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Ch 3 Day 2 (I)
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Ch 3 Day 2 (I)

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Questions and Answers

Which cellular structure is responsible for proteolytically generating peptide fragments of proteins displayed by class II MHC molecules?

  • Cytosol
  • Late endosomes and lysosomes (correct)
  • Proteasomes
  • Macrophages
  • What type of T cell is activated by the proteasomal processing pathway?

  • B cells
  • Macrophages
  • CD4+ T lymphocytes
  • CD8+ T lymphocytes (correct)
  • From where are the proteins found in late endosomes and lysosomes largely derived?

  • Extracellular environment (correct)
  • Mitochondria
  • Endoplasmic reticulum
  • Cytosol
  • Which pathway ensures that CD4+ T lymphocytes will be able to recognize antigens from microbes originally present outside the APC?

    <p>Endosomal/lysosomal processing pathway</p> Signup and view all the answers

    Which type of cells can present ingested antigens on class I MHC molecules to CD8+ T lymphocytes?

    <p>Dendritic cells</p> Signup and view all the answers

    What happens if peptides weakly bind to class I major histocompatibility complex (MHC) molecules?

    <p>They lead to the degradation of empty MHC molecules</p> Signup and view all the answers

    Which type of T cells recognize Class I MHC-peptide complexes?

    <p>CD8+ T cells</p> Signup and view all the answers

    What is the process called when dendritic cells present ingested antigens on class I MHC molecules to CD8+ T lymphocytes?

    <p>Cross-presentation</p> Signup and view all the answers

    Where are antigenic peptides generated and bound to class I MHC molecules?

    <p>Endoplasmic reticulum</p> Signup and view all the answers

    What is the role of CD4+ helper T cells in the immune response?

    <p>Recognize Class II MHC-peptide complexes</p> Signup and view all the answers

    Which type of antigens can dendritic cells ingest and transport into the cytosol for processing?

    <p>Infected host cells</p> Signup and view all the answers

    Which type of T cells are presented with endocytosed protein antigens in the MHC pathway?

    <p>CD4+ T cells</p> Signup and view all the answers

    Where are antigens destined for presentation via the Class II MHC pathway usually internalized from?

    <p>Extracellular environment</p> Signup and view all the answers

    How are cytosolic proteins tagged for degradation in proteasomes?

    <p>Ubiquitin</p> Signup and view all the answers

    What happens to antigens destined for presentation via the Class II MHC pathway once they are internalized?

    <p>They are degraded in specialized vesicles</p> Signup and view all the answers

    What is the term for the initiation of CD8+ T cell responses to antigens in organ transplants and some intracellular microbes?

    <p>Cross-presentation</p> Signup and view all the answers

    Where do the peptides generated by proteasomes bind to newly synthesized MHC class I molecules?

    <p>ER</p> Signup and view all the answers

    What is the function of tapasin in the MHC class I pathway?

    <p>Association with class I MHC molecules</p> Signup and view all the answers

    How are peptide-MHC complexes recognized by CD4+ helper T cells?

    <p>On the cell surface</p> Signup and view all the answers

    Which molecular pump transports peptides generated by proteasomes into the ER?

    <p>TAP</p> Signup and view all the answers

    What is the function of tapasin in relation to class I MHC molecules?

    <p>Stabilizes peptide binding on MHC molecules</p> Signup and view all the answers

    What stabilizes newly synthesized class I MHC molecules in the ER initially?

    <p>Chaperones</p> Signup and view all the answers

    Which type of T cells recognize peptide-MHC complexes on the cell surface?

    <p>CD8+ T cells</p> Signup and view all the answers

    What is the main function of proteasomes in the MHC pathway?

    <p>Degrade misfolded proteins</p> Signup and view all the answers

    Which mechanism allows for preferential loading of high-affinity peptides onto class I MHC molecules?

    <p>Tapasin interaction</p> Signup and view all the answers

    What is the role of chaperones in the stabilization of class I MHC molecules?

    <p>Stabilization in the ER membrane</p> Signup and view all the answers

    Where are high-affinity peptides preferentially loaded onto class I MHC molecules?

    <p>ER membrane</p> Signup and view all the answers

    Where are Class II MHC molecules synthesized?

    <p>Endoplasmic Reticulum</p> Signup and view all the answers

    What is left in the peptide-binding cleft after the degradation of the invariant chain?

    <p>Class II Invariant Chain Peptide (CLIP)</p> Signup and view all the answers

    Which protein facilitates the exchange of CLIP with other peptides in the vesicles?

    <p>DM</p> Signup and view all the answers

    What type of cells do Class II MHC molecules display peptides to?

    <p>CD4+ T cells</p> Signup and view all the answers

    What type of antigens do Class I MHC molecules bind and display peptides derived from?

    <p>Cytosolic antigens</p> Signup and view all the answers

    Where are extracellular microbes typically captured?

    <p>Phagocytes</p> Signup and view all the answers

    What type of T cells recognize peptides displayed by Class I MHC molecules?

    <p>CD8+ T cells (CTLs)</p> Signup and view all the answers

    Why are T cell-mediated immune responses limited to cell-associated antigens?

    <p>Due to intracellular peptide loading and expression of MHC molecules</p> Signup and view all the answers

    Which compartments facilitate the processing of ingested proteins into peptides?

    <p>Endosomes and lysosomes</p> Signup and view all the answers

    What is the function of CD4+ T cells?

    <p>Activation of an effector mechanism against extracellular microbes</p> Signup and view all the answers

    What is the role of CD8+ T cells?

    <p>Elimination of infected or tumor cells</p> Signup and view all the answers

    Which type of T lymphocytes are responsible for recognizing protein antigens from cytoplasmic microbes?

    <p>CD8+ cytotoxic T lymphocytes</p> Signup and view all the answers

    What pathway do protein antigens from extracellular microbes enter for recognition by T lymphocytes?

    <p>Class II MHC pathway</p> Signup and view all the answers

    What determines the immunodominance of some peptides and the inability of some individuals to respond to certain protein antigens?

    <p>Structural constraints on peptide binding to different MHC molecules</p> Signup and view all the answers

    What is the role of class I MHC pathway in antigen presentation?

    <p>Recognition by CD8+ cytotoxic T lymphocytes</p> Signup and view all the answers

    How do T cells recognize nonpeptide antigens?

    <p>By altering the peptide-binding cleft of MHC molecules</p> Signup and view all the answers

    In some inbred animals, non-expression of certain class II MHC genes led to their inability to respond to:

    <p>Simple protein antigens</p> Signup and view all the answers

    What do protein antigens from cytoplasmic microbes lead to upon recognition by T lymphocytes?

    <p>Killing of infected cells</p> Signup and view all the answers

    What is responsible for displaying peptides of protein antigens for immune response generation?

    <p>Antigen-presenting cells (APCs)</p> Signup and view all the answers

    How are small molecules and metal ions recognized by T cells?

    <p>Through noncovalent binding of chemicals to MHC molecules.</p> Signup and view all the answers

    What is the role of Class II MHC pathway in antigen presentation?

    <p>Recognition by CD4+ helper T lymphocytes.</p> Signup and view all the answers

    What are Major Histocompatibility Complex (MHC) molecules responsible for displaying?

    <p>Peptides of protein antigens.</p> Signup and view all the answers

    Study Notes

    • The text discusses the importance of linking microbes to specific antigen-processing pathways for effective immune response against intracellular and extracellular microbes.
    • Protein antigens from cytoplasmic microbes enter the class I MHC pathway and are recognized by CD8+ cytotoxic T lymphocytes, which kill infected cells.
    • Protein antigens from extracellular microbes enter the class II MHC pathway and are recognized by CD4+ helper T lymphocytes, which activate macrophages to destroy phagocytosed microbes and activate B cells to produce antibodies.
    • Class I MHC pathway: Antigen presentation to cytotoxic T lymphocytes: cytosolic antigen, antigen presentation, binding to CD8+ T cells, and T cell-dependent effector functions.
    • Class II MHC pathway: Antigen presentation to helper T cells: macrophage and extracellular microbe in endosome, binding to CD4+ helper T lymphocytes, release of cytokines, macrophage activation, and B cell antibody secretion.
    • Structural constraints on peptide binding to different MHC molecules determine the immunodominance of some peptides and the inability of some individuals to respond to certain protein antigens.
    • T cells also recognize and react against small molecules and metal ions in an MHC-restricted manner.
    • Some inbred animals did not respond to simple protein antigens due to non-expression of certain class II MHC genes, which were later discovered to be involved in antigen presentation.
    • T cells recognize nonpeptide antigens through covalent modification of self peptides or MHC molecules, or noncovalent binding of chemicals to MHC molecules, altering the peptide-binding cleft and displaying foreign peptide-MHC complexes.
    • The text answers questions about how rare antigen-specific lymphocytes find antigens and generate appropriate immune responses against extracellular and intracellular microbes by explaining the roles of antigen-presenting cells (APCs) and Major Histocompatibility Complex (MHC) molecules in displaying peptides of protein antigens.

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    Test your knowledge about the binding of peptides to class I MHC molecules and their potential to stimulate immune responses. Explore the relationship between peptide binding and the stability of MHC molecules.

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