Search Results (406)

As the use of electronics and mobile devices increases, indium and its related compounds are increasingly prevalent in consumer products. However, the effects of the ionic form of indium on the mammalian renal cells are unclear. Understanding indium toxicity in these cells is important, as it relates to kidney health. Kidneys remove heavy metals, maintain electrolyte balance, and perform other vital functions. This in vitro study examines the effects of indium chloride (InCl₃) on Vero cells, focusing on cell morphology, viability, reactive oxygen species (ROS) production, and expression of key focal adhesion proteins. Cells were incubated in culture media with InCl₃ concentrations ranging from 0 to 3.2 mM for 24 h. Fluorescence confocal microscopy analyses revealed that concentrations above 0.8 mM caused the cells to become more compact and display decreased actin filament lengths, suggesting cellular degeneration, which was further supported by the AlamarBlue^® Cell Viability Reagent. Using a 2′,7′–dichlorofluorescin diacetate (DCFDA/H2DCFDA) assay, we show that ROS levels increase with InCl₃ concentration, accompanied by significant increases in focal adhesion kinase (FAK) and paxillin at InCl₃ concentrations above 0.8 mM. Interestingly, the level of α-actinin detected is not affected by exposure to InCl₃. Our findings demonstrate that InCl₃ has negative impacts on the growth and behaviour of Vero cells at concentrations exceeding 0.8 mM, underscoring the need for further investigation into the biological effects of indium-containing compounds. Full article

Neurons achieve their highly polarized architecture by coordinating cytoskeletal systems across space and time, enabling axons to extend over remarkable distances and dendrites to elaborate complex arbours. Early neuroanatomists described intracellular “neurofibrils,” yet these structures remained poorly understood until electron microscopy resolved them into three distinct polymer systems: microtubules, actin filaments, and intermediate filaments. Although this framework clarified neuronal ultrastructure, it simultaneously established a conceptual hierarchy in which microtubules and actin were regarded as the principal drivers of neurite growth, while intermediate filaments were relegated to a passive, supportive role. Unlike prior reviews that document vimentin dynamics primarily from a cell-biological standpoint, this review integrates historical, conceptual, and epistemological perspectives to examine both how and why that hierarchy arose and how it has been dismantled. This review traces how that hierarchy arose and why it has been increasingly reconsidered in favour of intermediate filaments, focusing on vimentin as a case study. Evidence from live cell imaging, molecular manipulation, and genetic models shows that vimentin is dynamically regulated rather than static. Vimentin networks remodel continuously, exchange subunits with soluble pools, and move in coordination with microtubules. Most recently, sparse single-filament labelling combined with correlative volume electron microscopy has demonstrated that individual vimentin filaments remain motile even within dense perinuclear networks previously assumed to be static, a finding that fundamentally redefines what filament density implies about cytoskeletal organization. In neural and neural precursor cells, vimentin expression is developmentally regulated and is prominent during early differentiation stages associated with neurite initiation giving way to neurofilaments in mature neurons. Functional studies further link vimentin to neurite formation and extension, cytoskeletal coordination, organelle positioning, and cellular stress responses. Philosophical analysis reveals that these empirical advances were inseparable from shifts in imaging technology and conceptual framing, and that epistemic risks including model dependency and confirmation bias can be mitigated through methodological pluralism and explicit model disclosure. Taken together, these findings support a revised understanding of intermediate filaments as active, context-dependent contributors to neuronal development and plasticity, and illustrate the value of integrating biological evidence with historical and philosophical reflection. Full article

Dual-material additive manufacturing enables the design of cellular structures with a tailored mechanical response through controlled material distribution and interfacial architecture. In this research, honeycomb structures fabricated by Fused Filament Fabrication (FFF) using dual-material TPU/PLA configurations have been systematically investigated. Particular emphasis is placed on interlocking TPU/PLA joint designs, implemented through tau-shaped and teeth-based geometries, to evaluate their role in load transfer and structural performance. An experimental–analytical model has been developed to characterize the compressive force–displacement response of dual-material honeycombs, capturing the three characteristic deformation regimes—initial stiffness, progressive collapse, and densification—while linking the effective stiffness to the underlying beam-lattice mechanics. The relative contributions of axial and bending deformation mechanisms are quantified through a comparative beam element approach, introducing dimensionless coefficients that reflect the governing deformation mode. The results reveal that the mechanical response is bending-dominated for the examined configurations. The configuration with PLA at the nodes and TPU at the struts exhibits a higher load-carrying capacity and a more stable collapse regime due to a more balanced axial–bending interaction. In contrast, alternative material distributions lead to earlier instability and reduced structural efficiency. The proposed analytical model demonstrates excellent agreement with the experimental data across all configurations. The results demonstrate that properly designed dual-material interlocks can enhance load transfer, decrease stress concentrations, and refine the overall mechanical performance of lightweight cellular structures. Full article

Additive manufacturing (AM) techniques are becoming key factors for repairing and replacing damaged bone. These techniques enable the customization of implants, which can be tailored to the specific area to be treated or healed. Additionally, the combination of absorbable and osteoconductive biomaterials with 3D printing could eliminate second surgeries to remove implants, which is particularly relevant in pediatric and geriatric patients. The capabilities of AM in this context affect not only the external shape but also the internal microarchitecture, where the arrangement of struts to develop complex infills enhances relevant properties such as specific strength, degradation rate, and vascularization. In this study, auxetic scaffold structures made of both polylactic acid (PLA) and a PLA-hydroxyapatite (PLA-HA) composite with 40 wt% of hydroxyapatite (HA) are designed and produced using Fused Filament Fabrication (FFF). Samples of PLA and PLA-HA were 3D printed in dense samples and with auxetic infills. In dense samples, the characterization is performed by X-ray diffraction (XRD), Raman spectroscopy, wettability tests, nanoindentation, and tribological assessments. Two auxetic cellular models have been tested after degradation in PBS media, and their microstructural, structural, and mechanical properties are analyzed. Results show that the addition of hydroxyapatite (HA) significantly improves the hydrophilicity of the PLA matrix, as evidenced by a decrease in water contact angle from 73.4 ± 4.4° to 52.6 ± 2.8° (≈28% reduction), while also enhancing its mechanical and tribological properties, with hardness increasing from 207 ± 30 MPa to 241 ± 28 MPa (≈15%) and Young’s modulus from 4.08 ± 0.55 GPa to 6.24 ± 0.61 GPa (≈53%). Additionally, biodegradation of PLA-HA composites reveals a significant reduction in mechanical properties after 15 days, while the auxetic re-entrant structures mostly retain their shape during compression testing. Full article

Enhancing crop stress tolerance to ensure global food security is one of the core challenges in agricultural science. Plants predominantly face biotic and abiotic stresses, to which they respond by activating finely regulated signal perception and transduction pathways, thereby improving their survival in adverse environments. The plant cytoskeleton, composed of microtubules and actin filaments, plays a pivotal role in this adaptive process. It functions both as a hub for integrating external stress signals and as a key regulator of downstream signaling and cellular responses. Upon stress, the cytoskeleton undergoes dynamic remodeling, a process driven mainly by microtubule-associated proteins (MAPs) and actin-binding proteins (ABPs). This review systematically summarizes current knowledge on cytoskeletal remodeling in plants under environmental stress, particularly focusing on the functions and mechanisms of MAPs and ABPs in cytoskeletal remodeling. Furthermore, it outlines the regulatory network through which the plant cytoskeleton orchestrates stress adaptation. Full article

Ceramidases hydrolyze ceramides to fatty acids and sphingolipids, but their role in fungal response to stress remains unclear. We investigated the function of neutral ceramidase (nCDase) response to aromatic fungicide (carvacrol, cuminaldehyde, and isoniazid) stress in Neurospora crassa. Comparative analysis of the wild-type strain, Δnc and OEnc showed that nCDase enhanced fungicide resistance through multiple mechanisms. nCDase improved β-1,3-glucan synthesis (30% increase), decreased membrane permeability, elevated superoxide dismutase and catalase activities, and promoted carotenoid accumulation (50%), which collectively improved stress tolerance. Δnc exhibited disruption of cellular integrity, altered fatty acid profiles (elevated oleic acid, reduced total fatty acids), and increased fungicide sensitivity. Collectively, these findings established that nCDase as a key regulator of cell wall dynamics, lipid homeostasis, and antioxidant defense, thereby facilitating fungal adaptation to abiotic stress. This study identified the role of nCDase in the response to aromatic fungicide stress and laid foundation for inhibiting pathogenic fungi in agricultural production and food preservation. Full article

Background/Objectives: The rapid emergence of antimicrobial resistance (AMR) is driven not only by antibiotic selective pressure but also by bacterial adaptive responses that enhance genetic diversification under stress. The SOS response, regulated by the RecA-LexA axis, plays a central role in coordinating DNA repair, mutagenesis, and phenotypic adaptation. Targeting this pathway represents a promising strategy to limit bacterial adaptability without directly affecting viability. This study aimed to evaluate benzoxaborole-based compounds as potential inhibitors of the LexA regulatory pathway. Methods: A drug repurposing approach was employed to investigate the benzoxaborole scaffold and the clinically approved derivatives tavaborole and crisaborole. Biochemical assays were used to assess LexA autocleavage in a RecA-dependent co-protease system. Molecular docking analyses were performed to evaluate compound binding within the LexA catalytic site. Microbiological assays were conducted to examine the effects on antibiotic-induced filamentation and biofilm formation under different growth conditions. Results: Selected benzoxaboroles inhibited LexA autocleavage, with tavaborole showing the strongest inhibitory profile in the biochemical assay. Docking analyses supported these findings, indicating stable binding within the LexA catalytic site near the catalytic serine residue. At the cellular level, tavaborole and benzoxaborole significantly reduced levofloxacin-induced filamentation at sub-inhibitory concentrations. Both compounds also decreased biofilm formation under nutrient-limited conditions, while no significant effects were observed on preformed biofilms. Crisaborole showed limited cellular activity despite measurable biochemical effects. Conclusions: These findings identify benzoxaboroles as modulators of the LexA-dependent SOS response and support the potential repurposing of clinically approved compounds as adjuvants to limit bacterial adaptive responses associated with antimicrobial resistance. Full article

Monascus sp. NP1 is a significant filamentous fungus with valuable properties for food industries. Initially isolated from the fermented rice product ang-kak, this strain is known for its ability to produce natural pigments. In this study, we therefore sequenced its genome together with the 26S rRNA D1/D2 domain and ITS fragment for identifying species of Monascus sp. NP1, and further conducted functional annotations of its overall genes related to metabolic capability and growth adaptation using comparative genomics. As a result, promisingly, the NP1 strain was identified as Monascus purpureus with the genome sequences, which was shown to be 23.54 Mb with a GC content of 49.01%. Genome annotation predicted 8031 protein-encoding genes. Comparative genomics between NP1 and 11 other related strains revealed 6024 core groups, 2204 accessory groups, and 5 strain-specific groups. Metabolic pathway analysis promisingly showed carbohydrate metabolism as the most enriched category, particularly central carbon metabolism involving key precursors, e.g., acetyl-CoA and pyruvate that support energy generation and the biosynthesis of pigments, fatty acids, and lipids. These findings highlighted the metabolic versatility and adaptive growth potential of M. purpureus NP1. This study provides key genetic insights into the cellular functions of M. purpureus NP1, laying the groundwork for exploring metabolic properties. It offers a comprehensive understanding for developing targeted applications of M. purpureus NP1 as an alternative fungal cell factory in food and nutrition. Full article

The lateral organization of the plasma membrane (PM) is vital for cellular signaling, yet the specific mechanisms by which the internal cortical actin meshwork templates the organization of the external lipid leaflet remain poorly understood. While established models like the ‘picket-fence’ emphasize physical barriers to diffusion, recent observations of fiber-like “ghost” structures in the distribution of glycosylphosphatidylinositol-anchored proteins (GPI-APs) suggest a more intricate mode of spatial coordination. In this study, we utilize imaging total internal reflection fluorescence correlation spectroscopy (ITIR-FCS) and variable-angle TIRF to resolve whether these filamentous patterns represent genuine membrane-proximal features or optical artifacts of cytosolic transport. Our results demonstrate that these fiber-like tracks are strictly confined to the immediate PM interface and disappear as the evanescent field probes deeper into the cytosol. While the spatial distribution of GPI-APs is templated by the underlying actin meshwork, quantitative diffusion mapping shows that the lateral dynamics of the probe remains largely uniform and is not significantly modulated by these filamentous patterns. By pharmacologically perturbing the actin scaffold and membrane cholesterol, we show that this transbilayer coupling is contingent upon a cholesterol-dependent cytoskeletal pinning mechanism. These findings demonstrate a decoupling of spatial organization and molecular dynamics, providing evidence for how the actin scaffold patterns nanoscale membrane organization without imposing long-range barriers to diffusion. Full article

Small noncoding RNAs play critical regulatory roles in development across organisms. This study profiled microRNAs (miRNAs) and tRNA-derived fragments (tRFs) during bovine conceptus elongation. Elongating conceptuses were obtained via superovulation of eight Angus heifers. Twenty samples from ovoid (OV, n = 6; 0.5–3 mm), tubular (TUB, n = 7; 5–15 mm), and filamentous (FIL, n = 7; 20–34 mm) stages underwent small RNA sequencing. Differential expression of miRNAs and tRFs was analyzed using DESeq2, accounting for donor-sire effects. No tRFs showed differential abundance across any pairwise comparisons. For miRNAs, the expressions of six miRNAs were upregulated in OV versus TUB conceptuses (padj < 0.05), including four let-7 family members (bta-let-7g, bta-let-7f, bta-let-7a-5p, and bta-let-7c) and two additional miRNAs (bta-miR-224 and bta-miR-449a). Furthermore, there were 3 miRNAs differently abundant between the ovoid and filamentous transition (padj < 0.04), including two members of the let7 family (bta-let-7g and bta-let-7f) and bta-miR-449a. Predicted targets of these differentially abundant miRNAs were identified using miRanda. Enrichment analyses of the targeted genes included pathways regulating cellular proliferation, pathways in cancer, and immune-related pathways. The let-7 family, along with miR-449a and miR-224, are candidate regulators of the balance between cellular proliferation and differentiation during elongation, based on their differential abundance and in silico target predictions. Full article

Three-dimensional printed polymers produced using Fused Deposition Modelling (FDM) exhibit directional microstructures resulting from filament paths, layer interfaces, and cellular infill, leading to mechanical and tribological responses distinct from those of homogeneous bulk materials. This study presents a comparative tribomechanical evaluation of polypropylene (PP) bulk inserts and 3D-printed polyethylene terephthalate glycol (PETG) inserts with a 30% hexagonal infill, relevant for robotic gripping applications. Progressive scratch tests were performed under loads from 5 to 100 N (150 N for PP), and profilometry was applied to quantify groove morphology, ridge formation, and displaced-volume ratios. An elasto-plastic conical indentation model was used to derive indentation pressures and elastic–plastic transition radii from groove geometry. The PETG inserts exhibited heterogeneous groove depth, intermittent ridge tearing, and friction fluctuations associated with the internal infill structure, consistent with previous findings on anisotropy and architecture-dependent behaviour in additively manufactured polymers. In contrast, bulk PP demonstrated smoother friction profiles and more stable plastic flow under increasing loads. Two functional indices—specific frictional work and ridge-to-trace volumetric ratio—are introduced to support material selection for robotic gripping systems. The results show that local contact mechanics in 3D-printed inserts are governed by print-induced structural features and can be effectively evaluated through a scratch-based elasto-plastic analysis. The methods and results presented in this work support the rational selection and design of polymer inserts for robotic gripper fingertips. The proposed scratch-based elasto-plastic evaluation framework enables manufacturers and automation engineers to compare 3D-printed and conventional materials based on friction stability, wear response, and deformation resistance. This approach can be directly applied to optimise gripping performance in industrial handling, packaging, and collaborative robotics. Full article

Sandwich structures are increasingly employed in high-performance applications due to their excellent strength-to-weight ratio. However, their mechanical reliability often depends on the structural core, which remains susceptible to failure under shear and flexural loads. Additive manufacturing (AM) enables the design and fabrication of complex, bio-inspired core architectures, such as those derived from Voronoi tessellations, which can potentially enhance energy absorption and mechanical performance. This study investigates the mechanical behavior of PLA-based cellular cores, produced via Fused Filament Fabrication (FFF), under quasi-static and intermediate strain rates (up to 33 s⁻¹). Two infill geometries were compared: a standard cubic pattern and an open Voronoi-based structure inspired by biological morphologies. The results demonstrate strain-rate sensitivity in both configurations, characterized by increased stiffness and peak stress at higher loading rates. While the Voronoi structure exhibited lower maximum strength compared to the cubic pattern, it demonstrated a more gradual post-peak softening, indicating potentially superior energy dissipation capabilities. These findings support the potential of bio-inspired, additively manufactured structures in energy-absorbing applications. Full article

Cadmium (Cd) contamination, through induction of oxidative stress, severely impairs plant growth. Using primary roots of Vicia faba, we investigated how a 24 h incubation in CdCl₂ solution (175 µM) affects mitotic progression in meristems and assessed whether thyme essential oil (TO; 0.03%, v/v), as a natural antioxidant, can protect proliferating cells during simultaneous Cd exposure. Cd strongly inhibited root growth, reduced mitotic index tenfold (to 0.6%), induced chromatin condensation, decreased CDKA protein levels and CycB transcripts and proteins, caused pronounced microtubule bundling and alterations in their arrangement, disorganization of actin filaments, and disturbances in histone H3 phosphorylation (H3T3Ph, H3S10Ph). TO led to a partial recovery of mitotic index (to ~50% of the control), normalization of chromosome condensation, maintenance of cell-cycle regulators at near-control levels, preservation of proper cytoskeletal organization, and restoration of the correct H3 phosphorylation pattern. This enabled cells to progress from metaphase to anaphase and maintain phase proportions close to the control, resulting in normal root growth. These findings indicate that TO protects the mitotic cellular environment against Cd-induced disturbances. To the best of our knowledge, this is the first evidence that TO safeguards the plant mitotic apparatus under Cd stress, highlighting its potential as a natural bioprotective agent supporting plant growth. Full article

Nuclear mechanics and mechanotransduction are involved in the migration and invasion process, such as those in which the cells need to deform themselves to pass through constrictions. Specifically, properties like nuclear softness, viscoelasticity, plasticity (like nuclear pore complexes) and deformability are critical in cancer and its malignant progression. The nucleus represents a physical barrier for the migration and invasion in dense 3D extracellular matrix (ECM) scaffolds. Therefore, the deformability of the nucleus seems to determine the migration limit in circumstances where the enzymatic remodeling of the surroundings is impaired. There are still significant knowledge gaps regarding effects of nuclear deformation during cancer dissemination. It seems that nuclear deformation can alter gene transcription, induce alternative splicing processes, impact nuclear envelope rupture, nuclear pore complex dilatation, damage the DNA, and increase the genomic instability. These mechanically induced alterations can in turn impact the migratory behavior of the cancer cells. The stiffness of the nucleus relies on the condensation of chromatin, and the nuclear lamina, which consists of a network of intermediate filaments underneath the nuclear envelope. All of this is discussed in the review and it is argued that nuclear deformability is universally found in various cancer types. Another focus is placed on the nuclear envelope proteins like emerin, and the SUN-KASH complex and how they contribute to the Linker of Nucleoskeleton and Cytoskeleton (LINC) complex, which consequently couples the nucleus and the cytoskeleton. It is argued that this connection is crucial for force transmission, which governs nuclear stiffness dynamically, depending on the force applied. In this review, recent findings are described that couple ECM-induced nuclear mechanosensing and mechanotransduction with the migration and invasion of cancer cells. Moreover, it is suspected that changes in the mechanosensory characteristics of the cell nucleus could play a pivotal part in the malignancy of cancer cells and the heterogeneity of tumors. Finally, it is discussed what impact the individual elements of the nucleus offer to mechanically alter cellular migration and invasion in cancer and its malignant progression. Full article

Different components of the cytoskeleton are very important determinants of brain development. They orchestrate multiple cellular processes involved in all phases of cerebral cortex development. In this review, we summarize current knowledge on the components of the cytoskeleton—microtubules, actin filaments, and intermediate filaments—and their roles in cortical development. We provide a detailed analysis of how cytoskeleton molecules control neuronal progenitor proliferation, neuronal migration, polarization, axon and dendrite specification and outgrowth, and synaptogenesis. We further examine how pathogenic variants in genes encoding cytoskeletal proteins or their regulators disrupt particular steps of neurogenesis and contribute to major neurodevelopmental disorders (NDDs). Focusing on NDDs such as microcephaly, lissencephaly, corpus callosum agenesis, and synaptopathies, we discuss consequences of cytoskeletal dysfunctions causing altered cellular behavior and clinical phenotypes. By linking molecular defects to developmental and phenotypic consequences, this review highlights the cytoskeleton as a central element in neurodevelopmental pathologies and underscores its potential as a target for future therapeutic strategies. Full article