Lecture 1: Cell Signaling & Cell-Cell communication
PART I: Cell Signaling
Cell signaling encompasses:
- Cell-cell communication
- Sensing and interacting with the extracellular
environment
- Sensing and responding to changes in the
intracellular environment
A) Contact-dependent
- Short distance
- Direct cell-to-cell contact
- Important in embryonic
development and
immune responses
B) Paracrine
- Short distance (without
contact)
- Secreted signal
molecules
- Modulate response in
nearby cells
- Important in inflammation
response
C) Synaptic
- Long distance
- Fast (action potential
travels with 100m/s)
- Neurotransmitters
- Regulated exocytosis into the synaptic cleft
D) Endocrine
- Long range, broad
- Signal molecules: hormones
- Secretion into the bloodstream
- E.g., insulin, adrenaline
Extracellular signal molecules:
- Chemical (e.g. nutrient, hormones, odors, DNA/RNA)
- Physical cues (e.g.) pressure, temperature, light)
,Cell Surface Receptors → Large, hydrophilic signal molecules
- Ion-channels coupled receptors
- G-protein coupled receptors (GPCRs)
- Enzyme-coupled receptors (e.g. receptor tyrosine kinases)
Intracellular receptors → Small hydrophobic molecules (e.g. steroids, gasses)
- Nuclear receptors (directly activating transcription factors)
Not all receptors are localized on the cell surface
Large, hydrophilic signal molecules Small, hydrophobic molecules (e.g. steroids, gasses)
The same input can create distinct responses in different cell types
For example: acetylcholine
a) Same receptor
i) Heart pacemaker cell → decreased rate of firing
ii) Salivary gland cell → secretion
b) Different receptor
i) Skeletal muscle → contraction
Signaling networks are often highly complex
Signalling responses can be fast or slow
- Fast (less than a second to minute) → most likely
altered protein function
- Slow (minutes to hours) → Altered gene expression
Breaking large networks down, creates
signaling motifs
Not all receptors are localized on the cell
surface
- Large, hydrophilic signal molecules;
cannot cross plasma membrane do
cell surface receptors
, - Small, hydrophobic molecules (e.g. steroid, gases); can pass the plasma membrane so
intracellular receptors
Regulation of signaling proteins (molecular switches)
● Binding-mediated regulation
○ Ligand binding
■ Ion-channel-coupled receptors
■ G-protein-coupled receptors (GPCRs)
■ Enzyme-coupled receptors
○ Protein binding
● Enzymatic regulation
○ GTP hydrolysis (GTP binding proteins)
○ Post-translational modifications
Ion-channel coupled receptors
● Ligands
○ Neurotransmitters → acetylcholine, glycine,
glutamate, GABA
○ Second messenger → inositol-1,4,5-triphosphate, Ca2+
● Structure
○ Heterogenous family of multipass
transmembrane proteins
○ Often with several subunits
● Mode of action
○ Ligand-binding induces opening or closing of the channel
to regulate ion influx / outflux
→ Example: skeletal muscle acetylcholine receptor (motor end
plate, neuromuscular junction)
G-protein-coupled receptors (GPCRs)
● Ligands:
○ Neurotransmitters
○ Proteins
○ Peptides
○ Hormones
○ Derivatives of amino acids and fatty
acids
● Structure
○ Single polypeptide chain
○ 7 transmembrane helices
● Mode of action
○ Ligand-binding induces conformational
change in the intracellular domain
, ○ Associate and regulate the activity of intracellular heterotrimeric G proteins
● Importance:
○ > 35% of all approved pharmaceuticals target GPCRs (including cannabinoids
and opioids)
→ Example: Angiotensin II type 1 - AT1 receptor (mediates constriction of blood vessels)
Enzyme-coupled receptors
● Receptor Tyrosine Kinases (RTKs) / Cytokine
receptors
○ Ligands
■ Mainly signal protein ligands (e.g.
insulin, growth factors, cytokines)
○ Structures
■ Typically single pass membrane domain
■ Directly encode or are tightly associated with an intracellular kinase
○ Mode of action
■ Ligand-binding induces dimerization
■ Dimerization leads to the inter- and intramolecular phosphorylation of the
receptor
■ Phosphorylated receptors act as scaffold to recruit additional proteins
Receptor tyrosine kinases (RTKs) Cytokine receptor
Binding-mediated regulation
1) Ligand binding
a) Second messengers: small signaling
molecules release by the cell in response
to receptor activation in order to mediate
the intracellular response
i) Hydrophilic second messengers:
(1) CA2+, cAMP, cGMP, IP3
ii) Hydrophobic second messengers
(1) Diacylglycerol, phosphatidylinositol
iii) Examples:
→ Ca2+ binds and activated calmodulin
- Activated ca2+/Calmodulin-dependent kinase (CamKII,
transcriptional regulation)
PART I: Cell Signaling
Cell signaling encompasses:
- Cell-cell communication
- Sensing and interacting with the extracellular
environment
- Sensing and responding to changes in the
intracellular environment
A) Contact-dependent
- Short distance
- Direct cell-to-cell contact
- Important in embryonic
development and
immune responses
B) Paracrine
- Short distance (without
contact)
- Secreted signal
molecules
- Modulate response in
nearby cells
- Important in inflammation
response
C) Synaptic
- Long distance
- Fast (action potential
travels with 100m/s)
- Neurotransmitters
- Regulated exocytosis into the synaptic cleft
D) Endocrine
- Long range, broad
- Signal molecules: hormones
- Secretion into the bloodstream
- E.g., insulin, adrenaline
Extracellular signal molecules:
- Chemical (e.g. nutrient, hormones, odors, DNA/RNA)
- Physical cues (e.g.) pressure, temperature, light)
,Cell Surface Receptors → Large, hydrophilic signal molecules
- Ion-channels coupled receptors
- G-protein coupled receptors (GPCRs)
- Enzyme-coupled receptors (e.g. receptor tyrosine kinases)
Intracellular receptors → Small hydrophobic molecules (e.g. steroids, gasses)
- Nuclear receptors (directly activating transcription factors)
Not all receptors are localized on the cell surface
Large, hydrophilic signal molecules Small, hydrophobic molecules (e.g. steroids, gasses)
The same input can create distinct responses in different cell types
For example: acetylcholine
a) Same receptor
i) Heart pacemaker cell → decreased rate of firing
ii) Salivary gland cell → secretion
b) Different receptor
i) Skeletal muscle → contraction
Signaling networks are often highly complex
Signalling responses can be fast or slow
- Fast (less than a second to minute) → most likely
altered protein function
- Slow (minutes to hours) → Altered gene expression
Breaking large networks down, creates
signaling motifs
Not all receptors are localized on the cell
surface
- Large, hydrophilic signal molecules;
cannot cross plasma membrane do
cell surface receptors
, - Small, hydrophobic molecules (e.g. steroid, gases); can pass the plasma membrane so
intracellular receptors
Regulation of signaling proteins (molecular switches)
● Binding-mediated regulation
○ Ligand binding
■ Ion-channel-coupled receptors
■ G-protein-coupled receptors (GPCRs)
■ Enzyme-coupled receptors
○ Protein binding
● Enzymatic regulation
○ GTP hydrolysis (GTP binding proteins)
○ Post-translational modifications
Ion-channel coupled receptors
● Ligands
○ Neurotransmitters → acetylcholine, glycine,
glutamate, GABA
○ Second messenger → inositol-1,4,5-triphosphate, Ca2+
● Structure
○ Heterogenous family of multipass
transmembrane proteins
○ Often with several subunits
● Mode of action
○ Ligand-binding induces opening or closing of the channel
to regulate ion influx / outflux
→ Example: skeletal muscle acetylcholine receptor (motor end
plate, neuromuscular junction)
G-protein-coupled receptors (GPCRs)
● Ligands:
○ Neurotransmitters
○ Proteins
○ Peptides
○ Hormones
○ Derivatives of amino acids and fatty
acids
● Structure
○ Single polypeptide chain
○ 7 transmembrane helices
● Mode of action
○ Ligand-binding induces conformational
change in the intracellular domain
, ○ Associate and regulate the activity of intracellular heterotrimeric G proteins
● Importance:
○ > 35% of all approved pharmaceuticals target GPCRs (including cannabinoids
and opioids)
→ Example: Angiotensin II type 1 - AT1 receptor (mediates constriction of blood vessels)
Enzyme-coupled receptors
● Receptor Tyrosine Kinases (RTKs) / Cytokine
receptors
○ Ligands
■ Mainly signal protein ligands (e.g.
insulin, growth factors, cytokines)
○ Structures
■ Typically single pass membrane domain
■ Directly encode or are tightly associated with an intracellular kinase
○ Mode of action
■ Ligand-binding induces dimerization
■ Dimerization leads to the inter- and intramolecular phosphorylation of the
receptor
■ Phosphorylated receptors act as scaffold to recruit additional proteins
Receptor tyrosine kinases (RTKs) Cytokine receptor
Binding-mediated regulation
1) Ligand binding
a) Second messengers: small signaling
molecules release by the cell in response
to receptor activation in order to mediate
the intracellular response
i) Hydrophilic second messengers:
(1) CA2+, cAMP, cGMP, IP3
ii) Hydrophobic second messengers
(1) Diacylglycerol, phosphatidylinositol
iii) Examples:
→ Ca2+ binds and activated calmodulin
- Activated ca2+/Calmodulin-dependent kinase (CamKII,
transcriptional regulation)