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Immunological Synapse 1st Edition by Takashi Saito, Facundo D Batista ISBN 364226185X 9783642261855

  • SKU: BELL-2116108
Immunological Synapse 1st Edition by Takashi Saito, Facundo D Batista ISBN 364226185X 9783642261855
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Immunological Synapse 1st Edition by Takashi Saito, Facundo D Batista ISBN 364226185X 9783642261855 instant download after payment.

Publisher: Springer-Verlag Berlin Heidelberg
File Extension: PDF
File size: 3.05 MB
Pages: 255
Author: Michael L. Dustin (auth.), Takashi Saito, Facundo D. Batista (eds.)
ISBN: 9783642038570, 3642038573
Language: English
Year: 2010
Edition: 1

Product desciption

Immunological Synapse 1st Edition by Takashi Saito, Facundo D Batista ISBN 364226185X 9783642261855 by Michael L. Dustin (auth.), Takashi Saito, Facundo D. Batista (eds.) 9783642038570, 3642038573 instant download after payment.

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Product details:

ISBN 10: 364226185X 
ISBN 13: 9783642261855
Author: Takashi Saito, Facundo D Batista

The proper physiological functioning of most eukaryotic cells requires their assembly into multi-cellular tissues that form organized organ systems. Cells of the immune system develop in bone marrow and lymphoid organs, but as the cells mature they leave these organs and circulate as single cells. Antigen receptors (TCRs) of T cells search for membrane MHC proteins that are bound to peptides derived from infectious pathogens or cellular transformations. The detection of such speci?c peptide–MHC antigens initiates T cell activation, adhesion, and immune-effectors functions. Studies of normal and transformed T cell lines and of T cells from transgenic mice led to comprehensive understanding of the mole- lar basis of antigen-receptor recognition and signaling. In spite of these remarkable genetic and biochemical advances, other key physiological mechanisms that par- cipate in sensing and decoding the immune context to induce the appropriate cellular immune responses remain unresolved. TCRrecognition is tightly regulated to trigger sensitive but balanced T cell responses that result in the effective elimination of the pathogens while minimizing collateral damage to the host. The sensitivity of TCR recognition has to be properly tempered to prevent unintended activation by self-peptide–MHC complexes that cause autoimmune diseases. It is likely that once the TCR is engaged by a peptide– MHC and TCR signaling begins, additional regulatory mechanisms, involving other receptors, would increase the ?delity of the response.

Immunological Synapse 1st Table of contents:

Part I: Foundations and Historical Perspective

  • Chapter 1: Introduction to the Immunological Synapse
    • 1.1 Definition and Early Observations
    • 1.2 The Concept of "Synapse" in Biology (Neuronal vs. Immunological)
    • 1.3 Key Players: T Cells, APCs, NK Cells, B Cells
    • 1.4 Historical Development of the Immunological Synapse Model
    • 1.5 Overview of Functions: Activation, Differentiation, Memory, Cytotoxicity
  • Chapter 2: Core Molecules and Their Initial Interactions
    • 2.1 T Cell Receptor (TCR) Complex: Structure and Ligand Recognition
    • 2.2 Major Histocompatibility Complex (MHC) Molecules (Class I and II)
    • 2.3 Co-stimulatory Molecules (CD28/B7, CD2/LFA-3, LFA-1/ICAM-1)
    • 2.4 Adhesion Molecules and Their Roles in Cell Contact (Integrins, Cadherins)
    • 2.5 Cytokines and Chemokines in Early Recruitment and Signaling

Part II: Formation and Structure of the Immunological Synapse

  • Chapter 3: Dynamics of Synapse Formation
    • 3.1 Initial Cell-Cell Contact and Adhesion
    • 3.2 Receptor-Ligand Binding and Microcluster Formation
    • 3.3 Peripheral Supramolecular Activation Cluster (pSMAC)
    • 3.4 Central Supramolecular Activation Cluster (cSMAC)
    • 3.5 Distinguishing cSMAC from pSMAC: Molecular Composition and Function
    • 3.6 Role of the Cytoskeleton (Actin and Microtubules) in Synapse Reorganization
  • Chapter 4: Molecular Organization of the Synapse
    • 4.1 The Bullseye Model and Its Evolution
    • 4.2 Lipid Rafts and Membrane Microdomains in Synapse Assembly
    • 4.3 Protein-Protein Interactions within Synaptic Microclusters
    • 4.4 Exclusion of Large Molecules (CD45) from the cSMAC
    • 4.5 Force Generation and Mechano-sensing at the Synapse

Part III: Signaling and Functional Outcomes

  • Chapter 5: TCR Signaling Pathways at the Synapse
    • 5.1 Early Signaling Events: Lck, ZAP-70, LAT
    • 5.2 Downstream Signaling Cascades (MAPK, PLCγ1, NFAT, NF-κB)
    • 5.3 Spatiotemporal Control of Signaling within the Synapse
    • 5.4 Negative Regulation of TCR Signaling
  • Chapter 6: Co-stimulation and Co-inhibition at the Synapse
    • 6.1 Integrating Signals from Co-stimulatory Receptors (e.g., CD28, ICOS)
    • 6.2 The Role of Co-inhibitory Receptors (e.g., CTLA-4, PD-1) in Immune Checkpoints
    • 6.3 Fine-Tuning T Cell Activation and Tolerance
  • Chapter 7: Cytokine Secretion and Directed Release
    • 7.1 Polarization of the Secretory Pathway towards the Synapse
    • 7.2 Directed Release of Cytokines (e.g., IL-2, IFN-γ)
    • 7.3 Role of the Golgi Apparatus and Microtubule Organizing Center (MTOC)
  • Chapter 8: Cytotoxic Synapse and Killer Cell Functions
    • 8.1 Formation of the Cytotoxic Synapse by CTLs and NK Cells
    • 8.2 Directed Delivery of Cytotoxic Granules (Perforin, Granzymes)
    • 8.3 Mechanisms of Target Cell Killing (Apoptosis Induction)
    • 8.4 Granzyme Uptake and Mechanisms in Target Cells
    • 8.5 The Role of FasL/Fas Pathway

Part IV: Diverse Immunological Synapses and Their Contexts

  • Chapter 9: B Cell Synapse and Antigen Presentation
    • 9.1 Antigen Recognition by B Cell Receptor (BCR)
    • 9.2 B Cell-T Cell Interaction and Cognate Help
    • 9.3 The B Cell Synapse: Similarities and Differences to T Cell Synapse
    • 9.4 Antigen Extraction and Processing at the B Cell Synapse
  • Chapter 10: Regulatory T Cell (Treg) Synapse
    • 10.1 Mechanisms of Immune Suppression by Tregs
    • 10.2 Molecular Components of the Treg Synapse
    • 10.3 How Tregs Deliver Suppressive Signals to Effector T Cells
  • Chapter 11: Macrophage and Dendritic Cell Synapses
    • 11.1 Interactions of Phagocytes with Lymphocytes
    • 11.2 Formation of Specialized Synapses for Antigen Presentation
    • 11.3 Bidirectional Signaling in Macrophage/DC-T Cell Interactions
  • Chapter 12: Synapses in Vivo: Imaging and Physiological Relevance
    • 12.1 Intravital Microscopy and Live-Cell Imaging of Synapses
    • 12.2 Synapse Formation in Lymphoid Organs (Lymph Nodes, Spleen)
    • 12.3 Role of the Synapse in Immune Surveillance and Disease Pathogenesis

Part V: Clinical Implications and Future Directions

  • Chapter 13: Immunological Synapse in Disease
    • 13.1 Autoimmune Diseases (e.g., Type 1 Diabetes, Rheumatoid Arthritis)
    • 13.2 Cancer Immunotherapy (Targeting Immune Checkpoints)
    • 13.3 Viral Infections and Immune Evasion
    • 13.4 Allergic Reactions and Hypersensitivity
  • Chapter 14: Therapeutic Targeting of the Immunological Synapse
    • 14.1 Modulating Co-stimulatory/Co-inhibitory Pathways
    • 14.2 Engineering T Cells for Adoptive Cell Therapy (CAR T Cells)
    • 14.3 Vaccine Design and Optimizing Immune Responses
    • 14.4 Small Molecule Inhibitors Targeting Synaptic Signaling
  • Chapter 15: Emerging Concepts and Future Technologies
    • 15.1 Beyond the Planar Synapse: 3D Interactions and Niches
    • 15.2 Systems Biology Approaches to Synaptic Signaling
    • 15.3 Single-Cell Resolution Studies of Synapse Formation
    • 15.4 Advances in Imaging Techniques
    • 15.5 Future Challenges and Research Opportunities

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Tags: Takashi Saito, Facundo D Batista, Immunological, Synapse

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