Antigen receptors & signal transduction Flashcards

1
Q

What is a cellular signal?

A

An event that triggers a cell to change its proliferative or activation state.

The receptors need to convert extracellular signals into intracellular biochemical events that result in a cellular response.

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2
Q

The initiation of signaling from a cell surface receptor may require ligand-induced clustering of receptors, called ______-_______, or may involve ________ _____ of the receptor induced by its association with ligand.

A

cross-linking; conformation change

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3
Q

1) What is a common early event in signal transduction?

2) What are the two types of tyrosine kinases?

A

1) A common early event in signal transduction is the PHOSPHORYLATION of a phosphate residue on a TYROSINE (most common in immune cells), serine, or threonine side chain in the cytosolic portion of a receptor or adaptor protein.

2) Non-receptor tyrosine kinases and receptor tyrosine kinases (RTKs)

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4
Q

1) What is the difference between non-receptor tyrosine kinases and receptor tyrosine kinases (RTKs)?

2) Which one is seen on antigen receptors on B and T lymphocytes?

A

1) Non-receptor tyrosine kinases: receptor’s cytosolic tail has no intrinsic catalytic activity so a SEPARATE intracellular tyrosine kinase phosphorylates the receptor or associated protiens.

RTKs: an intrinsic tyrosine kinase domain(s) located in the cytoplasmic tails of the receptors when they are cross-linked by multivalent extracellular ligands.

2) Non-receptor tyrosine kinases

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5
Q

Intracellular signals are often transmitted via multi-protein complexes. Signalling molecules are often composed of distinct domains.

What are the three main signalling protein domains?

A

1) SH2 domains

2) SH3 domains

3) Pleckstrin Homology (PH) domain

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6
Q

Match the signalling protein domains to their definitions:

1) SH2 domains

2) SH3 domains

3) Pleckstrin Homology (PK) domain

A) recognize specific PHOSPHOLIPIDS such as PIP3 found on the inner plasma membrane.

B) composed of 100 amino acids folded in a particular conformation, and they bind to phosphotyrosine containing peptides in certain proteins.

C) composed of 100 amino acids, and they mediate PROTEIN-PROTEIN interactions by binding to PROLINE-rich stretches in certain proteins.

A

SH2 domains: composed of 100 amino acids folded in a particular conformation, and they bind to phosphotyrosine containing peptides in certain proteins.

SH3 domains: composed of 100 amino acids, and they mediate PROTEIN-PROTEIN interactions by binding to PROLINE-rich stretches in certain proteins.

Pleckstrin Homology (PK) domain: recognize specific PHOSPHOLIPIDS such as PIP3 found on the inner plasma membrane.

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7
Q

What are adaptors and scaffolds?

A

Modular proteins used by signalling complexes in lymphocyte activation.

Adaptors/scaffolds function as MOLECULAR HUBS that physically link different enzymes/proteins into a signalling complex so those proteins can interact with each other.

Adaptor/scaffolds LACK ENZYMATIC ACTIVITY.

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8
Q

(T/F) Adaptor is usually bigger than a scaffold.

A

False. Adaptor is usually smaller than a scaffold.

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9
Q

During receptor activation, intracellular signalling proteins are recruited to the plasma membrane.

What are the three ways recruitment is achieved?

A

1) Binding to activated adaptors/scaffold proteins of the membrane

2) Small GTPases

3) Phosphorylation of membrane phospholipids which recruits PH domain containing proteins to the cell membrane

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10
Q

How is recruitment of intracellular signalling proteins to the plasma membrane achieved by binding to activated adaptors/scaffold proteins of the membrane?

A

A typical adaptor protein contains A FEW SPECIFIC DOMAINS that mediate protein-protein interactions. They contain PROLINE-rich stretches that can bind SH3 domains of other proteins and TYROSINE residues that can be phosphorylated for docking sites for other signaling molecules.

Scaffold proteins such as LAT (Linker for the Activation of T cells) are relatively large proteins that can become TYROSINE phosphorylated on multiple sites in order to recruit many different proteins.

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11
Q

Signal transduction can be visualized as a ________ ______ phenomenon.

Why?

A

Social Networking

An initial signal results in proteins being brought close to one another at designated hubs (adaptors), leading the activation of specific enzymes that eventually influence the activation of specific downstream transcription factors or induce other cellular events, such as actin polymerization.

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12
Q

How is recruitment of intracellular signalling proteins to the plasma membrane achieved by small GTPases?

A

Small GTPases exist in two states: GDP bound (inactive) or GTP bound (active). They’re often membrane associated.

GEFs (guanine exchange factors) convert GDP bound to GTP bound.

GEFs are signalling proteins that get recruited to signalling pathways by adaptors such as Grb2 during T cell activation.

SOS (a GEF) activates Ras (a GTPase).

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13
Q

(T/F) Many small GTPases are not membrane-associated.

A

False!

Many are membrane-associated!

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14
Q

How is recruitment of intracellular signalling proteins to the plasma membrane achieved by phosphorylation of membrane phospholipids?

A

The phospholipid, PIP2, is more than a structural phospholipid. It also ACTIVELY PARTICIPATES in CELL SIGNALLING.

PI3 Kinase, when activated during signalling, phosphorylates PIP2 to PIP3 which serves as a binding site for proteins bearing PH domains.

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15
Q

Amplification of intracellular signals can occur via many different mechanisms.

Briefly describe the two common mechanisms of signal amplification.

A

1) Kinase cascades: kinases successively phosphorylate and activate each other in a specific sequence.

2) Generation of small-molecule second messengers: activation of enzymes can produce second messengers which can diffuse throughout the cell and activate specific target proteins. Ca2+ is an example.

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16
Q

Immune receptors are made up of _______ membrane proteins of the ____________ superfamily that are involved in ligand recognition, that associate with other __________ signalling proteins that have unique _________-containing motifs in their cytoplasmic tails.

A

Integral; Immunoglobulin; Transmembrane; Tyrosine

*these tyrosine-containing motifs are the key motifs.

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17
Q

What is the difference between ITAMs and ITIMs?

A

ITAMs: Immunoreceptor Tyrosine-based Activating Motifs. These recruit the Syk/ZAP-70 family TYROSINE KINASE via SH2 domain and induce IMMUNE CELL ACTIVATION.

ITIMs: Immunoreceptor Tyrosine-based Inhibitory Motifs. These induce signalling of inhibiting cellular responses. Phosphorylated ITIMs recruit PHOSPHATASES and counteract ITAM activation.

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18
Q

Which one of the statements is false?

1) Members of the immune receptor family include antigen receptors on B cells and T cells, Fc receptors on myeloid cells and mast cells, and activating and inhibitory receptors on NK cells, T cells, and B cells.

2) B-cell/T cell receptors have very long cytoplasmic domains and thus do not need signalling receptors.

A

2!

B-cell/T cell receptors have very short cytoplasmic domains and thus need signalling receptors to transmit the signal.

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19
Q

There are two tyrosine residues on ITAMs that can be phosphorylated by ______ family kinases when immune receptors are activated.

Tyrosine phosphorylated ITAMs recruit a distinct kinase of the ________ family, which contains two tandem _____ domains that each bind to one of the two phosphorylated motifs on the ITAM.

Binding causes a ________ ____ that activates the kinase, leading to additional signalling events that drive immune cell ________.

A

Src

ZAP-70/Syk; SH2

Conformational change; activation

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20
Q

Briefly list the four features of T and B cell receptor signaling.

A

1) Signaling downstream of T and B cell antigen receptors is characterized by a SIMILAR SEQUENCE of events.

2) The strength of TCR and BCR signaling influence the responses of lymphocytes during their development and activation (weak interactions survive)

3) Antigen receptor signaling is fine-tuned and modulated

4) Antigen receptor signals may cooperate with signals from co-stimulatory receptors.

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21
Q

Signaling downstream of T and B cell antigen receptors is characterized by a SIMILAR SEQUENCE of events.

Describe this sequence of events.

A

1) ligand binding to receptors induce conformational change such as unfolding of the cytoplasmic tail of the receptor that may allow previously hidden tyrosine residues of ITAM motif to become available to be phosphorylated

2) Activated Src family kinase (Lck) phosphorylates tyrosines in the ITAMs of signalling proteins

3) Two phosphorylated tyrosines in a single ITAM are recognized by a Syk family tyrosine kinase (Syk or zap-70) that has tandem SH2 domains that each bind to the phosphotyrosine.

4) Binding of the Syk family kinase causes a conformational change that activates the kinase, leading to additional signalling events that drive immune cell activation.

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22
Q

Antigen receptor signaling is fine-tuned and modulated by a mechanism.

What is the mechanism?

A

Progressive ITAM use!

Different quantities of signal output generated by antigen receptors is translated to the phosphorylation of different numbers of ITAM tyrosines after receptor engagement.

The TCR complex has six signalling chains and ten ITAMs, and increasing number of ITAMs may be phosphorylated with stronger and prolonged binding of antigen to the TCR.

23
Q

(T/F) Co-stimulatory receptors provide first signals for lymphocytes.

A

False!

Co-stimulatory receptors provide second signals for lymphocytes. Antigen recognition provides the first signal.

24
Q

The antigen receptor of T lymphocytes is a
_________ consisting of two transmembrane
polypeptide chains, designated TCR _____ and ____, _______ linked to each other by a _______ bridge between
extracellular cysteine residues.

Both TCR chains have carboxyl-terminal cytoplasmic tails that are ___ to ____ amino acids long.

A

heterodimer; α and β, covalently; disulfide

5; 12 (too short 4 signal transduction thus non-covalently binds to signalling receptors)

25
Q

The TCR complex has six signalling chains and ten ITAMs. What are the chains and where are the ITAMs found?

A

one CD3δ (delta), one CD3γ (gamma), and two CD3ε (epsilon) and two ζ (zeta) chains.

Each CD3 chain has ONE ITAM and each zeta has THREE ITAMs.

26
Q

Briefly answer the following questions regarding the TCR complex:

1) How are the signalling molecules associated with the TCR alpha and beta heterodimer? What signals do they transduce?

2) What are the interactions that occur between the signalling molecules and the TCR heterodimer?

3) Which heterodimer interacts with which signalling molecules?

A

1) The signalling molecules are NON-COVALENTLY associated. When the TCR recognizes antigen, the associated proteins transduce signals that lead to T cell activation.

2) Reciprocal charge interactions between basic and acidic intramembrane amino acids of the subunits. There are two positive charges in the alpha transmembrane region and one in the beta. Negative charges in the signalling transmembrane domains interact with the positive charges.

3) The alpha chain of the TCR interacts with the CD3δ:CD3ε dimer and one ζ dimer. The receptor β chain interacts with one CD3γ:CD3ε and one ζ dimer.

27
Q

What is the immunologic synapse?

What is it also known as?

A

When the TCR complex recognizes MHC-associated peptides on an APC, several T cell surface proteins and intracellular signalling molecules are rapidly MOBILIZED to the SITE OF T cell-APC CONTACT.

The REGION of physical contact between the T cell and the APC forms a bull’s eye like structure that is called the IMMUNOLOGIC synapse, aka SUPRAMOLECULAR ACTIVATION CLUSTER (SMAC).

28
Q

What is the difference between c-SMAC and p-SMAC?

A

c-smac (for CENTER supramolecular activation cluster): it includes the TCR complex, CD4 or CD8 coreceptors, and adaptor proteins associated with the cytoplasmic tails of the transmembrane receptors.

p-SMAC (for PERIPHERAL supramolecular activation cluster): it includes INTEGRINS (such as ICAM-1) that stabilize the binding of the T cell to the APC.

29
Q

(T/F) CD4 and CD8 coreceptors are transmembrane glycoprotein members of the Ig superfamily.

A

True!

30
Q

What is the role of CD4 and CD8 coreceptors in T cell activation?

A

These co-receptors bind to the NON-POLYMORPHIC regions of MHC molecules and trigger signalling by the TCR complex during T cell activation.

Their cytoplasmic tails bind the Src family kinase Lck. During activation, Lck is brought in close proximity to the ITAMs of the TCR complex to phosphorylate both tyrosines. Phosphorylation recruits and activates Zap-70 tyrosine kinase.

This is the first intracellular signal generated once the T cell has recognizes a MHC molecule.

31
Q

(T/F) While the CD4 is expressed as a monomer, CD8 is expressed as heterodimers of alpha and beta chains.

Furthermore, CD8 chains have 4 extracellular Ig domains while CD4 only has one.

A

False!

The CD4 is expressed as a monomer and CD8 is expressed as heterodimers of alpha and beta chains.

However, CD4 has 4 extracellular Ig domains while CD8 chains have one each.

32
Q

During T-cell activation, the phosphorylated ITAMs become a docking site for ZAP-70.

What happens to ZAP-70 following docking on the ITAMs using its two SH2 domains?

A

ZAP-70 gets phosphorylated at specific tyrosine residues by Lck, activating ZAP-70.

Activated ZAP-70 phosphorylates tyrosines on various adaptors and scaffold molecules, such as LAT.

These adaptors become docking sites for cellular enzymes such as PLCγ1 and GEFs for RAS.

33
Q

What are the three major signalling pathways from ZAP-70 phosphorylation?

A

1) Activation RAS –> MAPK pathways –> AP-1

2) Activation PLCγ1 –> IP3 –> NFAT

3) Activation PLCγ1 –> DAG —> NFkB

34
Q

Briefly explain the (Activation RAS –> MAPK pathways –> AP-1) pathway.

A

LAT is phosphorylated by ZAP-70, which then binds the SH2 domains of Grb2.

Grb-2 recruits GEFs called SOS to the plasma membrane, which activates Ras (a small GTPase found on the membrane).

Activated Ras undergoes a conformational change and can then activate a kinase called Raf, the first kinase in the MAP Kinases cascade.

MAP kinase cascade ultimately leads to the transcription of c-Fos, a component of the activation protein 1 (AP-1) transcription factor.

35
Q

How are IP3 and DAG generated?

A

TCR signalling leads to the phosphorylation and activation of PLCy1.

Activated PLCy1 catalyzes the hydrolysis of PIP2 (component of the inner face of eukaryotic plasma membrane) into two breakdown products: double sugar IP3 and membrane bound DAG.

These activate two downstream signalling pathways in T cells.

36
Q

Describe the PLCy1-IP3-mediated signalling; what does it activate and how does it do so?

A

IP3 produces a RAPID INCREASE of cytosolic free calcium within minutes of T cell activation.

Calcium binds to CALMODULIN (regulatory protein). Calcium-calmodulin complex activates several enzymes, including a serine/threonine PHOSPHATASE called CALCINEURIN.

Calcineurin DEPHOSPHORYLATES NFAT (nuclear factor of activated T cells), inducing a conformational change, revealing a NUCLEAR LOCALIZATION SEQUENCE.

Then, NFAT enters nucleus and activates transcription of important T-cell target genes.

37
Q

Inhibitors of calcineurin can act as?

A

effective immunosuppressant and are widely used to prevent rejection of organ transplants.

*T-cell activation is suppressed

38
Q

Describe the PLCy1-DAG-mediated signalling; what does it activate and how does it do so?

A

DAG, a membrane bound lipid, activates certain isoforms of membrane-associated enzyme Protein Kinase C (PKC) by inducing a conformational change.

This change makes the CATALYTIC SITE of the kinase ACCESSIBLE to its substrates.

In T cell activation, PKC-θ localizes to IMMUNOLOGICAL SYNAPSE and is involved in the ACTIVATION and NUCLEAR TRANSLOCATION of Nf-kB.

39
Q

What are the THREE main transcription factors activated by the enzymes generated by TCR signalling?

What do they do?

A

NFAT, AP-1 and NF-kB are the three main TFs.

Binding of the three TFs controls transcriptional regulation of most cytokine genes in T cells.

For example, the IL-2 gene that is important for immune cell proliferation contains binding sites at its promoter for all of these TFs.

40
Q

Match the following TFs to their definitions:

1) NFAT
2) AP-1
3) NF-kB

A) activation involves synthesis of the Fos protein and phosphorylation of preexisting Jun protein, both stimulated by MAP kinases

B) transcription factor that is activated in response to TCR signals and is essential for cytokine synthesis.

C) present in an inactive, serine-phosphorylated form in the cytoplasm of resting T lymphocytes. is activated by the calcium-calmodium-depedent phosphatase calcineurin. activation leads to translocation to the nucelus

A

NFAT: present in an inactive, serine-phosphorylated form in the cytoplasm of resting T lymphocytes. is activated by the calcium-calmodium-depedent phosphatase calcineurin. activation leads to translocation to the nucelus

AP-1: activation involves synthesis of the Fos protein and phosphorylation of preexisting Jun protein, both stimulated by MAP kinases

NF-kB: transcription factor that is activated in response to TCR signals and is essential for cytokine synthesis.

41
Q

(T/F) B cell receptors have long cytoplasmic tails and thus do not need additional signalling molecules.

A

False!

B cell receptors have short cytoplasmic tails that are too small to transduce signals generated after the recognition of antigen.

Ig-mediated signals are transduced by TWO OTHER molecules called Ig alpha and Ig beta that are DISULFIDE linked to one another and NON-COVALENTLY associated with BCR chains.

42
Q

While T cells have 6 different signalling molecules and 10 ITAMs, B cells have ___ signalling chains and ___ ITAM.

A

2 (alpha and beta); 2 ITAMs (one ITAM per chain)

43
Q

Signal initiation by antigens occurs by ________ of the BCR and is facilitated by the ________ for the BCR.

A

Cross-linking; co-receptor

44
Q

What is cross linking in terms of BCR signalling?

What does it do?

A

Cross-linking of membrane Ig by multivalent antigens bring Src family kinases together which get activated through physical interaction, enabling them to phosphorylate the tyrosine residues on the ITAMs of Ig alpha and Ig beta.

Cross-linked Ig receptors enter LIPID RAFTS, where many adaptors proteins and signaling molecules are concentrated.

45
Q

(T/F) After cross-linking of the BCR and the phosphorylation of the ITAMs, the phospho tyrosines provide a docking site for the tandem SH2 domains of the ZAP-70 tyrosine kinase.

A

False!

After cross-linking and the phosphorylation of the ITAMs, the phospho tyrosines provide a docking site for the tandem SH2 domains of the Syk tyrosine kinase.

Like for TCR, Syk is activated when it associates with phosphorylated tyrosines of ITAMs and may itself be phosphorylated on specific tyrosine residues by BCR-associated Src family kinases (like Lck), leading to further activation.

46
Q

Activated Syk phosphorylates tyrosine residues of adaptor or scaffold proteins such as ________.

This recruits enzymes with SH2 containing domains, including ____, ______ and the ___ tyrosine kinase.

A

SLP-65

GEFs; PLCy2; Btk

47
Q

(T/F) The dominant form of PLC is the y1 isoform in B and T cells.

A

False!

The dominant form of PLC is the y2 isoform in B cells, whereas T cells express y2 isoform.

48
Q

How does AP-1 get activated in B cells?

A

SOS is recruited to the adaptor SLP-65 through the binding of the Grb-2 adaptor protein.

Ras becomes activated and activates the ERK MAP kinase pathway.

Rac, another small G protein, activates JNK MAP kinase pathway in similar fashion.

MAP kinase lead to the transcription of AP-1.

49
Q

How does NFAT and Nf-kB get produced in B cells?

A

PLCy2 become active when they bind to SLP-65 and get phosphorylated by Syk and Btk, breaking down PIP2 into IP3 and DAG, leading to activation of NFAT and Nf-kb like in T cells.

50
Q

(T/F) ITAMs are only found in antigen receptors.

A

False!

Receptors other than antigen receptors (NK cells, macrophages, neutrophils, mast cells, basophils) also associate with ITAM-containing chains.

Once their ITAM is phosphorylated, all subsequent process is similar to B and T cells.

51
Q

What are the two common mechanisms of signal termination of immune receptor signalling?

Which one is permanent and which one is reversible?

A

1) Dephosphorylation (reversible)

2) Ubiquitination (permanent)

52
Q

How is termination of intracellular signals done by dephosphorylation?

A

Most but not all inhibitory receptors in the immune system contain ITIM motifs in their cytoplasmic tails that can recruit SH2 domain-containing phosphatases and thus attenuate signalling in a broadly similar manner.

53
Q

How is termination of intracellular signals done by ubiquitination?

A

Enzymes known as E3 ubiquitin ligases induce degradation of certain signalling molecules.

The prototype of E3 ligases involved in terminating T cell responses is CBL-B.

Recruitment of Cbl-b to the TCR complex and associated adaptor proteins leads to the monoubiquitination, endocytosis, and lysosomal degradation of the TCR complex.