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1.
Nat Commun ; 14(1): 5644, 2023 09 13.
Article in English | MEDLINE | ID: mdl-37704612

ABSTRACT

To navigate through diverse tissues, migrating cells must balance persistent self-propelled motion with adaptive behaviors to circumvent obstacles. We identify a curvature-sensing mechanism underlying obstacle evasion in immune-like cells. Specifically, we propose that actin polymerization at the advancing edge of migrating cells is inhibited by the curvature-sensitive BAR domain protein Snx33 in regions with inward plasma membrane curvature. The genetic perturbation of this machinery reduces the cells' capacity to evade obstructions combined with faster and more persistent cell migration in obstacle-free environments. Our results show how cells can read out their surface topography and utilize actin and plasma membrane biophysics to interpret their environment, allowing them to adaptively decide if they should move ahead or turn away. On the basis of our findings, we propose that the natural diversity of BAR domain proteins may allow cells to tune their curvature sensing machinery to match the shape characteristics in their environment.


Subject(s)
Actins , Adaptation, Psychological , Cell Membrane , Cell Movement , Biophysics
2.
Nat Commun ; 11(1): 147, 2020 01 09.
Article in English | MEDLINE | ID: mdl-31919342

ABSTRACT

During HIV infection, cell-to-cell transmission results in endosomal uptake of the virus by target CD4+ T cells and potential exposure of the viral ssRNA genome to endosomal Toll-like receptors (TLRs). TLRs are instrumental in activating inflammatory responses in innate immune cells, but their function in adaptive immune cells is less well understood. Here we show that synthetic ligands of TLR8 boosted T cell receptor signaling, resulting in increased cytokine production and upregulation of surface activation markers. Adjuvant TLR8 stimulation, but not TLR7 or TLR9, further promoted T helper cell differentiation towards Th1 and Th17. In addition, we found that endosomal HIV induced cytokine secretion from CD4+ T cells in a TLR8-specific manner. TLR8 engagement also enhanced HIV-1 replication and potentiated the reversal of latency in patient-derived T cells. The adjuvant TLR8 activity in T cells can contribute to viral dissemination in the lymph node and low-grade inflammation in HIV patients. In addition, it can potentially be exploited for therapeutic targeting and vaccine development.


Subject(s)
HIV Infections/immunology , HIV-1/immunology , Th1 Cells/immunology , Th17 Cells/immunology , Toll-Like Receptor 8/metabolism , Cell Line , HIV Infections/transmission , Humans , Immunity, Innate/immunology , Signal Transduction/immunology , Toll-Like Receptor 8/immunology
3.
PLoS One ; 10(9): e0134644, 2015.
Article in English | MEDLINE | ID: mdl-26406896

ABSTRACT

Mycobacteria pose a threat to the world health today, with pathogenic and opportunistic bacteria causing tuberculosis and non-tuberculous disease in large parts of the population. Much is still unknown about the interplay between bacteria and host during infection and disease, and more research is needed to meet the challenge of drug resistance and inefficient vaccines. This work establishes a reliable and reproducible method for performing correlative imaging of human macrophages infected with mycobacteria at an ultra-high resolution and in 3D. Focused Ion Beam/Scanning Electron Microscopy (FIB/SEM) tomography is applied, together with confocal fluorescence microscopy for localization of appropriately infected cells. The method is based on an Aclar poly(chloro-tri-fluoro)ethylene substrate, micropatterned into an advantageous geometry by a simple thermomoulding process. The platform increases the throughput and quality of FIB/SEM tomography analyses, and was successfully applied to detail the intracellular environment of a whole mycobacterium-infected macrophage in 3D.


Subject(s)
Imaging, Three-Dimensional , Leukocytes, Mononuclear/microbiology , Leukocytes, Mononuclear/pathology , Mycobacterium , Electron Microscope Tomography , Humans , Image Processing, Computer-Assisted , Leukocytes, Mononuclear/ultrastructure , Macrophages/microbiology , Macrophages/pathology , Macrophages/ultrastructure , Microscopy, Confocal , Microscopy, Electron, Scanning , Mycobacterium/physiology
4.
PLoS One ; 9(3): e91662, 2014.
Article in English | MEDLINE | ID: mdl-24626259

ABSTRACT

A popular approach to make neocartilage in vitro is to immobilize cells with chondrogenic potential in hydrogels. However, functional cartilage cannot be obtained by control of cells only, as function of cartilage is largely dictated by architecture of extracellular matrix (ECM). Therefore, characterization of the cells, coupled with structural and biochemical characterization of ECM, is essential in understanding neocartilage assembly to create functional implants in vitro. We focused on mesenchymal stem cells (MSC) immobilized in alginate hydrogels, and used immunohistochemistry (IHC) and gene expression analysis combined with advanced microscopy techniques to describe properties of cells and distribution and organization of the forming ECM. In particular, we used second harmonic generation (SHG) microscopy and focused ion beam/scanning electron microscopy (FIB/SEM) to study distribution and assembly of collagen. Samples with low cell seeding density (1e7 MSC/ml) showed type II collagen molecules distributed evenly through the hydrogel. However, SHG microscopy clearly indicated only pericellular localization of assembled fibrils. Their distribution was improved in hydrogels seeded with 5e7 MSC/ml. In those samples, FIB/SEM with nm resolution was used to visualize distribution of collagen fibrils in a three dimensional network extending from the pericellular region into the ECM. In addition, distribution of enzymes involved in procollagen processing were investigated in the alginate hydrogel by IHC. It was discovered that, at high cell seeding density, procollagen processing and fibril assembly was also occurring far away from the cell surface, indicating sufficient transport of procollagen and enzymes in the intercellular space. At lower cell seeding density, the concentration of enzymes involved in procollagen processing was presumably too low. FIB/SEM and SHG microscopy combined with IHC localization of specific proteins were shown to provide meaningful insight into ECM assembly of neocartilage, which will lead to better understanding of cartilage formation and development of new tissue engineering strategies.


Subject(s)
Alginates/chemistry , Cartilage/pathology , Cell Culture Techniques , Hydrogels/chemistry , Mesenchymal Stem Cells/cytology , ADAM Proteins/metabolism , ADAMTS Proteins , Cartilage, Articular/pathology , Cell Differentiation , Chondrocytes/cytology , Chondrogenesis , Collagen/chemistry , Extracellular Matrix/chemistry , Gene Expression Regulation , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Humans , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Immunohistochemistry , Models, Theoretical , Procollagen N-Endopeptidase/metabolism , Tissue Engineering/methods
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