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The Importance of Cells
• All organisms are made of cells•The cell is the simplest collection of matter
that can live•Cell structure is correlated to cellular
function•All cells are related by their descent from
earlier cells
Microscopy•light microscope (LM)
▫visible light passes through a specimen and then through glass lenses, which magnify the image
▫Magnify up to 1000x
LE 6-2
Measurements1 centimeter (cm) = 10–2 meter (m) = 0.4 inch1 millimeter (mm) = 10–3 m1 micrometer (µm) = 10–3 mm = 10–6 m1 nanometer (nm) = 10–3 µm = 10–9 m
10 m
1 mHuman height
Length of somenerve andmuscle cells
Chicken egg
0.1 m
1 cm
Frog egg1 mm
100 µm
Most plant andanimal cells
10 µmNucleus
1 µm
Most bacteria
Mitochondrion
Smallest bacteria
Viruses100 nm
10 nmRibosomes
Proteins
Lipids
1 nmSmall molecules
Atoms0.1 nmU
na
ide
d e
ye
Lig
ht
mic
rosc
op
e
Ele
ctr
on
mic
ros
co
pe
•electron microscopes (EMs)▫ are used to study subcellular structures ▫Two types
Scanning electron microscopes (SEMs) focus a beam of electrons onto the surface of a
specimen providing images that look 3D
Transmission electron microscopes (TEMs) focus a beam of electrons through a specimen to study the internal structures of cells
LE 6-41 µm
1 µm
Scanning electronmicroscopy (SEM) Cilia
Longitudinalsection ofcilium
Transmission electronmicroscopy (TEM)
Cross sectionof cilium
•Basic features of all cells: ▫Plasma membrane
Selectively permeable double layer of phospholipids
▫Semifluid substance called the cytosol Includes cytoplasm & organelles
▫Chromosomes (carry genes)▫Ribosomes (make proteins)
LE 6-8
Hydrophilicregion
Hydrophobicregion
Carbohydrate side chain
Structure of the plasma membrane
Hydrophilicregion
Phospholipid Proteins
Outside of cell
Inside of cell 0.1 µm
TEM of a plasma membrane
Prokaryotic Cells Eukaryotic Cells
•no nucleus•DNA is in an
unbound region called the nucleoid
•No membrane-bound organelles
•Include bacteria and Achaea
• Have nucleus• DNA in nucleus• Membrane-bound
organelles• Usually larger than
prokaryotic cells• Cell size limited by
metabolic activities• Include plants,
animals, and fungi
LE 6-6
A typicalrod-shapedbacterium
A thin section through thebacterium Bacilluscoagulans (TEM)
0.5 µm
Pili
Nucleoid
Ribosomes
Plasmamembrane
Cell wall
Capsule
Flagella
Bacterialchromosome
LE 6-7
Total surface area(height x width xnumber of sides xnumber of boxes)
6
125 125
150 750
1
11
5
1.2 66
Total volume(height x width x lengthX number of boxes)
Surface-to-volumeratio(surface area volume)
Surface area increases whileTotal volume remains constant
LE 6-9a
Flagellum
Centrosome
CYTOSKELETON
Microfilaments
Intermediate filaments
Microtubules
Peroxisome
Microvilli
ENDOPLASMIC RETICULUM (ER
Rough ER Smooth ER
MitochondrionLysosome
Golgi apparatus
Ribosomes:
Plasma membrane
Nuclear envelope
NUCLEUS
In animal cells but not plant cells: LysosomesCentriolesFlagella (in some plant sperm)
Nucleolus
Chromatin
LE 6-9b
Roughendoplasmicreticulum
In plant cells but not animal cells: ChloroplastsCentral vacuole and tonoplastCell wallPlasmodesmata
Smoothendoplasmicreticulum
Ribosomes(small brown dots)
Central vacuole
Microfilaments
IntermediatefilamentsMicrotubules
CYTOSKELETON
Chloroplast
Plasmodesmata
Wall of adjacent cell
Cell wall
Nuclearenvelope
Nucleolus
Chromatin
NUCLEUS
Centrosome
Golgiapparatus
Mitochondrion
Peroxisome
Plasmamembrane
The Nucleus•contains most of the cell’s genes •usually the most conspicuous organelle•Enclosed by nuclear envelope
LE 6-10
Close-up of nuclearenvelope
Nucleus
Nucleolus
Chromatin
Nuclear envelope:Inner membraneOuter membrane
Nuclear pore
Porecomplex
Ribosome
Pore complexes (TEM) Nuclear lamina (TEM)
1 µm
Rough ER
Nucleus
1 µm
0.25 µm
Surface of nuclear envelope
Ribosomes•made of ribosomal RNA and protein•protein synthesis
▫In the cytosol (free ribosomes)▫On the outside of the endoplasmic reticulum
(ER) or the nuclear envelope (bound ribosomes)
LE 6-11
Ribosomes
0.5 µm
ER Cytosol
Endoplasmicreticulum (ER)
Free ribosomes
Bound ribosomes
Largesubunit
Smallsubunit
Diagram ofa ribosome
TEM showing ERand ribosomes
Endomembrane System
•Regulate protein traffic•Perform metabolic functions•Components of the endomembrane system:
▫Nuclear envelope▫Endoplasmic reticulum▫Golgi apparatus▫Lysosomes▫Vacuoles▫Plasma membrane
• components are either continuous or connected via transfer by vesicles
The Endoplasmic Reticulum (ER)
•is continuous with the nuclear envelope•two distinct regions of ER:
▫Smooth ER, lacks ribosomes
▫Rough ER with ribosomes studding its surface
LE 6-12
Ribosomes
Smooth ER
Rough ER
ER lumen
Cisternae
Transport vesicle
Smooth ER Rough ER
Transitional ER
200 nm
Nuclearenvelope
Functions of Smooth ER•Synthesizes lipids•Metabolizes carbohydrates•Stores calcium•Detoxifies poison
Functions of Rough ER•bound ribosomes•Produces proteins and membranes
▫distributed by transport vesicles
The Golgi Apparatus
•consists of flattened membranous sacs called cisternae
•Functions of the Golgi apparatus:▫Modifies products of the ER▫Manufactures certain macromolecules▫Sorts and packages materials into
transport vesicles
LE 6-13
trans face(“shipping” side ofGolgi apparatus) TEM of Golgi apparatus
0.1 µm
Golgi apparatus
cis face(“receiving” side ofGolgi apparatus)
Vesicles coalesce toform new cis Golgi cisternae Vesicles also
transport certainproteins back to ER
Vesicles movefrom ER to Golgi
Vesicles transport specificproteins backward to newerGolgi cisternae
Cisternalmaturation:Golgi cisternaemove in a cis-to-transdirection
Vesicles form andleave Golgi, carryingspecific proteins toother locations or tothe plasma mem-brane for secretion
Cisternae
Lysosomes•membranous sac of hydrolytic enzymes
▫hydrolyze proteins, fats, polysaccharides, and nucleic acids
▫use enzymes to recycle organelles and macromolecules a process called autophagy
LE 6-14a
Phagocytosis: lysosome digesting food
1 µm
Plasmamembrane
Food vacuole
Lysosome
Nucleus
Digestiveenzymes
Digestion
Lysosome
Lysosome containsactive hydrolyticenzymes
Food vacuolefuses withlysosome
Hydrolyticenzymes digestfood particles
LE 6-14b
Autophagy: lysosome breaking down damaged organelle
1 µm
Vesicle containingdamaged mitochondrion
Mitochondrionfragment
Lysosome containingtwo damaged organelles
Digestion
Lysosome
Lysosome fuses withvesicle containingdamaged organelle
Peroxisomefragment
Hydrolytic enzymesdigest organellecomponents
Vacuoles & Vesicles•membrane-bound sacs with varied functions
▫Food vacuoles formed by phagocytosis
▫Contractile vacuoles found in many freshwater protists pump excess water out of cells
▫Central vacuoles found in many mature plant cells hold organic compounds and water
LE 6-16-3
Nuclear envelope
Nucleus
Rough ER
Smooth ER
Transport vesicle
cis Golgi
trans Golgi
Plasma membrane
Mitochondria & ChloroplastsMitochondria Chloroplasts
• sites of cellular respiration• not part of the
endomembrane system
• found only in plants and algae
• the sites of photosynthesis• not part of the
endomembrane system
Mitochondria•in nearly all eukaryotic cells•smooth outer membrane•inner membrane folded into cristae
▫creates two compartments: intermembrane space mitochondrial matrix
▫Folding creates more surface area for enzymes that synthesize ATP
LE 6-17
Mitochondrion
Intermembrane space
Outer membrane
Inner membrane
Cristae
Matrix
100 nmMitochondrialDNA
Freeribosomes in themitochondrialmatrix
Chloroplasts•Type of plastid•contain the green pigment chlorophyll•contains enzymes and other molecules that
function in photosynthesis•found in leaves and other green organs of
plants and in algae•Chloroplast structure includes:
▫Thylakoids membranous sacs
▫Stroma the internal fluid
Plastids
•Responsible for photosynthesis•Storage of products (ie. Starch)•Synthesis of molecules (ie. Fatty acids)
Peroxisomes
•specialized metabolic compartments •single membrane•produce hydrogen peroxide and convert it to water•are oxidative organelles•Aid in breakdown of lipids
Cytoskeleton•network of fibers extending throughout the
cytoplasm•organizes the cell’s structures and activities•anchors many organelles•composed of:
▫Microtubules▫Microfilaments▫Intermediate filaments
Roles of the Cytoskeleton•support the cell •maintain cell shape•interacts with motor proteins to produce
motility•Inside the cell, vesicles can travel along
“monorails” provided by the cytoskeleton•may help regulate biochemical activities
Centrosomes and Centrioles•microtubules grow out from a centrosome
near the nucleus•“microtubule-organizing center”•In animal cells, the centrosome has a pair
of centrioles
LE 6-22
0.25 µm
Microtubule
Centrosome
Centrioles
Longitudinal sectionof one centriole
Microtubules Cross sectionof the other centriole
Cilia and Flagella•Beating controlled by microtubules•sheathed by the plasma membrane•Dynein
▫Motor protein▫drives the bending movements of a cilium or
flagellum
LE 6-23b
15 µm
Direction of organism’s movement
Motion of cilia
Direction ofactive stroke
Direction ofrecovery stroke
Microfilaments (Actin Filaments)•twisted double chain of actin subunits
▫Also have myosin if the microfilaments are used for movement
•bear tension, resisting pulling forces within the cell
• form a 3D network just inside the plasma membrane to help support the cell’s shape
•Bundles of microfilaments make up the core of microvilli
LE 6-27b
Cortex (outer cytoplasm):gel with actin network
Amoeboid movement
Inner cytoplasm: solwith actin subunits
Extendingpseudopodium
•Cytoplasmic streaming ▫circular flow of cytoplasm within cells▫speeds distribution of materials within the
cell▫In plant cells, actin-myosin interactions and
sol-gel transformations drive cytoplasmic streaming
LE 6-27c
Nonmovingcytoplasm (gel)
Cytoplasmic streaming in plant cells
Chloroplast
Streamingcytoplasm(sol)
Cell wall
Parallel actinfilaments
Vacuole
Intermediate Filaments•range in diameter from 8–12 nanometers
▫ larger than microfilaments▫smaller than microtubules
•support cell shape•fix organelles in place
Extracellular Structures
•These extracellular structures include:▫ Cell walls of plants▫The extracellular matrix (ECM) of animal
cells▫Intercellular junctions
Cell Walls of Plants•distinguishes plant cells from animal cells•protects the plant cell•maintains cell shape•prevents excessive uptake of water•made of cellulose fibers embedded in other
polysaccharides and protein
Cell Walls of Plants•Plant cell walls may have multiple layers:
▫Primary cell wall relatively thin and flexible
▫Middle lamella thin layer between primary walls of adjacent
cells▫Secondary cell wall (in some cells)
added between the plasma membrane and the primary cell wall
• Plasmodesmata are channels between adjacent plant cells
LE 6-28
Centralvacuole of cell
PlasmamembraneSecondarycell wall
Primarycell wall
Middlelamella
1 µm
Centralvacuole of cell
Central vacuoleCytosol
Plasma membrane
Plant cell walls
Plasmodesmata
The Extracellular Matrix (ECM) of Animal Cells•made up of glycoproteins and other
macromolecules•Functions of the ECM:
▫Support▫Adhesion▫Movement▫Regulation
Plants: Plasmodesmata•channels that perforate plant cell walls
▫water and small solutes (and sometimes proteins and RNA) can pass from cell to cell
Animals: Tight Junctions, Desmosomes, and Gap Junctions
• tight junctions▫membranes of neighboring cells are pressed
together▫prevents leakage of extracellular fluid
• Desmosomes (anchoring junctions) ▫fasten cells together into strong sheets
• Gap junctions (communicating junctions) ▫provide cytoplasmic channels between adjacent
cells
LE 6-31
Tight junctions preventfluid from moving across a layer of cells
Tight junction
0.5 µm
1 µm
0.1 µm
Gap junction
Extracellularmatrix
Spacebetweencells
Plasma membranesof adjacent cells
Intermediatefilaments
Tight junction
Desmosome
Gapjunctions
Fluidity of Membranes
•Phospholipids move within the bilayer•Most of the lipids, and some proteins, drift
laterally
•Cool temperatures▫membranes switch from a fluid state to a solid
state
•Membranes must be fluid to work properly▫Consistency of oil
•Cholesterol▫Steroid present in cell membrane▫Maintains fluidity
At warm temperatures (such as 37°C) restrains movement
At cool temperatures prevents tight packing
Membrane Proteins
•Peripheral proteins▫not embedded
•Integral proteins ▫penetrate the hydrophobic core ▫often span the membrane
transmembrane proteins
LE 7-7
Fibers ofextracellular
matrix (ECM)
Glycoprotein
Carbohydrate
Microfilamentsof cytoskeleton
Cholesterol
Integralprotein
Peripheralproteins
CYTOPLASMIC SIDEOF MEMBRANE
EXTRACELLULARSIDE OF
MEMBRANE
Glycolipid
•Six major functions of membrane proteins:▫Transport▫Enzymatic activity▫Signal transduction▫Cell-cell recognition▫Intercellular joining▫Attachment to the cytoskeleton and
extracellular matrix (ECM)
LE 7-9b
Glyco-protein
Cell-cell recognition Intercellular joining Attachment to thecytoskeleton and extra-
cellular matrix (ECM)
• Carbohydrates • Cell to cell recognition
• Bonded to lipids = glycolipids• Bonded to proteins = glycoproteins (more
common)
Selective Permeability
•Permeability factors▫Molecular size
▫Solubility in lipids ex. Oxygen, carbon dioxide, steroid hormones
▫Charge of ions
▫Presence of carrier molecules
Carrier Molecules
•transport proteins▫channel proteins• carrier proteins• bind to molecules• change shape to shuttle them across the
membrane
•Diffusion▫Net direction of movement from areas of
high to low concentration▫Continues until equilibrium has been met
Movement continues at equal rates in both directions
Animation: Membrane Selectivity Animation: Diffusion
LE 7-11a
Molecules of dye Membrane (cross section)
WATER
Net diffusion Net diffusion Equilibrium
Diffusion of one solute
•Osmosis ▫diffusion of water▫direction of osmosis is determined by a
difference in total solute concentration Movement from region of lower solute
concentration to the region of higher solute concentration
•Tonicity ▫the ability of a solution to cause a cell to gain or lose water
• Isotonic solution:▫ solute concentration is the same as that inside the cell▫no net water movement across the plasma membrane
•Hypertonic solution▫solute concentration is greater than that inside the cell▫cell loses water
•Hypotonic solution▫solute concentration is less than that inside the cell▫cell gains water
Cells without Cell Walls•Special adaptations for osmoregulation
▫Control of water balance Ex. Contractile vacuole in Paramecium
Cells with Cell Walls•Cell walls help maintain water balance
▫hypotonic solution swells until the wall opposes uptake the cell is now turgid (firm)
▫Isotonic is no net movement of water into the cell the cell becomes flaccid (limp), and the plant may wilt
▫hypertonic environment plant cells lose water the membrane pulls away from the wall
a usually lethal effect called plasmolysis
LE 7-13
Animalcell
Lysed
H2O H2O H2O
Normal
Hypotonic solution Isotonic solution Hypertonic solution
H2O
Shriveled
H2OH2OH2OH2OPlantcell
Turgid (normal) Flaccid Plasmolyzed
•Facilitated diffusion▫passive
solute moves down its concentration gradient▫Transport proteins
Channel proteins Carrier proteins
•Active transport ▫moves substances against their
concentration gradient▫requires energy, usually in the form of ATP▫Integral proteins
Ex. sodium-potassium pump
Animation: Active Transport
•Membrane potential ▫voltage difference across a membrane
•Electrochemical gradient▫drives the diffusion of ions across a membrane▫Includes :
A chemical force the ion’s concentration gradient
An electrical force the effect of the membrane potential on the ion’s
movement
• electrogenic pump• transport protein• generates the voltage across a membrane
main electrogenic pump of plants, fungi, and bacteria is a proton pump
•Cotransport ▫active transport of a solute indirectly drives
transport of another solute Ex. Plants - gradient of hydrogen ions
generated by proton pumps drives active transport of nutrients into the cell
LE 7-19
H+
ATP
Proton pump
Sucrose-H+
cotransporter
Diffusionof H+
Sucrose
H+
H+
H+
H+
H+
H+
+
+
+
+
+
+
–
–
–
–
–
–
•Exocytosis▫Type of active transport▫transport vesicles migrate to the
membrane, fuse with it, and release their contents
•Endocytosis▫cell takes in macromolecules by forming vesicles from the
plasma membrane▫reversal of exocytosis▫involves different proteins
• Three types of endocytosis:▫Phagocytosis
“cellular eating” Cell engulfs particle in a vacuole
▫Pinocytosis “cellular drinking” Cell creates vesicle around fluid
▫Receptor-mediated endocytosis Binding of ligands to receptors triggers vesicle formation
Figure 3-11
2 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Cell membraneof phagocytic
cell
Figure 3-11
3 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
Figure 3-11
4 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Vesicle
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
The vesicle moves into the cytoplasm.
Figure 3-11
5 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Vesicle
Lysosomes
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
The vesicle moves into the cytoplasm.
Lysosomes fuse with the vesicle.
Figure 3-11
6 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Vesicle
Lysosomes
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
The vesicle moves into the cytoplasm.
Lysosomes fuse with the vesicle.
This fusion activates digestive enzymes.
Figure 3-11
7 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Vesicle
Lysosomes
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
The vesicle moves into the cytoplasm.
Lysosomes fuse with the vesicle.
This fusion activates digestive enzymes.
The enzymes break down the structure of the phagocytized
material.
Figure 3-11
8 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
Cell membraneof phagocytic
cell
Phagocytosis
A phagocytic cell comes in contact with the foreign object and sends
pseudopodia (cytoplasmic extensions) around it.
Pseudopodium(cytoplasmic
extension)
EXTRACELLULAR FLUID
CYTOPLASM
Foreignobject
Vesicle
Lysosomes
Undissolvedresidue
The pseudopodia approach one another and fuse to trap the
material within the vesicle.
The vesicle moves into the cytoplasm.
Lysosomes fuse with the vesicle.
This fusion activates digestive enzymes.
The enzymes break down the structure of the phagocytized
material.
Residue is then ejected from the cell by exocytosis.
LE 7-20c
Receptor
RECEPTOR-MEDIATED ENDOCYTOSIS
Ligand
Coatedpit
Coatedvesicle
Coat protein
Coat protein
Plasmamembrane
0.25 µm
A coated pitand a coated
vesicle formedduring
receptor-mediated
endocytosis(TEMs).
Figure 3-10
2 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Ligands Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Figure 3-10
3 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Ligands
Endocytosis
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Figure 3-10
4 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Coatedvesicle
Ligands
Endocytosis
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Pockets pinch off, forming vesicles.
Figure 3-10
5 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Coatedvesicle
Ligands
Endocytosis
Lysosome
Fused vesicleand lysosome
Fusion
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Pockets pinch off, forming vesicles.
Vesicles fuse with lysosomes.
Figure 3-10
6 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Coatedvesicle
Ligands
Endocytosis
Lysosome
Fused vesicleand lysosome
Fusion
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Pockets pinch off, forming vesicles.
Vesicles fuse with lysosomes.
Ligands are removed and absorbed into the cytoplasm.
Figure 3-10
7 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Ligandreceptors
CYTOPLASM
Coatedvesicle
Ligands
Endocytosis
Lysosome
Fused vesicleand lysosome
Ligandsremoved
FusionDetachment
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Pockets pinch off, forming vesicles.
Vesicles fuse with lysosomes.
Ligands are removed and absorbed into the cytoplasm.
The membrane containing the receptor molecules separates from
the lysosome.
Figure 3-10
8 of 8Copyright © 2007 Pearson Education, Inc., publishing as Benjamin Cummings
EXTRACELLULARFLUID Ligands binding
to receptors
Exocytosis
Ligandreceptors
CYTOPLASM
Coatedvesicle
Ligands
Endocytosis
Lysosome
Fused vesicleand lysosome
Ligandsremoved
FusionDetachment
Receptor-Mediated Endocytosis
Target molecules (ligands) bind to receptors in cell membrane.
Areas coated with ligands form deep pockets in membrane surface.
Pockets pinch off, forming vesicles.
Vesicles fuse with lysosomes.
Ligands are removed and absorbed into the cytoplasm.
The membrane containing the receptor molecules separates from
the lysosome.
The vesicle returns to the surface.
Cell to Cell Communication•signal-transduction pathway
▫A signal on a cell’s surface is converted into a specific cellular response
•chemical messengers▫cell junctions
directly connect the cytoplasm of adjacent cells
• local signaling▫communicate by direct contact
Some animal cells
LE 11-3Plasma membranes
Gap junctionsbetween animal cells
Cell junctions
Cell-cell recognition
Plasmodesmatabetween plant cells
•local regulators▫messenger molecules that travel only short
distances Some animal cells
•long-distance signaling▫Hormones
plants and animals
LE 11-4
Paracrine signaling
Local regulatordiffuses throughextracellular fluid
Secretoryvesicle
Secretingcell
Target cell
Local signaling
Electrical signalalong nerve celltriggers release ofneurotransmitter
Neurotransmitter diffuses across synapse
Endocrine cell Bloodvessel
Long-distance signaling
Hormone travelsin bloodstreamto target cells
Synaptic signaling
Target cellis stimulated
Hormonal signaling
Target cell
Cell Signaling
•Cells receiving signals went through three processes:▫Reception▫Transduction▫Response
LE 11-5_1
EXTRACELLULARFLUID
Reception
Plasma membrane
Transduction
CYTOPLASM
Receptor
Signalmolecule
LE 11-5_2
EXTRACELLULARFLUID
Reception
Plasma membrane
Transduction
CYTOPLASM
Receptor
Signalmolecule
Relay molecules in a signal transductionpathway
LE 11-5_3
EXTRACELLULARFLUID
Reception
Plasma membrane
Transduction
CYTOPLASM
Receptor
Signalmolecule
Relay molecules in a signal transductionpathway
Response
Activationof cellularresponse
•Reception ▫binding between a signal molecule (ligand)
and receptor highly specific
▫conformational change in a receptor Often the initial transduction of the signal
▫Most signal receptors are plasma membrane proteins
LE 11-7c
Signalmolecule(ligand)
Gateclosed Ions
Ligand-gatedion channel receptor
Plasmamembrane
Gate closed
Gate open
Cellularresponse
•Transduction▫Multistep pathways ▫can amplify a signal▫opportunities for coordination and
regulation
•Multistep pathways have two important benefits:▫Amplifying the signal (and thus the
response)▫Contributing to the specificity of the
response
LE 11-8Signal molecule
Activated relaymolecule
Receptor
Inactiveprotein kinase
1 Activeprotein kinase
1
Inactiveprotein kinase
2 Activeprotein kinase
2
Inactiveprotein kinase
3 Activeprotein kinase
3
ADP
Inactiveprotein
Activeprotein
Cellularresponse
Phosphorylation cascade
ATP
PPP i
ADPATP
PPP i
ADPATP
PPP i
P
P
P
• Cyclic AMP (cAMP) • one of the most widely used second
messengers• Adenylyl cyclase• enzyme in the plasma membrane• converts ATP to cAMP in response to an
extracellular signal