Outline Control of src kinase activity by Csk, CD45
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Transcript of Outline Control of src kinase activity by Csk, CD45
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Outline
Control of src kinase activity by Csk, CD45
Control of CD45 activity by dimerization Evidence for TCR/CD3 conformational change zeta, CD3 epsilon; TCR ?
Partial activation and antagonism Lipid rafts and T cell activation Immune synapse or SMAC
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Proximal TCR signaling
1
2
3 3
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The yin and yang of src kinase regulation
SH3 SH2 Y Kinase
P
Y
SH3 SH2 Y Kinase
Csk
Partially Active
Fully Active
Transition
Inactive
SH3 SH2 Y Kinase
P
Y
SH3 SH2
P
Y
Y Kina
seCD45
P
Y
394 in Lck
505 in Lck
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Control of Lckby CD45 and Csk
Lipid Raft
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CD45 isoforms and phosphatase activity
CD45 is a transmembrane phosphatase
Dimerization appears to inhibit activity
There are different size isoforms, created by alternative splicing of exons in the ecto domain
These isoforms have different quantities of glycosylation, which may affect the degree of homo-dimerization
Issue of potential ligand(s) is controversial
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CD45 isoforms
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CD45 isoform expression on B and T cells
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Summary: CD45 isoforms and control of lymphocyte activation
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Initiation of TCR Signaling:
Clustering or Conformation?
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Irving and Weiss expt. demonstrating that crosslinking can be sufficient for T cell activation
CD8 ectoand t.m.
intracellular
transfect intoT cell line
X-link withanti-CD8 Ab
IL-2, etc.
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Models of TCR/CD3 Stoichiometry - Resting State
from: Alarcon et al., EMBO Reports 7:490
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TCR/CD3 Pre-clustering increases
sensitivity to natural
peptide/MHC ligands
from: Alarcon et al., EMBO Reports 7:490
contribution of selfpeptides to activation
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What about a conformational change?
Evidence from GPCR’sfor conformationalchange transmitted
through transmembranedomains to cytoplasm
Structural evidence so far has not demonstrated such
a change in TCR itself
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1 - Evidence for zeta conform. change
zeta assumes folded conformation in the presence of acidic phospholipids at P.M.
phosphorylation frees zeta to assume less-structured conform., whereupon it presumably interacts with effectors
from: Aivazian and Stern, Nat. Struct. Biol. 2000
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2 - Indirect evidence for conformational change in CD3, leading to recruitment of adaptor protein Nck
JNK (MAPK) Activation --> AP-1 transcription
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Inducible binding of Nck to CD3
from: Gil et al., Cell 109:901
Expt. setup: GST fusion with Nck SH3 domain
Pull-downs from lysates of T cells (unstim. or stimulated w/different ab’s - APA 1/1 or APA 1/2)
Blot for CD3
--> Either Ab can crosslink TCR, so difference may be in ability to induce a CD3 conformational change
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from: Gil et al., Cell 109:901
Model from Gil et al. paper
Nck SH3 domain::CD3 proline-rich
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from: Minguet et al., Immunity 26:43
Crosslinking the TCR With a Modified Chain
Thus: the conformational
change in CD3 that allows Nck binding can be induced by clustering TCR/CD3 complexes that are
close to one another
(but w/out a change in TCR
conformation
Antigens for stimulation NIP: hapten
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But…full T cell activation requires both the conformational change and clustering
from: Minguet et al., Immunity 26:43
conform.change
clustering(distant)
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New model: conformation and clustering
from: Minguet et al., Immunity 26:43
pre-formed clusters
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Altered peptide ligands (APL)
analogs of antigenic peptides
usually single amino acid change (TCR contact residue)
antagonists: can inhibit antigenic peptide when mixed
partial agonists: stimulate subset of T cell responses e.g. cytokine release but not proliferation
what properties determine differences?
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Antigenic vs. altered peptides
Kd
On-rateOff-rateStructural changes
CD3,zeta phosphor.Signaling pathwaysTranscription factors
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Lipid rafts
Distribution of lipids in p.m. not uniform
High concentration of sphingolipids and cholesterol in ‘rafts’ - regions of reduced mobility
Proteins with certain lipid modifications partition preferentially to lipid rafts
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Lipid modifications of proteins (acylation)
palmitoylation, myristoylation and prenylation
double acylation (e.g. myrist+palmit or palmit+palmit) leads to lipid raft localization
some src family kinases: myristoylated and palmitoylated
LAT: double palmitoylated
Ras: palmitylated and prenylated
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Lipid rafts and TCR signaling
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Isolation of lipid rafts
Lipid rafts
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Work of Seed and colleagues linking lipid rafts to T cell activation: distribution +/- activation
C: cytoplasmM: membraneD: detergent-insoluble (rafts)
from: Xavier et al., Immunity 8:723
western blot for tyrosine phosphorylation
anti-CD3 Ab
large increase in tyrosinephosphorylation in lipid raftsand recruitment of proteins
to lipid rafts
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LAT palmitylation is required for TCR signaling
from: Lin et al., J Biol Chem 274:28861
Experiment conducted inLAT-deficient T cell line
no lipid raft localization
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Immune Synapse (or SMAC) Model
of Monks and Kupfer
SMAC = supra-molecular activation cluser
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Immunological Synapse and SMAC
ICAM (LFA-1)
MHC/peptide (TCR)
LFA-1 PKC
Live T cells on lipid bi-layersFixed T cell:APC conjugates
from: Grakoui et al., Science 285:221 from: Monks et al., Nature 395:82
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Possible functions for the immune synapse
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But…Signaling can occur in the first few minutes of T cell:APC contact (no mature synapse)
from: Lee et al., Science 295:1539
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Questions about the immunological synapse/SMAC
Is it actually required for early signaling events or more important for later activation? What kind of structures are associated with early signaling?
Is it required for down-regulation of signaling? Internalization of TCR
Recruitment of phosphatases
What cell biological and signaling processes control its formation?