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Copyright © 2010 Pearson Education, Inc.
Cells- Part B
• Cell Organelle and DNA
Copyright © 2010 Pearson Education, Inc.
Cytoplasm
• Located between plasma membrane and nucleus
• Cytosol
• Water with solutes (protein, salts, sugars, etc.)
• Cytoplasmic organelles
• Metabolic machinery of cell
• Inclusions
• Granules of glycogen or pigments, lipid droplets, vacuoles, and crystals
Copyright © 2010 Pearson Education, Inc.
Cytoplasmic Organelles
• Membranous
• Mitochondria
• Peroxisomes
• Lysosomes
• Endoplasmic reticulum
• Golgi apparatus
• Nonmembranous
• Cytoskeleton
• Centrioles
• Ribosomes
Copyright © 2010 Pearson Education, Inc.
Mitochondria
• Double-membrane structure with shelflike cristae
• Provide most of cell’s ATP via aerobic cellular respiration
• Contain their own DNA and RNA
Copyright © 2010 Pearson Education, Inc. Figure 3.17
Enzymes
Matrix
Cristae
Mitochondrial DNA
Ribosome
Outer mitochondrial membrane
Inner mitochondrial membrane
(b)
(a)
(c)
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Ribosomes
• Granules containing protein and rRNA
• Site of protein synthesis
• Free ribosomes synthesize soluble proteins
• Membrane-bound ribosomes (on rough ER) synthesize proteins to be incorporated into membranes or exported from the cell
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Endoplasmic Reticulum (ER)
• Interconnected tubes and parallel membranes enclosing cisternae
• Continuous with nuclear membrane
• Two varieties:
• Rough ER
• Smooth ER
Copyright © 2010 Pearson Education, Inc. Figure 3.18a
Nuclearenvelope
Ribosomes
Rough ER
Smooth ER
(a) Diagrammatic view of smooth and rough ER
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Rough ER
• External surface studded with ribosomes
• Manufactures all secreted proteins
• Synthesizes membrane integral proteins and phospholipids
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Smooth ER
• Tubules arranged in a looping network
• Enzyme (integral protein) functions:
• In the liver—lipid and cholesterol metabolism, breakdown of glycogen, and, along with kidneys, detoxification of drugs, pesticides, and carcinogens
• Synthesis of steroid-based hormones
• In intestinal cells—absorption, synthesis, and transport of fats
• In skeletal and cardiac muscle—storage and release of calcium
Copyright © 2010 Pearson Education, Inc.
Golgi Apparatus
• Stacked and flattened membranous sacs
• Modifies, concentrates, and packages proteins and lipids
• Transport vessels from ER fuse with convex cis face of Golgi apparatus
• Proteins then pass through Golgi apparatus to trans face
• Secretory vesicles leave trans face of Golgi stack and move to designated parts of cell
Copyright © 2010 Pearson Education, Inc. Figure 3.20
Protein-containing vesicles pinch off rough ERand migrate to fuse with membranes ofGolgi apparatus.
Proteins aremodified withinthe Golgi compartments.
Proteins arethen packagedwithin differentvesicle types, depending ontheir ultimatedestination.
Plasmamem-brane
Secretion byexocytosis
Vesicle becomeslysosome
Golgiapparatus
Rough ER ERmembrane
Phagosome
Proteins incisterna
Pathway B:Vesicle membraneto be incorporatedinto plasmamembranePathway A:
Vesicle contentsdestined for exocytosis Extracellular fluid
Secretoryvesicle
Pathway C:Lysosome containing acid hydrolaseenzymes
1
3
2
Copyright © 2010 Pearson Education, Inc.
Lysosomes
• Spherical membranous bags containing digestive enzymes (acid hydrolases)
• Digest ingested bacteria, viruses, and toxins
• Degrade nonfunctional organelles
• Break down and release glycogen
• Break down bone to release Ca2+
• Destroy cells in injured or nonuseful tissue (autolysis)
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Endomembrane System
• Overall function
• Produce, store, and export biological molecules
• Degrade potentially harmful substances
Copyright © 2010 Pearson Education, Inc. Figure 3.22
Golgiapparatus
Transportvesicle
Plasmamembrane
Vesicle
Smooth ER
Rough ER
Nuclear envelope
Lysosome
Nucleus
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Endomembrane System
PLAYPLAY Animation: Endomembrane System
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Peroxisomes
• Membranous sacs containing powerful oxidases and catalases
• Detoxify harmful or toxic substances
• Neutralize dangerous free radicals (highly reactive chemicals with unpaired electrons)
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Cytoskeleton
• Elaborate series of rods throughout cytosol
• Microtubules
• Microfilaments
• Intermediate filaments
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Microfilaments
• Dynamic actin strands attached to cytoplasmic side of plasma membrane
• Involved in cell motility, change in shape, endocytosis and exocytosis
Copyright © 2010 Pearson Education, Inc. Figure 3.23a
Strands made of sphericalprotein subunits called actins
(a) Microfilaments
Actin subunit
7 nm
Microfilaments form the blue networksurrounding the pink nucleus in thisphoto.
Copyright © 2010 Pearson Education, Inc.
Intermediate Filaments
• Tough, insoluble ropelike protein fibers
• Resist pulling forces on the cell and attach to desmosomes
Copyright © 2010 Pearson Education, Inc. Figure 3.23b
(b) Intermediate filaments
Tough, insoluble protein fibersconstructed like woven ropes
10 nm
Fibrous subunits
Intermediate filaments form the purplebatlike network in this photo.
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Microtubules
• Dynamic hollow tubes
• Most radiate from centrosome
• Determine overall shape of cell and distribution of organelles
Copyright © 2010 Pearson Education, Inc. Figure 3.23c
(c) MicrotubulesHollow tubes of spherical protein
subunits called tubulins
25 nm
Tubulin subunits
Microtubules appear as gold networkssurrounding the cells’ pink nuclei inthis photo.
Copyright © 2010 Pearson Education, Inc.
Motor Molecules
• Protein complexes that function in motility (e.g., movement of organelles and contraction)
• Powered by ATP
Copyright © 2010 Pearson Education, Inc. Figure 3.24
Cytoskeletal elements(microtubules or microfilaments)
Motor molecule (ATP powered)
ATP
(b) In some types of cell motility, motor molecules attached to oneelement of the cytoskeleton can cause it to slide over anotherelement, as in muscle contraction and cilia movement.
ATP
Vesicle
(a) Motor molecules can attach to receptors onvesicles or organelles, and “walk” the organellesalong the microtubules of the cytoskeleton.
Motor molecule (ATP powered)
Microtubule of cytoskeleton
Receptor for motor molecule
Copyright © 2010 Pearson Education, Inc.
Centrosome
• “Cell center” near nucleus
• Generates microtubules; organizes mitotic spindle
• Contains centrioles: Small tube formed by microtubules
Copyright © 2010 Pearson Education, Inc. Figure 3.25a
Centrosome matrix
(a)
Centrioles
Microtubules
Copyright © 2010 Pearson Education, Inc.
Cellular Extensions
• Cilia and flagella
• Whiplike, motile extensions on surfaces of certain cells
• Contain microtubules and motor molecules
• Cilia move substances across cell surfaces
• Longer flagella propel whole cells (tail of sperm)
PLAYPLAY Animation: Cilia and Flagella
Copyright © 2010 Pearson Education, Inc. Figure 3.26
Plasmamembrane
Outer microtubuledoublet
Dynein arms
Centralmicrotubule
Radial spoke
Radial spoke
TEM
TEM
Triplet
Basal body(centriole)
Cilium
Microtubules
Plasmamembrane
Basal body
Cross-linkingproteins insideouter doublets
Cross-linkingproteins insideouter doublets
A longitudinal section of acilium shows microtubules running the length of thestructure.
The doubletsalso have attached motor proteins, the dynein arms.
The outermicrotubule doublets and the two central microtubules are held together by cross-linking proteins and radial spokes.
A cross section through thebasal body. The nine outer doublets of a cilium extend into a basal body where each doublet joins another microtubule to form a ring of nine triplets.
A cross section through thecilium shows the “9 + 2”arrangement of microtubules.
TEM
Copyright © 2010 Pearson Education, Inc. Figure 3.27
(a) Phases of ciliary motion.
(b) Traveling wave created by the activity ofmany cilia acting together propels mucusacross cell surfaces.
Power, orpropulsive,stroke
Layer of mucus
Cell surface
Recovery stroke, whencilium is returning to itsinitial position
1 2 3 4 5 6 7
Copyright © 2010 Pearson Education, Inc.
Cellular Extensions
• Microvilli
• Fingerlike extensions of plasma membrane
• Increase surface area for absorption
• Core of actin filaments for stiffening
Copyright © 2010 Pearson Education, Inc. Figure 3.28
Microvillus
Actinfilaments
Terminalweb
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Nucleus
• Genetic library with blueprints for nearly all cellular proteins
• Responds to signals and dictates kinds and amounts of proteins to be synthesized
• Most cells are uninucleate
• Red blood cells are anucleate
• Skeletal muscle cells, bone destruction cells, and some liver cells are multinucleate
Copyright © 2010 Pearson Education, Inc. Figure 3.29a
Chromatin (condensed)
Nuclear envelope Nucleus
Nuclear pores
Nucleolus
Cisternae of rough ER
(a)
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Nuclear Envelope
• Double-membrane barrier containing pores
• Outer layer is continuous with rough ER and bears ribosomes
• Inner lining (nuclear lamina) maintains shape of nucleus
• Pore complex regulates transport of large molecules into and out of nucleus
Copyright © 2010 Pearson Education, Inc. Figure 3.29b
Nucleus
Nuclearpores
Fractureline of outermembrane
Nuclear pore complexes.Each pore is ringed byprotein particles.
Surface of nuclear envelope.
Nuclear lamina. The netlikelamina composed of inter-mediate filaments formed bylamins lines the inner surfaceof the nuclear envelope.
(b)
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Nucleoli
• Dark-staining spherical bodies within nucleus
• Involved in rRNA synthesis and ribosome subunit assembly
Copyright © 2010 Pearson Education, Inc.
Chromatin
• Threadlike strands of DNA (30%), histone proteins (60%), and RNA (10%)
• Arranged in fundamental units called nucleosomes
• Condense into barlike bodies called chromosomes when the cell starts to divide
Copyright © 2010 Pearson Education, Inc. Figure 3.30
Metaphasechromosome(at midpointof cell division)
Nucleosome (10-nm diameter; eight histone proteins wrapped by two winds of the DNA double helix)
Linker DNA
Histones
(a)
(b)
1 DNA doublehelix (2-nm diameter)
2 Chromatin(“beads on a string”) structurewith nucleosomes
3 Tight helical fiber(30-nm diameter)
5 Chromatid(700-nm diameter)
4 Looped domain structure (300-nm diameter)