Presentation 2

Understanding Second
Messengers
Second messengers are small, intracellular molecules that relay signals from cell surface receptors to
trigger diverse cellular responses. They act as crucial intermediaries in the complex process of signal
transduction.
By ARYAN NAGTILAK
Introduction to
Second
Messengers
Second messengers are small, intracellular
molecules that relay signals from cell surface
receptors to .trigger diverse cellular responses.
They act as crucial intermediaries in the
complex process of signal transduction.
By Aryan Nagtilak
Characteristics of Second
Messengers
1. Rapid Activation
Second messengers can be rapidly produced or degraded in response to external stimuli.
2.Amplification
A single receptor activation can generate thousands of second messenger molecules, amplifying
the signal.
3.Specificity
Each second messenger activates a distinct set of target proteins and pathways.
4.Ubiquity
Second messengers are found in a wide range of cell types and organisms.
Types of Second Messengers
Cyclic Nucleotides Calcium (Ca2+) Lipid-derived
Cyclic AMP (cAMP) and cyclic GMP Calcium ion (Ca2+) acts as a ubiquitous Inositol triphosphate (IP3) and
(cGMP) are the most well-studied cyclic second messenger, regulating a variety of diacylglycerol (DAG) are examples of
nucleotide second messengers. cellular processes. lipid-derived second messengers.
Cyclic AMP (cAMP) as a Second Messenger
Cyclic AMP is a cyclic nucleotide, Chemically it is a 3'5' adenosine monophosphate.
It is synthesized in tissues from ATP under influence of ADENYLYL CYCLASE in presence of Mg ion.
It is degraded to 5'AMP by Phosphodiesterase.

Steps of Activation of cAMP pathway
Step1: Binding of ligand to a specific receptor in the cell membrane.
Step2: Activation of G-Protein: after the formation of complex, GDP is replaced by GTP.
Step3: Activation of enzyme

ADENYLATE CYCLASE: activated G-protein either stimulates or inhibits the enzyme adenylate cyclase which is located in plasma
membrane.
Step4: Formation of cAMP: when adenylyl cyclase activated it catalyses the formation of cAMP from cytoplasmic
ATP with Mg2+ as cofactor. Thus a stimulatory G-protein increases the CAMP level whereas inhibitory G protein decreases the cAMP
level.
Step5: Action of cAMP: it activates protein kinase A. PKA then

phosphorylate other proteins which gives rise to cascade of mechanism leads to cell response
Calcium (Ca2+) as a Second Messenger
1)Calcium Release
Activation of some GPCRs leads to the release of calcium from intracellular stores, such as the
endoplasmic reticulum.
2)Calcium Signaling
Increased cytosolic calcium levels can then activate calcium- dependent enzymes and transcription
factors, regulating diverse cellular processes.
3)Calcium Oscillations
Cells can generate complex calcium oscillation patterns, providing a rich, dynamic second messenger signal.
Diacylglycerol (DAG) and Inositol Trisphosphate
(IP3) as Second Messengers
Inositol triphosphate (IP3) is a lipid-derived secondary messenger.
A product of the hydrolysis of the phospholipid phosphatidylinositol 4,5-bisphosphate (PIP2) by the enzyme
phospholipase
Diacylglycerol (DAG) and Inositol Trisphosphate
(IP3) as Second Messengers
Activation
GPCRs leads to the activation of phospholipase C, which cleaves phosphatidylinositol 4,5-bisphosphate (PIP2
DAG and IP3

ates protein kinase C, while IP3 triggers the release of calcium from intracellular stores, leading to diverse cel
3)Crosstalk with Other Pathways

The DAG and IP3 pathways can interact with and modulate other second messenger systems, such
as cAMP and calcium signaling.
Regulation of Second Messenger Pathways
1)Receptor Desensitization
GPCRs can be phosphorylated and internalized, reducing their responsiveness to further stimulation.
2)Feedback Regulation
Second messenger pathways often have built-in negative feedback mechanisms to prevent excessive signalin
3)Crosstalk and Convergence

Second messenger pathways can interact and influence each other, leading to complex, integrated responses.

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Understanding Second

Cyclic Nucleotides Calcium (Ca2+) Lipid-derived

Cyclic AMP is a cyclic nucleotide, Chemically it is a 3'5' adenosine monophosphate.

It is degraded to 5'AMP by Phosphodiesterase.

Step3: Activation of enzyme

Step5: Action of cAMP: it activates protein kinase A. PKA then

Inositol triphosphate (IP3) is a lipid-derived secondary messenger.

DAG and IP3

3)Crosstalk with Other Pathways

3)Crosstalk and Convergence

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