Fibres of textured biomaterials (BM) enable platelets to adhere with formation of focal contacts. The contact structure and the reaction of the contact associated contractile cytoskeleton were studied using fibres of different flexibility/mobility: butyl-S-Sepharose (S), Polysulfone (PS) and Polyurethane (PU). Ultrastructural and immunocytochemical investigations were carried out to obtain information on the influence of tension on (1) the structure of the focal contacts; (2) the constricting cytoskeleton known to retract adherent collagen or fibrin fibres and (3) the cable-like bundles of actomyosin as observed in the clot. Fibre network from S spheres and 0.3 mm thick frozen sections of PS or PU were incubated with citrated PRP or with washed platelets at 37 C for 6 to 30 min while stirring for contact or activation with ADP or thrombin. Flexible fibres of the BM were found in deep invaginations of the plasmalemma associated with the constricting cytoskeleton. Focal contacts (mediated by fibrinogen as shown immunocytochemically) with fibres which were fixed in the texture or inflexible (PU) induce cable-like bundles of micofilaments containing myosin. These bundles pass across the cytoplasm and connect the contacts with the fibres or with other platelets, as demonstrated by computer-assisted 3-dimensional reconstruction. The model used indicates that retraction is possible as long as fibres are mobile and that cable-like bundles occur when the locomotion of platelets is blocked by immobile fibres. The interaction of platelets with textured BM reflects the situation during collagen or fibrin condensation. The findings may contribute to an understanding of platelet reactions on textured surfaces in grafts.
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http://dx.doi.org/10.3109/09537109409006038 | DOI Listing |
Mechanical forces are critical for virtually all fundamental biological processes, yet quantification of mechanical forces at the molecular scale remains challenging. Here, we present a new strategy using calibrated coiled-coils as genetically encoded, compact, tunable, and modular mechano-sensors to substantially simplify force measurement , via diverse readouts (luminescence, fluorescence and analytical biochemistry) and instrumentation readily available in biology labs. We demonstrate the broad applicability and ease-of-use of these coiled-coil mechano-sensors by measuring forces during cytokinesis (formin Cdc12) and endocytosis (epsin Ent1) in yeast, force distributions in nematode axons (β-spectrin UNC-70), and forces transmitted to the nucleus (mini-nesprin-2G) and within focal adhesions (vinculin) in mammalian cells.
View Article and Find Full Text PDFCell Mol Biol Lett
January 2025
School of Medicine, Shanghai University, Shanghai, 200444, China.
Background: Interfacial heterogeneity is widely explored to reveal molecular mechanisms of force-mediated pathways due to biased tension. However, the influence of cell density,, curvature, and interfacial heterogeneity on underlying pathways of mechanotransduction is obscure.
Methods: Polydimethylsiloxane (PDMS)-based stencils were micropatterned to prepare the micropores for cell culture.
Commun Biol
January 2025
Laboratoire de Chimie Bactérienne (LCB) Institut de Microbiologie, Bioénergies et Biotechnologie (IMM), Aix-Marseille Université-CNRS, UMR 7283, Marseille, France.
Cell movement on surfaces relies on focal adhesion complexes (FAs), which connect cytoskeletal motors to the extracellular matrix to produce traction forces. The soil bacterium Myxococcus xanthus uses a bacterial FA (bFA), for surface movement and predation. The bFA system, known as Agl-Glt, is a complex network of at least 17 proteins spanning the cell envelope.
View Article and Find Full Text PDFCell Signal
January 2025
Division of Bioengineering, Graduate School of Engineering Science, The University of Osaka, Japan; R(3) Institute for Newly-Emerging Science Design, The University of Osaka, Japan; Global Center for Medical Engineering and Informatics, The University of Osaka, Japan. Electronic address:
Aging proceeds with the accumulation of senescent cells in multiple organs. These cells exhibit increased size compared to young cells, which promotes further senescence and age-related diseases. Currently, the molecular mechanism behind the maintenance of such huge cell architecture undergoing senescence remains poorly understood.
View Article and Find Full Text PDFACS Biomater Sci Eng
January 2025
Department of Materials Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8550, Japan.
The structure of many native tissues consists of aligned collagen (Col) fibrils, some of which are further composited with dispersed hydroxyapatite (HAp) nanocrystals. Accurately mimicking this inherent structure is a promising approach to enhance scaffold biocompatibility in tissue engineering. In this study, biomimetic sheets composed of highly aligned Col fibrils were fabricated using a plastic compression and tension method, followed by the deposition of HAp nanocrystals on the surface via an alternate soaking method.
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