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Warm-Up 1.Why do you communicate? 2.How do you communicate? 3.How do you think cells communicate? 4.Do you think bacteria can communicate? Explain.

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Warm-Up. Why do you communicate? How do you communicate? How do you think cells communicate? Do you think bacteria can communicate? Explain. Cell Communication. CHAPTER 11. Do bacteria communicate?. Bonnie Bassler on How Bacteria “ Talk ”. Cell Signaling. Animal cells communicate by: - PowerPoint PPT Presentation

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Page 1: Warm-Up

Warm-Up1. Why do you communicate?2. How do you communicate?3. How do you think cells

communicate?4. Do you think bacteria can

communicate? Explain.

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Cell CommunicationCHAPTER 11

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Do bacteria communicate?

Bonnie Bassler on How Bacteria “Talk”

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Cell SignalingAnimal cells communicate

by:Direct contact (gap junctions)Secreting local regulators

(growth factors, neurotransmitters)

Long distance (hormones)

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3 Stages of Cell Signaling:1.Reception: Detection of a signal

molecule (ligand) coming from outside the cell

2.Transduction: Convert signal to a form that can bring about a cellular response

3.Response: Cellular response to the signal molecule

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Reception

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Transduction

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Response

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1. ReceptionBinding between signal molecule (ligand) +

receptor is highly specific.Types of Receptors:

a) Plasma membrane receptor water-soluble ligands

b) Intracellular receptors (cytoplasm, nucleus)

hydrophobic or small ligands Eg. testosterone or nitric oxide (NO)

Ligand binds to receptor protein protein changes SHAPE initiates transduction signal

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Plasma Membrane Receptors

G-Protein Coupled Receptor (GPCR)

Tyrosine Kinase

Ligand-Gated Ion Channels

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G-Protein-Coupled Receptor

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G-Protein-Coupled Receptor

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Plasma Membrane Receptors

G-Protein Coupled Receptor (GPCR)

Tyrosine Kinase

Ligand-Gated Ion Channels

7 transmembrane

segments in membrane

G protein + GTP activates enzyme cell response

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Receptor Tyrosine Kinase

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Plasma Membrane Receptors

G-Protein Coupled Receptor (GPCR)

Tyrosine Kinase

Ligand-Gated Ion Channels

Attaches (P) to tyrosineActivate

multiple cellular responses at

once

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Ligand-Gated Ion Channel

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Plasma Membrane Receptors

G-Protein Coupled Receptor (GPCR)

Tyrosine Kinase

Ligand-Gated Ion Channels

Signal on receptor

changes shapeRegulate flow of

specific ions(Ca2+, Na+)

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2. TransductionCascades of molecular interactions relay

signals from receptors target moleculesProtein kinase: enzyme that

phosphorylates and activates proteins at next level

Phosphorylation cascade: enhance and amplify signal

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Second Messengerssmall, nonprotein molecules/ions that can

relay signal inside cellEg. cyclic AMP (cAMP), calcium ions

(Ca2+), inositol triphosphate (IP3)

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3. Response Regulate protein

synthesis by turning on/off genes in nucleus (gene expression)

Regulate activity of proteins in cytoplasm

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An Example of Cell Communication

http://learn.genetics.utah.edu/content/begin/cells/cellcom/

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Signal transduction pathways can be blocked or defective

Examples:DiabetesCholeraAutoimmune diseaseCancerNeurotoxins, poisons, pesticidesDrugs (anesthetics, antihistamines, blood

pressure meds)

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Cholera

Disease acquired by drinking contaminated water (w/human feces)

Bacteria (Vibrio cholerae) colonizes lining of small intestine and produces toxin

Toxin modifies G-protein involved in regulating salt & water secretion

G protein stuck in active form intestinal cells secrete salts, water

Infected person develops profuse diarrhea and could die from loss of water and salts

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ViagraUsed as treatment for erectile

dysfunctionInhibits hydrolysis of cGMP GMPProlongs signal to relax smooth muscle in

artery walls; increase blood flow to penis

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Apoptosis = cell suicideCell is dismantled and digestedTriggered by signals that activate cascade of

“suicide” proteins (caspase)Why?

Protect neighboring cells from damageAnimal development & maintenance

May be involved in some diseases (Parkinson’s, Alzheimer’s)

Interference may contribute to cancers

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Apoptosis of a human white blood cell

Left: Normal WBCRight: WBC undergoing apoptosis – shrinking and forming lobes (“blebs”)

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Effect of apoptosis during paw development in the mouse