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Chapter 6 A Tour of the Cell PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece Lectures by Chris Romero Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 10 µm Overview: The Importance of Cells • All organisms are made of cells • The cell is the simplest collection of matter that can live How old is the earth? How do we know? What was it like back then (young planet)? How did life 1st come about? The probable evolution of cells was posited by A. Oparin (1920’s): “chemical evolution” Inorganic compounds (CHONPS) organic molecules primitive cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The chemical evolution of cells • Had to start with building blocks • The Miller-Urey experiment • The experiment used water (H2O), methane (CH4), ammonia (NH3), and hydrogen (H2). • The chemicals were all sealed inside a sterile array of glass tubes and flasks connected in a loop, with one flask halffull of liquid water and another flask containing a pair of electrodes. • The liquid water was heated to induce evaporation, sparks were fired between the electrodes to simulate lightning through the atmosphere and water vapor, and then the atmosphere was cooled again so that the water could condense and trickle back into the first flask in a continuous cycle. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The result: • At the end of one week of continuous operation, Miller and Urey observed that as much as 10–15% of the carbon within the system was now in the form of organic compounds. • Two percent of the carbon had formed amino acids that are used to make proteins in living cells, with glycine as the most abundant. • Sugars, lipids, and some of the building blocks for nucleic acids were also formed. (Wikipedia) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings From organic molecules to cells… • It’s proposed that this “primordial soup” of organics in the young oceans may have puddled together, condensed/evaporated into self-sustaining “globs” = primitive cells? Some labs have since been able to replicate this process (make primitive “beginner-level” protocells) • Microspheres • Coacervates Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Once upon a time, about 3.5 billion years ago… Self-replicating molecules First to appear were self-replicating molecules. Then these molecules became more complicated and evolved a membrane inside which they were protected from the changing external environment. These were the first cells that became primitive bacteria, termed Prokaryotes. • Archaebacteria • “Extremophiles” Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Then what happened? • According to some more recent findings, many scientists have pushed back the origin of cells to around 3.8 billion years! • The first cells were likely heterotrophic and anaerobic • According to the heterotroph hypothesis, autotrophs developed after the evolution of heterotrophs partly because the primitive atmosphere of the earth lacked oxygen. • Oxygen built up as a result of photosynthesis. There is no evidence of plants or cyanobacteria in the fossil record before about 2 billion years ago. Also rocks containing oxides (elements combined with oxygen) don't appear until then either. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings What about eukaryotic cells? • Evolved around 1.75 – 2 billion years ago • “The Endosymbiont Hypothesis” (Lynn Margulis) • narrated animation Supporting evidence: • Both mitochondria and plastids contain DNA that is different from that of the cell nucleus and that is similar to that of bacteria (in being circular and in its size). • They are surrounded by two or more membranes, and the innermost of these shows differences in composition from the other membranes of the cell. The composition is like that of a prokaryotic cell membrane. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Multicellularity • 1st multicellular eukaryotes seem to have evolved about a billion years ago • Algae, kelp, fungi • May have come about as colonial groups of individual cells that have division of labor Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cell anatomy reflects function • Concept 6.1: To study cells, biologists use microscopes and the tools of biochemistry 1m 0.1 m Human height Length of some nerve and muscle cells Chicken egg 1 cm Light microscope • Scientists use microscopes to visualize cells too small to see with the naked eye 10 m Measurements 1 centimeter (cm) = 102 meter (m) = 0.4 inch 1 millimeter (mm) = 10–3 m 1 micrometer (µm) = 10–3 mm = 10–6 m 1 nanometer (nm) = 10–3 mm = 10–9 m – Can be used to visualize different sized cellular structures Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 10 µ m 1µm 100 nm Most plant and Animal cells Nucleus Most bacteria Mitochondrion Smallest bacteria Viruses 10 nm Ribosomes Proteins 1 nm Lipids Small molecules Figure 6.2 0.1 nm Atoms Electron microscope • Different types of microscopes 100 µm Electron microscope Frog egg 1 mm • Light microscopes (LMs) – Pass visible light through a specimen – Magnify cellular structures with lenses Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Electron microscopes (EMs) – Focus a beam of electrons through a specimen (TEM) or onto its surface (SEM) • The scanning electron microscope (SEM) – Provides for detailed study of the surface of a specimen TECHNIQUE RESULTS 1 µm Cilia (a) Scanning electron microscopy (SEM). Micrographs taken with a scanning electron microscope show a 3D image of the surface of a specimen. This SEM shows the surface of a cell from a rabbit trachea (windpipe) covered with motile organelles called cilia. Beating of the cilia helps move inhaled debris upward toward the throat. Figure 6.4 (a) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The transmission electron microscope (TEM) – Provides for detailed study of the internal ultrastructure of cells Longitudinal section of cilium (b) Transmission electron microscopy (TEM). A transmission electron microscope profiles a thin section of a specimen. Here we see a section through a tracheal cell, revealing its ultrastructure. In preparing the TEM, some cilia were cut along their lengths, creating longitudinal sections, while other cilia were cut straight across, creating cross sections. Figure 6.4 (b) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cross section of cilium 1 µm Isolating Organelles by Cell Fractionation • Cell fractionation – Takes cells apart and separates the major organelles from one another Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The centrifuge – Is used to fractionate cells into their component parts Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Comparing Prokaryotic and Eukaryotic Cells • All cells have several basic features in common • They are bounded by a plasma membrane • They contain a semifluid substance called the cytosol • They contain chromosomes • They all have ribosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Two types of cells make up every organism Prokaryotic cells Eukaryotic cells • Do not contain a nucleus • Have a membranebound nucleus • Have their DNA located in a region called the nucleoid • Have membrane-bound organelles that compartmentalize their functions Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Pili: attachment structures on the surface of some prokaryotes Nucleoid: region where the cell’s DNA is located (not enclosed by a membrane) Ribosomes: organelles that synthesize proteins Bacterial chromosome (a) A typical rod-shaped bacterium Plasma membrane: membrane enclosing the cytoplasm Cell wall: rigid structure outside the plasma membrane Capsule: jelly-like outer coating of many prokaryotes 0.5 µm Flagella: locomotion organelles of some bacteria Figure 6.6 A, B Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings (b) A thin section through the bacterium Bacillus coagulans (TEM) • Eukaryotic cells – Contain a true nucleus, bounded by a membranous nuclear envelope – Are generally quite a bit bigger than prokaryotic cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Limitations of Cell Size: Surface Area to Volume Ratio • The logistics of carrying out cellular metabolism sets limits on the size of cells Surface area increases while total volume remains constant • A smaller cell has a higher surface to volume ratio, which facilitates the exchange of materials into and out of the cell 5 1 1 Total surface area (height width number of sides number of boxes) 6 150 750 Total volume (height width length number of boxes) 1 125 125 Surface-to-volume ratio (surface area volume) 6 12 6 Figure 6.7 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cell Membrane • The plasma membrane – Functions as a selective barrier – Allows sufficient passage of nutrients and waste Outside of cell Carbohydrate side chain Hydrophilic region Inside of cell 0.1 µm Hydrophobic region Figure 6.8 A, B (a) TEM of a plasma membrane. The plasma membrane, here in a red blood cell, appears as a pair of dark bands separated by a light band. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Hydrophilic region Phospholipid Proteins (b) Structure of the plasma membrane A Panoramic View of the Eukaryotic Cell • Eukaryotic cells – Have extensive and elaborately arranged internal membranes, which form organelles • Plant and animal cells have most of the same organelles • Tutorial on parts of a typical animal cell Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • A animal cell ENDOPLASMIC RETICULUM (ER) Rough ER Smooth ER Nuclear envelope Nucleolus NUCLEUS Chromatin Flagelium Plasma membrane Centrosome CYTOSKELETON Microfilaments Intermediate filaments Ribosomes Microtubules Microvilli Golgi apparatus Peroxisome Figure 6.9 Mitochondrion Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Lysosome In animal cells but not plant cells: Lysosomes Centrioles Flagella (in some plant sperm) • A plant cell Nuclear envelope Nucleolus Chromatin NUCLEUS Centrosome Rough endoplasmic reticulum Smooth endoplasmic reticulum Ribosomes (small brwon dots) Central vacuole Tonoplast Golgi apparatus Microfilaments Intermediate filaments CYTOSKELETON Microtubules Mitochondrion Peroxisome Plasma membrane Chloroplast Cell wall Plasmodesmata Wall of adjacent cell Figure 6.9 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings In plant cells but not animal cells: Chloroplasts Central vacuole and tonoplast Cell wall Plasmodesmata The Nucleus: Genetic Library of the Cell • The nucleus – Contains most of the genes in the eukaryotic cell (where are the rest?) The eukaryotic cell’s genetic instructions are housed in the nucleus and carried out by the ribosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nuclear membrane • The nuclear envelope – Encloses the nucleus, separating its contents from the cytoplasm Nucleus 1 µm Nucleolus Chromatin Nucleus Nuclear envelope: Inner membrane Outer membrane Nuclear pore Pore complex Rough ER Surface of nuclear envelope. 1 µm Ribosome 0.25 µm Close-up of nuclear envelope Figure 6.10 Pore complexes (TEM). Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nuclear lamina (TEM). Ribosomes: Protein Factories in the Cell • Ribosomes – Are particles made of ribosomal RNA and protein – Carry out protein synthesis Endoplasmic reticulum (ER) Ribosomes Cytosol Free ribosomes Bound ribosomes Large subunit 0.5 µm Figure 6.11 TEM showing ER and ribosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Small subunit Diagram of a ribosome Concept 6.4: The endomembrane system regulates protein traffic and performs metabolic functions in the cell • The endomembrane system – Includes many different structures Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The Endoplasmic Reticulum: Biosynthetic Factory • The endoplasmic reticulum (ER) – Accounts for more than half the total membrane in many eukaryotic cells Smooth ER • The ER membrane is continuous with the nuclear envelope Rough ER ER lumen Cisternae Ribosomes Transitional ER Transport vesicle Smooth ER Rough ER 200 µm Figure 6.12 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nuclear envelope • There are two distinct regions of ER – Smooth ER, which lacks ribosomes – Rough ER, which contains ribosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Functions of Smooth ER • The smooth ER – Synthesizes lipids – Metabolizes carbohydrates – Stores calcium – Detoxifies poison Ex: liver cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Functions of Rough ER • The rough ER – Has bound ribosomes – Produces proteins and membranes, which are distributed by transport vesicles Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The Golgi Apparatus: Shipping and Receiving Center • The Golgi apparatus – Receives many of the transport vesicles produced in the rough ER – Consists of flattened membranous sacs called cisternae • Functions of the Golgi apparatus include – Modification of the products of the rough ER – Manufacture of certain macromolecules Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Functions of the Golgi apparatus Golgi apparatus cis face (“receiving” side of Golgi apparatus) 1 Vesicles move 2 Vesicles coalesce to 6 Vesicles also form new cis Golgi cisternae from ER to Golgi transport certain Cisternae proteins back to ER 3 Cisternal maturation: Golgi cisternae move in a cisto-trans direction Figure 6.13 5 Vesicles transport specific proteins backward to newer Golgi cisternae 4 Vesicles form and leave Golgi, carrying specific proteins to other locations or to the plasma membrane for secretion trans face (“shipping” side of Golgi apparatus) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 0.1 0 µm TEM of Golgi apparatus Lysosomes: Digestive Compartments • A lysosome – Is a membranous sac of hydrolytic enzymes – Can digest all kinds of macromolecules • Lysosomes carry out intracellular digestion by phagocytosis Nucleus Lysosome Lysosome contains active hydrolytic enzymes Food vacuole fuses with lysosome Hydrolytic enzymes digest food particles Digestive enzymes Lysosome Plasma membrane Digestion Food vacuole (a) Phagocytosis: lysosome digesting food Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 1 µm Lysosomes • Autophagy Lysosome containing two damaged organelles Animation of how lysosomes work http://highered.mcgrawhill.com/sites/0072495855/student_vi ew0/chapter2/animation__lysosomes .html 1µm Mitochondrion fragment Peroxisome fragment Lysosome fuses with vesicle containing damaged organelle Hydrolytic enzymes digest organelle components Lysosome Vesicle containing damaged mitochondrion Figure 6.14 B Digestion (b) Autophagy: lysosome breaking down damaged organelle Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Vacuoles: Diverse Maintenance Compartments • A plant or fungal cell – May have one or several vacuoles – Water, food, or waste storage • In animal cells, these are called “vesicles” Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Food vacuoles – Are formed by phagocytosis – animation • Contractile vacuoles – Pump excess water out of protist cells link Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Central vacuoles – Are found in plant cells – Hold reserves of important organic compounds and water Central vacuole Cytosol Tonoplast Nucleus Central vacuole Cell wall Chloroplast Figure 6.15 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 5 µm • Relationships among organelles of the endomembrane system 1 Nuclear envelope is connected to rough ER, which is also continuous with smooth ER Nucleus Rough ER 2 Membranes and proteins produced by the ER flow in the form of transport vesicles to the Golgi Smooth ER cis Golgi Nuclear envelop 3 Golgi pinches off transport Vesicles and other vesicles that give rise to lysosomes and Vacuoles Plasma membrane trans Golgi 4 Lysosome available for fusion with another vesicle for digestion Figure 6.16 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 5 Transport vesicle carries 6 proteins to plasma membrane for secretion Plasma membrane expands by fusion of vesicles; proteins are secreted from cell • Concept 6.5: Mitochondria and chloroplasts change energy from one form to another • Mitochondria – Are the sites of cellular respiration • Chloroplasts – Found only in plants, are the sites of photosynthesis Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Mitochondria: Chemical Energy Conversion • Mitochondria are enclosed by two membranes – Are found in nearly all eukaryotic cells – A smooth outer membrane – An inner membrane folded into cristae Mitochondrion Intermembrane space Outer membrane Free ribosomes in the mitochondrial matrix Inner membrane Cristae Matrix Figure 6.17 Mitochondrial DNA Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 100 µm Chloroplasts: Capture of Light Energy • The chloroplast – Is a specialized member of a family of closely related plant organelles called plastids – Choroplasts specifically contain chlorophyll Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Chloroplasts Are found in leaves and other green organs of plants and in algae • Chloroplast structure includes – Thylakoids, membranous sacs – Stroma, the internal fluid Chloroplast Ribosomes Stroma Chloroplast DNA Inner and outer membranes Granum 1 µm Figure 6.18 Thylakoid Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Peroxisomes: Oxidation • Peroxisomes – Produce hydrogen peroxide and convert it to water Chloroplast Peroxisome Mitochondrion Figure 6.19 1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cytoskeleton Concept 6.6: The cytoskeleton is a network of fibers that organizes structures and activities in the cell Microtubule Figure 6.20 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 0.25 µm Microfilaments Roles of the Cytoskeleton: Support, Motility, and Regulation • The cytoskeleton – Is a network of fibers extending throughout the cytoplasm • Gives mechanical support to the cell • Is involved in cell motility, which utilizes motor proteins Animated, narrated tutorial http://www.wiley.com/college/pratt/0471393878/student/anim ations/actin_myosin/index.html Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Components of the Cytoskeleton • There are three main types of fibers that make up the cytoskeleton Table 6.1 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Microtubules • Microtubules – Shape the cell – Guide movement of organelles – Help separate the chromosome copies in dividing cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Centrosomes and Centrioles • The centrosome – Is considered to be a “microtubule-organizing Centrosome center” • • Contains a pair of centrioles Microtubule These form the spindle for chromosome division in mitosis/meiosis Centrioles 0.25 µm Figure 6.22 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Longitudinal section of one centriole Microtubules Cross section of the other centriole Cilia and Flagella • Cilia and flagella – Contain specialized arrangements of microtubules – Are locomotor appendages of some cells – Animated tutorial http://programs.northlandcollege.edu/biology/Biology1111/animations/flagellum.html Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Flagella beating pattern (a) Motion of flagella. A flagellum usually undulates, its snakelike motion driving a cell in the same direction as the axis of the flagellum. Propulsion of a human sperm cell is an example of flagellatelocomotion (LM). Direction of swimming Figure 6.23 A 1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Ciliary motion (b) Motion of cilia. Cilia have a backand-forth motion that moves the cell in a direction perpendicular to the axis of the cilium. A dense nap of cilia, beating at a rate of about 40 to 60 strokes a second, covers this Colpidium, a freshwater protozoan (SEM). Figure 6.23 B 15 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Cilia and flagella share a common ultrastructure Outer microtubule doublet Dynein arms 0.1 µm Central microtubule Outer doublets cross-linking proteins inside Microtubules Radial spoke Plasma membrane Basal body (b) 0.5 µm (a) 0.1 µm Triplet (c) Figure 6.24 A-C Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cross section of basal body Plasma membrane • The protein dynein – Is responsible for the bending movement of cilia and flagella Microtubule doublets ATP Dynein arm (a) Powered by ATP, the dynein arms of one microtubule doublet grip the adjacent doublet, push it up, release, and then grip again. If the two microtubule doublets were not attached, they would slide relative to each other. Figure 6.25 A Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings ATP Outer doublets cross-linking proteins Anchorage in cell (b) In a cilium or flagellum, two adjacent doublets cannot slide far because they are physically restrained by proteins, so they bend. (Only two of the nine outer doublets in Figure 6.24b are shown here.) Figure 6.25 B Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 1 3 2 (c) Localized, synchronized activation of many dynein arms probably causes a bend to begin at the base of the Cilium or flagellum and move outward toward the tip. Many successive bends, such as the ones shown here to the left and right, result in a wavelike motion. In this diagram, the two central microtubules and the cross-linking proteins are not shown. Figure 6.25 C Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Microfilaments (Actin Filaments) • Microfilaments are built from molecules of the protein actin • Are found in microvilli Microvillus Plasma membrane Microfilaments (actin filaments) Intermediate filaments Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 6.26 0.25 µm • Microfilaments that function in cellular motility – Contain the protein myosin in addition to actin Muscle cell Actin filament Myosin filament Myosin arm Figure 6.27 A (a) Myosin motors in muscle cell contraction. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Amoeboid movement – Involves the contraction of actin and myosin filaments Cortex (outer cytoplasm): gel with actin network Inner cytoplasm: sol with actin subunits Extending pseudopodium Figure 6.27 B (b) Amoeboid movement Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Cytoplasmic streaming – Is another form of locomotion created by microfilaments Nonmoving cytoplasm (gel) Chloroplast Streaming cytoplasm (sol) Parallel actin filaments Figure 6.27 C (b) Cytoplasmic streaming in plant cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Cell wall Intermediate Filaments • Intermediate filaments – Support cell shape – Fix organelles in place Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Extracellular components and connections between cells help coordinate cellular activities • The cell wall – Is an extracellular structure of plant cells that distinguishes them from animal cells – Give support, but limit mobility • Plant cell walls = cellulose • Fungal cell walls = chitin Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Plant cell walls – Are made of cellulose fibers embedded in other polysaccharides and protein – May have multiple layers Central vacuole of cell Plasma membrane Secondary cell wall Primary cell wall Central vacuole of cell Middle lamella 1 µm Central vacuole Cytosol Plasma membrane Plant cell walls Figure 6.28 Plasmodesmata Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The Extracellular Matrix (ECM) of Animal Cells • Animal cells – Lack cell walls – Are covered by an elaborate matrix, the ECM Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The ECM – Is made up of glycoproteins and other macromolecules EXTRACELLULAR FLUID Collagen A proteoglycan complex Polysaccharide molecule Carbohydrates Core protein Fibronectin Plasma membrane Integrin Integrins Microfilaments Figure 6.29 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings CYTOPLASM Proteoglycan molecule • Functions of the ECM include – Support – Adhesion – Movement – Regulation Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Intercellular Junctions • A cell junction is a structure within a tissue of a multicellular organism. • Cell junctions are especially abundant in epithelial tissues. They consist of protein complexes and provide contact between neighboring cells, between a cell and the extracellular matrix, or they built up the paracellular barrier of epithelia and control the paracellular transport. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Plants: Plasmodesmata • Plasmodesmata – Are channels that perforate plant cell walls Cell walls Interior of cell Interior of cell Figure 6.30 0.5 µm Plasmodesmata Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Plasma membranes Animals: Tight Junctions, Desmosomes, and Gap Junctions • In animals, there are three types of intercellular junctions – Tight junctions – Desmosomes – Gap junctions •Invertebrates have several other types of specific junctions, for example Septate junctions or the CeAJ (C. elegans apical junction). Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Types of intercellular junctions in animals TIGHT JUNCTIONS Tight junction Tight junctions prevent fluid from moving across a layer of cells 0.5 µm At tight junctions, the membranes of neighboring cells are very tightly pressed against each other, bound together by specific proteins (purple). Forming continuous seals around the cells, tight junctions prevent leakage of extracellular fluid across A layer of epithelial cells. DESMOSOMES Desmosomes (also called anchoring junctions) function like rivets, fastening cells Together into strong sheets. Intermediate Filaments made of sturdy keratin proteins Anchor desmosomes in the cytoplasm. Tight junctions Intermediate filaments Desmosome Gap junctions Space between Plasma membranes cells of adjacent cells 1 µm Extracellular matrix Gap junction Figure 6.31 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 0.1 µm GAP JUNCTIONS Gap junctions (also called communicating junctions) provide cytoplasmic channels from one cell to an adjacent cell. Gap junctions consist of special membrane proteins that surround a pore through which ions, sugars, amino acids, and other small molecules may pass. Gap junctions are necessary for communication between cells in many types of tissues, including heart muscle and animal embryos. The Cell: A Living Unit Greater Than the Sum of Its Parts 5 µm • Cells rely on the integration of structures and organelles in order to function Figure 6.32 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings