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Cell Communication Communication Between Cells Yeast Cells Signaling Two mating types • α cells have receptor sites for the a factor and also produce α factor • a cells have receptor sites for the α factor and also produce the a factor. • When mating factors are exchanged, it causes the two cells to fuse and meiosis to occur. 2 Communication Evolved Early When mating factors are exchanged, it causes the two cells to fuse and meiosis to occur. 3 Local Communication Local signaling • Paracrine signaling involves a cell secreting a chemical that induces the differentiation or behavior of nearby target cells. A cell may release a growth factor that may cause surrounding cells to grow and multiply. 4 Neurons Communication • Neurons secrete neurotransmitters that diffuse across an intercellular space (synapse) and interact with another neuron. ** Note - Local signaling in plants is not as well understood because of the plant cell wall, plants must use different mechanisms than those operating in animals. 5 Communication through Direct Contact • Direct contact can occur between cells that have cell junctions. These junctions allow direct contact between the cytoplasm of adjacent cells. • Cell-cell recognition is common in embryonic development and the immune system. 6 Long Distance Signaling Long distance signaling • This involves the use of hormones (a chemical secreted by one cell but exerts it effect on other cells). Animals release hormones into the circulatory system. The hormones travel to target cells. Plants release hormones that travel in their transport system or diffuse into the air as a gas. • Other example: Pheromones 7 Types of Hormones Types of Animal Hormones • Steroid Hormones- For example, testosterone and estrogen • Modified amino acids- For example, thyroxine is a hormone modified from the amino acid tyrosine • Proteins-For example, insulin is a large protein. 8 Stages of Cell Signaling The three stages of cell signaling are: 1. Reception 2. Transduction 3. Response 9 Reception Reception- Begins with the signal (nonsteroid) interacting with a receptor site located on the outside surface of the plasma membrane. The non-steroid signals never enter the cell. When the signal attaches to the receptor, it will cause a change in the shape of the receptor site. Receptors are usually proteins inserted into the plasma membrane. Ligand – a signal triggering molecule that binds to a site on a target protein 10 Types of Membrane Receptors Three major types of membrane receptors are a. G-protein linked receptors b. Tyrosine-kinase receptors c. Ligand-gated ion channels 11 G protein-linked Receptors • G-protein linked receptors vary in their binding sites and recognize and activate different G proteins. • G-proteins are also found in the plasma membrane. 12 G protein-linked Receptors 13 Tyrosine-kinase Receptor • Tyrosine-kinase receptors can activate more than one signaltransduction pathway at one time. This is important when an event like cell reproduction requires multiple pathways to be activated. 14 Tyrosine-kinase Receptor 15 Tyrosine-kinase Receptor 16 Ligand-gated Channels Ligand-gated ion channels are protein pores in a membrane that open or close in response to a chemical signal. This will allow or prevent the flow of ions into or out of the cell (or organelles). Ex. Ca++ channels for muscle contraction and Na+ for neurons 17 Ligand-gated Channels 18 Second Messengers A second messenger is a molecule inside the cell that is needed to trigger the transduction pathway. The most common secondary messengers include: a. cyclic AMP b. Calcium ions and inositol triphosphate (IP3). 19 Cyclic AMP • cAMP is a derivative of ATP. An enzyme, adenylyl cyclase found in the plasma membrane, coverts ATP into cAMP. 20 Cyclic AMP as Second Messenger 21 Calcium Ions Removed from the Cytosol • Most of the time Ca++ in the cytosol is low because it is pumped into the E.R., the mitochondria and also pumped outside of the cell. • When Ca++ ions flood the cytosol, they can be used as second messenger. 22 Ca++ and IP3 used as Second Messengers 23 Ca++ and IP3 used as Second Messengers 24 Transduction • Transduction-This occurs after the reception, the cell needs to process the signal. The biochemical pathway or transduction pathway quite often results in a cascading effect which amplifies each product. • **protein kinases are proteins that transfer phosphate groups from ATP to other proteins 25 Transduction ** Video removed for online classroom Ultimate reason behind signal transduction is that it allows the signal to be amplified. Each step in the pathway can creates many messengers; therefore, one signal molecule can cause the activation of many intracellular molecules (instead of 1 signal molecule causing 1 change in the cell) 26 Cellular Responses (3rd and final stage of signal-transduction pathway) Types of cellular responses 1. Ultimately activating an enzyme. 2. Synthesis of a particular enzyme or protein by activating a gene. • When cAMP, Ca++ or IP3 is activated or made, it is generally followed by interacting with a specific enzyme to start the cascading effect of a particular biochemical pathway. 27 Cellular Responses • Different kinds of cells contain different collections of proteins • These different proteins allow cells to detect and respond to different signals • Even the same signal can have different effects in cells with different proteins and pathways • Pathway branching and “cross-talk” further help the cell coordinate incoming signals 28 Example of Cell Signaling in Plants 29 Role of Scaffolding Proteins • Scaffolding proteins are large relay proteins to which other relay proteins are attached • Scaffolding proteins can increase the signal transduction efficiency by grouping together different proteins involved in the same pathway. 30 Role of Signals that Use Intracellular Receptors (used by steroids) 31