Lymphocytes are coated with
surface receptors that participate in the
signaling that regulates the
adaptive immune response.
B lymphocytes carry
antibody/
immunoglobulin BCR, while
T lymphocytes carry different
Ig superfamily TCR.
▼
antigen-MHC complex :
BCR :
cascade :
CD3 :
CD4 :
CD8 :
CD45 :
common leukocyte antigen :
co-receptor CD4,
co-receptor CD8 :
cross-linked BCR :
enzymes :
Fc receptors (
FcR) :
IgαIgβ :
immunoreceptor tyrosine-based activation motifs :
intracellular signal :
invariant TCR chain :
ITAMs :
Lck :
leukocyte common antigen :
lymphocyte receptors :
multivalent antigens :
phosphorylation :
phosphorylated ITAMs :
protein kinases :
second messengers :
signal transduction complex - CD3 :
signal transduction molecules :
src-family protein tyrosine kinases (
PTKs) :
Syk :
TCR :
TCR-CDR3 :
TCR diversity :
TCR heterodimers :
TCR-Ig superfamily :
ZAP-70 ▼
Activation of signaling requires
●
lymphocyte receptors, associated with
●
ITAM-bearing
signal transduction molecules, and
●
CD45●
adaptor proteins●
second messengersSignal transduction molecules:
Because both BCR and TCR have very short cytoplasmic
domains they must associate with invariant
signal transduction molecules in order to generate an
intracellular signal (
IgαIgβ for BCR,
CD3 for TCR). The
antigen-specific receptors and signal transduction molecules
cluster together in the
plasma membrane, and signaling is effected by long
ITAM-containing cytoplasmic domains on the signal transduction molecules. ITAMs are
immunoreceptor tyrosine-based activation motifs that are
phosphorylated by
src-family
protein tyrosine kinase enzymes (
PTK).
Protein kinases add phosphate groups to
tyrosine (or
serine or
threonine) residues of
other proteins, often those of
enzymes.
Phosphatases remove the phosphate groups, reversing the effects of protein kinases.
Phospholipases such as PLC cleave specific ester bonds in phosphoglycerides or glycerophosphatidates, converting the phospholipids into fatty acids and other lipophilic substances.
Phospholipase C-γ cleaves the membrane phospholipid,
phosphatidylinositol bisphosphate (PIP2 ) into the signaling molecules,
inositol trisphosphate (
IP3) and
diacylglycerol (
DAG).
Phosphorylation can activate or inactivate enzymes, or can create binding sites that lead to increased concentration of cytoplasmic proteins (and hence
their accessibilty for phosphorylation).
Activation of
lymphocytes also requires
CD45 (
common leukocyte antigen), which is necessory for receptor-mediated activation of lymphocytes.
Phosphorylated ITAMs can bind to
other PTKs (
Syk for B cells,
ZAP-70 for T cells), triggering a
cascade of cytoplasmic enzymes or
second messengers, such as
calcium ions,
diacylglycerol,
G-proteins,
IP3,
MAP kinases,
PKCs, and
transcription factors. Ultimately,
gene expression via
transcription of
mRNA leads to immune activities.
Lymphocyte receptors: BCR and
TCRBCR Heavy chain (H) plus kappa (κ) or lambda (λ) chains.
The surfaces of
B cells are coated with one of thousands of distinct
Ig superfamily receptors,
diversified through
VDJ recombination, which bind to their cognate
antigen at their
antigen-binding site.
Multivalent antigens can
cross-link BCR, generating signals of greater amplitude in
B cells, and potentially
activating the B cells to proliferate and synthesize
IgM in the absence of
T cell-
costimulation. While
B cell activation may be possible without
antigen presentation, B cells are more efficiently activated by binding of BCR to an array of identical
epitopes that are bound to antibody on the
Fc receptors (
FcR) of
macrophages and
neutrophils.
TCRAlpha (α) and beta (β) or gamma (γ) and delta (δ) chains
As
T cells develop in the
thymus, TCR gene segments are
recombined to generate
diverse, unique TCRs. Only those T cells with a TCR
unable to bind self-peptide on self-
MHC leave the
thymus for the periphery.
Antigen-specific receptors on T cells are
not identical to those on B cells (
BCRs). The surface receptors of T cells are members of the
Ig superfamily, with Ig-like domains. Each T cell is coated with a receptor originating in a single
allele, so each receptor binds with a single specificity (
CDR3 for
antigens and CDR1-2 for
MHCs). Clonotypic monoclonal antibodies can recognize TCR idiotypes. Each Ig chain has a variable and a constant region, and CDR of variable regions define the antigen-binding specificity and framework residues.
TCR is a
heterodimer composed usually of α and β chains or, in a minority, γ and δ chains. The two chains are disulfide-bonded exterior to the T cell
plasma membrane in a short extended stretch of amino acids that resembles the
Ig hinge region. TCR, like Ig have very short
cytoplasmic tails. Both TCR chains are glycosylated at sites on their V and C regions.
Each TCR has a single
CDR3 binding site for
antigen, while CDR 1 and CDR 2 bind peptide antigens on
MHC. CDR3 is the most variable. Binding to
CD4 (on helper T cells) or
CD8 (on killer T cells) activates the T cell. Antigen-binding affinity is lower than that of Ig for native (self) antigen, but binding of MHC by the T cell membrane
co-receptors CD4 or CD8 increases the binding affinity of the T cell for the antigen-MHC complex.
TCR expressed on the T cell membrane along with a
signal transduction complex,
CD3, that is called the
invariant TCR chain. CD3 molecules on
all T cells are formed from identical subunits, which are composed of three dimers: gamma epsilon (γε) or delta epsilon (δε), plus either two zetas (ζζ) or a zeta/eta (ζη) heterodimer. The γ and δ chains of CD3 are
not identical to the molecules found in the γd TCR.
CD4 on helper T cells is a monomeric protein with four Ig-like domains, of which the two most distal domains are thought to bind Class II
MHC β2 domain.
CD8 is a disulfide-linked dimer, where the a and β chains each have one Ig-like domain connected by a long extended region to the transmembrane region. CD8 binds to the α3 region of Class I MHC. The cytoplasmic tails of both CD4 and CD8 associate with a
cytoplasmic tyrosine kinase,
Lck, to initiate
signal transduction.
ф
activation ф
affinity maturation ф
anergy ф
antibodies ф
antigen ф
APCs סּ
apoptosis ф
B cells ф
CD סּ
cell-cycle control סּ
cell membranes ф
cellular response סּ
cellular signal transduction ф
class-switch recombination ф
clonal selection ф
complement system ф
costimulation ~
cytokines סּ
GPCRs ф
helper T cell ф
immune response ф
immune tolerance ф
isotype switching ф
killer T cells ф
leukocytes ф
lymphocytes ф
lymphokines ф
macrophages ♦
MAPKs ф
MHC ф
monocytes ф
neutrophils ф
pathogens ф
pattern-recognition receptors ♦
phosphatases ♦
phospholipases ~
phospholipase C-gamma ›››
phosphorylation סּ
phosphotransfer-mediated signaling pathways ♦
PKCs ♦
protein kinases ~
protein tyrosine kinases (
PTKs) ф
receptors סּ
receptor proteins סּ
receptor-mediated endocytosis ♦
receptor tyrosine kinases ф
secondary antibody diversification ~
second messengers ♦
serine/threonine kinases ф
signaling signaling gradients ¤
signaling molecules סּ
signal transduction ф
somatic hypermutation ф
T cells ф
thymus ф
VDJ recombination▲
Top ▲
Tables
Fc receptors
Immune Cytokines
Immunoglobulins
Cell Adhesion Molecules
Cell signaling
Receptor Tyrosine Kinases (RTKs)
Receptor Signal Transduction
Second Messengers
tags
[Immunology] [BCR] [TCR] [ITAM]Labels: ITAM, lymphocytes, signal transduction, surface receptors
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