Thrombospondin‐1 Is a Contact Sensor Triggering Adhesion in T Cells and Platelets While Differentially Regulating 2D and 3D Motility in T Cells. Karl‐Gösta Sundqvist

The C-terminal of TSP-1 senses cell contact, which triggers N-terminal cleavage by urokinase, adhesion, and cytoplasmic spreading in T cells and platelets. In contrast, full-length TSP-1 induces the development of polar cell shape and migration in T cells 2D and 3D; polar cell shape 2D, independent of its receptor LRP1, and polar cell shape 3D … Read more

Spatially Resolved Profiling of Compartmentalized Muscle and Brain Inflammation. [[{“value”:”Thorge Dobbertin, Lucas Schirmer”}]]

This review summarizes emerging spatially resolved multi-omics approaches revealing organized cell–cell interactions in skeletal muscle and brain inflammation. These tools uncover radiating molecular programs and niche-specific immunopathology that shape cellular reactivity and vulnerability. ABSTRACT Spatial omics technologies enable high-resolution mapping of transcriptomic, proteomic, and metabolic profiles within intact tissues, revealing how immune, stromal, and parenchymal … Read more

Ccl21a, Rather Than Ccl21b, is Essential for Thymocyte Migration in Mouse. [[{“value”:”Izumi Ohigashi, Hitomi Kyuma, Eri Otsu, Shinichi Hayashi, Tatsuya Takemoto, Yousuke Takahama”}]]

CCR7-mediated chemokine signaling regulates the medullary migration of thymocytes to establish self-tolerance. By comparing the thymic phenotype of Ccl21b-KO mice with that of Ccl21a-KO mice, we show that Ccl21a plays a predominant role compared with Ccl21b among CCR7 ligands in the thymus. ABSTRACT Self-tolerance in T cells is a vital self-defense strategy for mammals to … Read more

CD Molecules Nomenclature 2025: Antibody Validation and Expression Profiling of Immune System G Protein‐Coupled Receptors. [[{“value”:”Javier Fernández‐Calles, Daniela Kužílková, Fanny Hedin, Violeta Bakardjieva‐Mihaylova, Karolina Škvárová Kramarzová, Menno C. van Zelm, Antonio Cosma, Tomas Kalina, Pablo Engel, the Human Cell Differentiation Molecules (HCDM) organization”}]]

HLDA Workshops were established 40 years ago to develop a standardized CD molecule nomenclature for leukocyte cell-surface molecules by comparing monoclonal antibodies (mAbs) produced by different laboratories and companies. The HLDA11 Workshop focused on validating G-protein-coupled receptors (GPCRs) targeting mAbs and assessing cell-type-specific expression patterns in leukocytes. ABSTRACT Monoclonal antibodies (mAbs) targeting cell-surface molecules are … Read more

Serous Cavity Mast Cells Depend on the ROQUIN Paralogs. [[{“value”:”Klaus Heger, Ali Masjedi, Assa Yeroslaviz, Theodor Zeng, Seren Baygün, Angela Vicente‐Luque, Chia‐I. Lien, Lena Osswald, Dieter Saur, Daniel Kovacs, Marc Schmidt‐Supprian”}]]

The RNA-binding ROQUIN paralogs are critical immune regulators. We demonstrate that mast cell-specific deficiency for ROQUIN-1 and ROQUIN-2 in mice leads to loss of mast cells in serous cavities. ROQUIN-1 and 2 ablation does not affect mast cell degranulation or proinflammatory cytokine secretion, although they regulate many mRNAs directly or indirectly. ABSTRACT Mast cells are … Read more

Characterization of the SARS‐CoV‐2‐Specific T Cell Responses in Rheumatoid Arthritis Subjects Vaccinated for COVID‐19 Protection. [[{“value”:”Jaeyoon Song, Ricardo da Silva Antunes, Mehrnaz Agili Seyede, Monica Guma, Alessandro Sette, Alessandra Franco”}]]

SARS-CoV-2 vaccination in rheumatoid arthritis leads to the development of CD4+ and CD8+ spike-specific T cell memory, regardless of immunosuppressive therapies, and the number of vaccine injections. CD4−CD8− double-negative (DN) T cells responded to SARS-CoV-2 peptide epitopes and differentiated into CD8+ cytotoxic T cells after stimulation, suggesting a role in exacerbating the inflammation in RA … Read more

Mastering Immunity: Antibody Feedback as a Driver of Germinal Center Fate and Vaccine Responses. [[{“value”:”Shuang Liu, Yang Zhang, Kai‐Michael Toellner”}]]

Antibody feedback dynamically shapes the selective landscape for GC B-cells, acting as a driving force of Darwinian-like affinity maturation of B-cell receptors (A). It also balances epitope usage, leading to equal competition among B cell clones specific for different epitopes and allowing the emergence of clones specific for new epitopes (B). ABSTRACT Antibody feedback in … Read more

FcµR and IgM‐Mediated Complement Activation Cooperate to Enhance Humoral Immunity. [[{“value”:”Zichao Wen, Lulu Dong, Jun Liu, Qing Min, Ying Wang, Ziying Hu, Xiaoqian Feng, Chaoqun Cui, Yaxuan Li, Yingying Luan, Runyun zhang, Xin Meng, Yue Tang, Hai Zhang, Meiping Yu, Chunhui Lu, Xuzhe Wu, Jingjing Zhao, Jue Wang, Anqi Wang, Birgitta Heyman, Ji‐Yang Wang”}]]

Early B cell activation requires both FcµR and IgM-mediated complement signaling, which together drive initial clonal expansion, class-switch recombination, germinal center (GC) entry, and plasma cell differentiation. During the GC reaction, IgM BCR-mediated complement activation, but not FcµR, supports GC B cell survival, proliferation, and affinity maturation. ABSTRACT Secretory IgM plays a pivotal role in … Read more

Insights Into Complex Murine Models of Allergy and Anaphylaxis: The Central Role of IgE and Mast Cells in Advancing Human Therapies. [[{“value”:”Yuka Nagata, Ryo Suzuki”}]]

Murine allergy model outcomes differ by sensitization route, allergen type, and mouse strain, influencing mechanisms such as IgE and mast cell involvement and the therapeutic relevance of each model. Understanding how experimental parameters shape outcomes is essential for selecting appropriate models and effectively translating findings to clinical applications. ABSTRACT Immunoglobulin E (IgE)–mediated immediate hypersensitivity reactions … Read more

Staphylococcal Enterotoxin A Shapes Monocyte Transcription and Macrophage Polarization: Implications for Immune Responses in Infection and Inflammation. [[{“value”:”Claudia Arasa, Khaleda Rahman Qazi, David Brodin, Manuel Mata Forsberg, Eva Sverremark‐Ekström”}]]

Staphylococcal enterotoxin A (SEA) alters monocyte differentiation and function, while preserving T cell stimulatory capacity. SEA-primed macrophages downregulate antigen-presenting markers yet drive heightened T-cell proliferation and IFN-γ secretion. These findings reveal mechanisms of SEA-mediated immune modulation and superantigen-driven inflammation. ABSTRACT Staphylococcal enterotoxins (SE) crosslink the MHC-II on antigen-presenting cells (APC) with the T-cell receptor, inducing … Read more

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