Ch. 3 Antigen Capture and Presentation to Lymphocytes Flashcards
1
Q
MHC restriction
A
an organism’s T-cells can only recognize peptides presented by self-MHC proteins
2
Q
Cross-presentation
A
- DC can take up an antigen from another cell (or a whole other cell) - this would be extracellular
- they can then present this antigen to CD8+ cells via their MHC-1
- normally MHC-1 present intracellular to CD8+
(DC’s can present this same antigen on MHC-II to CD4+ helper cells)
3
Q
MHC - structure, expression
A
- N-terminus is where the peptide binds that is being presented
- they are polymorphic genes for each class, and they are co-dominantly expressed - both are expressed and function regardless of the other one.
4
Q
MHC-I
A
- a1 and a2 bind the antigen - variant domains for diff antigens
- a3 is the invariant domain that binds to CD8 co- receptor (MHC-1 = CD8)
- HLA -A, B, C genes = 6 MHC-1 per person
- Present on all nucleated cells
5
Q
MHC-II
A
- Peptide binds btw variant a1 and B1 regions
- B2 region is the invariant that binds to CD4 co-receptor
- DP, DQ, DR (PQR)
- present on APC - dendritic, macrophages, B-cells
6
Q
molecule that binds inactive MHC-II
A
- invariant chain = CLIP
7
Q
molecule that loads MHC-II with peptide by removing stabilizing molecule
A
DM
8
Q
Processing of MHC-II peptides
A
- Protein taken in f/ extracellular (endocy, phagocy)
- vesicle fuses with lysosome and degrades protein
- phagolysosome fuses with vesicle from ER contain MHC+clip
- DM unloads CLIP from MHC-II
- MHC-II tries to bind with one peptide from the protein (immunodominant epitope - other ones don’t bind the MHC)
- exocytotic vesicle puts MHC-II on the CD4+’s cell surface
9
Q
MHC-I processing
A
- Proteins in the cytoplasm (either from tumor, virus that used cell machinary, or phagocytized protein that escaped vesicle) is ubiquitinated and sent to the proteosome
- proteosome degrades protein into peptides
- peptides are pumped in the ER by TAP
- they are then incorporated to MHC-I and exocytosed into the CD8+ cell surface
10
Q
Molecule that is used in MHC-I transport processing
A
TAP - moves intracellular peptides into the ER where they bind with matching MHC-I complexes
11
Q
2nd signal
A
(first signal is the antigen presented with the self-MHC)
- 2nd signal is needed to stimulate naive T-cells
- it is the co-stimulator B7 that binds CD28 on T-cells
- Microbes induce APC cells to express the co-stimulator and to secrete cytokines to stimulate T-cells
- insures that even if some T-cells will recognize self or harmless non-microbial substances, they won’t respond b/c APC cells won’t be expressing co-stimulators