mediates the rolling, allows more transient tethers to make the transition into stable rolling, and enables rolling neutrophils to be more shear-resistant.

Cell Adhesion↗

PubMed2005

A model for CD2/CD58-mediated adhesion strengthening.

Stable cell adhesion is vital for structural integrity and functional efficacy. Yet how low affinity adhesion molecules such as CD2 and CD58 can produce stable cell adhesion is still not completely understood. In this paper, we present a theoretical model that simulates the accumulation of CD2 and CD58 in the contact area of a Jurkat T lymphoblast and a CD58-containing substrate. The cell is assumed to have a spherical shape initially and it is allowed to spread gradually on a circular substrate. Mobile CD2 and CD58 can diffuse freely on both the cell and substrate. Their binding in the contact area is controlled by first-order kinetics. The contact area grows linearly with the total number of CD2/CD58 bonds. Cellular deformation and cytoskeleton involvement were not considered. This time-dependent moving-boundary problem was solved with the Crank-Nicolson finite difference scheme and the variable space grid method. Our simulated results are in reasonable agreement with the experimental observations. The role of diffusion becomes more and more prominent during the contact area increase, which is not sensitive to the kinetic rate constants tested in this study. However, it is very sensitive to the dissociation equilibrium constant and the concentrations of CD2 and CD58.

Adhesiveness↗

PubMed2004

Double tether extraction from human neutrophils and its comparison with CD4+ T-lymphocytes.

The initial arrest and subsequent rolling of a leukocyte on the vascular endothelium is believed to be facilitated by the extraction of tethers, which are narrow membranous tubes drawn from the leukocyte. Although single tether extraction from neutrophils has been studied thoroughly, the relationship between the tether force (F) and tether-growth velocity (U(t)) is still unknown for double tethers drawn from neutrophils. In this study, we have determined this relationship with the micropipette-aspiration technique. As a comparison, tether extraction from CD4+ T-lymphocytes was also studied. The threshold force and effective viscosity for single tether extraction from passive CD4+ T-lymphocytes were found to be 46 pN and 1.55 pN x s/microm, respectively. These values were modulated by stimulation with phorbol myristate acetate (PMA), but not interleukin-8 (IL-8). More importantly, for both types of leukocyte, the threshold force and effective viscosity for double tether extraction are about twice as large as those corresponding to single tether extraction. Neither IL-8 nor PMA stimulation had any effect on this correlation. These results indicate that double tethers are highly localized on cellular surfaces and independent of each other during the rolling process.

CD4-Positive T-Lymphocytes↗

PubMed2004

Quantifying cell-adhesion strength with micropipette manipulation: principle and application.

Quantifying cell-adhesion strength is of great importance in biology and medicine. Cell-adhesion strength can be characterized by separating two adherent cells and determining the force required to do so, or by measuring the lifetime of a receptor-ligand bond that mediates cell adhesion. To this end, several micropipette-based experimental techniques that operate at both cellular and molecular levels have been developed over the past few decades. In this review, we provide an overview of three of these techniques, i.e., the step-pressure technique (SPT), the biomembrane-force probe (BFP), and the micropipette-aspiration technique (MAT). More detailed discussion will be given about the requirements and applications of the MAT.

Biology↗

PubMed2004

Membrane tether extraction from human umbilical vein endothelial cells and its implication in leukocyte rolling.

During the rolling of human neutrophils on the endothelium, tethers (cylindrical membrane tubes) are likely extracted from the neutrophil. Tether extraction reduces the force imposed on the adhesive bond between the neutrophil and endothelium, thereby facilitating the rolling. However, whether tethers can be extracted from the endothelium is still unknown. Here, with the micropipette-aspiration technique, we show that tethers can be extracted from either suspended or attached human umbilical vein endothelial cells. We also show that a linear relationship between the pulling force and tether growth velocity exists and this relationship does not depend on the receptor type (used to impose point forces), tumor necrosis factor-alpha stimulation, or cell attachment state. With linear regression, we determined that the threshold force was 50 pN and the effective viscosity was 0.50 pN.s/microm. Therefore, tethers might be simultaneously extracted from the neutrophil and endothelial cell during the rolling and, more importantly, the endothelial cell might contribute much more to the total composite tether length than the neutrophil. Compared with tether extraction from the neutrophil alone, simultaneous tether extraction results in a larger increase in the lifetime of the adhesive bond, and thus further stabilizes the rolling of neutrophils under high physiological shear stresses.

Cell Adhesion↗

PubMed2002

Finite element analysis of imposing femtonewton forces with micropipette aspiration.

A novel technique of imposing femtonewton forces with micropipette aspiration [i.e., the extended micropipette aspiration technique (EMAT)] is proposed, and an axisymmetric finite element analysis of this technique is provided. The EMAT is experimentally based upon a micropipette manipulation system and is theoretically based upon hydrodynamics. Any spherical object such as a human neutrophil or a latex bead can be employed as the force transducer, so cell-cell interactions can be directly studied. Our computational analysis shows that femtonewton forces can indeed be imposed. The force magnitude is sensitive to the radius of the micropipette and the micropipette-transducer distance, but it is much less sensitive to other parameters including the radius of the transducer, the substrate curvature, and the thickness of the micropipette wall. Combining the EMAT and the previously developed micropipette aspiration technique will allow us to impose an unprecedented range of forces, from a few femtonewtons to a few hundred piconewtons on single molecules or receptor-ligand bonds.

Cell Adhesion↗

PubMed2002

A modified micropipette aspiration technique and its application to tether formation from human neutrophils.

Tether formation, which is mechanically characterized by its threshold force and effective viscosity, is involved in neutrophil emigration from blood circulation. Using the micropipette aspiration technique, which was improved by quantitative contact control and computerized data analysis, we extracted tethers from human neutrophils treated with IL-8, PMA, or cytochalasin D. We found that both IL-8 and PMA elevated the threshold force to about twice as large as the value for passive neutrophils. All these treatments decreased the effective viscosity dramatically (approximately 80%). With a novel method, the residual cortical tension of the cytochalasin-D-treated non-spherical neutrophils was measured to be approximately 8.8 pN/microm.

Cell Membrane↗