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EXPLORING LIFE & A TOUR OF THE CELL Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 1 Exploring Life • Biology – Is the scientific study of life • We recognize life – By what living things do Figure 1.1 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 2 Some properties of life (a) Order (b) Evolutionary adaptation (c) Response to the environment (d) Regulation (e) Energy processing (f) Growth and development Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings (g) Reproduction I-1- 3 From the biosphere to organisms 1 The biosphere Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 4 From cells to molecules 9 Organelles 1 µm Cell 8 Cells Atoms 10 µm 10 Molecules 7 Tissues 50 µm 6 Organs and organ systems Figure 1.3 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 5 A Closer Look at Ecosystems • Each organism – Interacts with its environment • Both organism and environment – Are affected by the interactions between them Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 6 A Closer Look at Cells • The cell – Is the lowest level of organization that can perform all activities required for life Figure 1.5 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 25 µm I-1- 7 The Cell’s Heritable Information • Cells contain chromosomes made partly of DNA, the substance of genes – Which program the cells’ production of proteins and transmit information from parents to offspring Sperm cell Nuclei containing DNA Egg cell Fertilized egg with DNA from both parents Figure 1.6 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Embyro’s cells with copies of inherited DNA Offspring with traits inherited from both parents I-1- 8 The molecular structure of DNA • Accounts for it information-rich nature Nucleus DNA Cell Nucleotide Figure 1.7 (a) DNA double helix. This model shows each atom in a segment of DNA.Made up of two long chains of building blocks called nucleotides, a DNA molecule takes the three-dimensional form of a double helix. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings A C T A T A C C G T A G T A (b) Single strand of DNA. These geometric shapes and letters are simple symbols for the nucleotides in a small section of one chain of a DNA molecule. Genetic information is encoded in specific sequences of the four types of nucleotides (their names are abbreviated here as A, T, C, and G). I-1- 9 Two Main Forms of Cells • All cells share certain characteristics – They are all enclosed by a membrane – They all use DNA as genetic information • There are two main forms of cells – Eukaryotic – Prokaryotic Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 10 • Eukaryotic cells – Are subdivided by internal membranes into various membrane-enclosed organelles • Prokaryotic cells – Lack the kinds of membrane-enclosed organelles found in eukaryotic cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 11 EUKARYOTIC CELL PROKARYOTIC CELL DNA Membrane (no nucleus) Membrane Cytoplasm Organelles Figure 1.8 Nucleus (contains DNA) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 1 µm I-1- 12 Biologists explore life across its great diversity of species • Diversity is a hallmark of life Figure 1.13 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 13 Grouping Species: The Basic Idea • Taxonomy – Is the branch of biology that names and classifies species according to a system of broader and broader groups Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 14 Classifying life Species Genus Family Order Class Phylum Kingdom Domain Ursus americanus (American black bear) Ursus Ursidae Carnivora Mammalia Chordata Animalia Figure 1.14 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Eukarya I-1- 15 The Three Domains of Life • At the highest level, life is classified into three domains – Bacteria – Archaea – Eukarya • Domain Bacteria and domain Archaea – Consist of prokaryotes • Domain Eukarya, the eukaryotes – Includes the various protist kingdoms and the kingdoms Plantae, Fungi, and Animalia Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 16 Life’s three domains Bacteria are the most diverse 4 µm and widespread prokaryotes and are now divided among multiple kingdoms. Each of the rod-shaped structures in this photo is a bacterial cell. DOMAIN ARCHAEA Figure 1.15 Many of the prokaryotes known 0.5 µm as archaea live in Earth‘s extreme environments, such as salty lakes and boiling hot springs. Domain Archaea includes multiple kingdoms. The photo shows a colony composed of many cells. Protists (multiple kingdoms) 100 µm are unicellular eukaryotes and their relatively simple multicellular relatives.Pictured here is an assortment of protists inhabiting pond water. Scientists are currently debating how to split the protists into several kingdoms that better represent evolution and diversity. Kingdom Plantae consists of multicellula eukaryotes that carry out photosynthesis, the conversion of light energy to food. Kindom Fungi is defined in part by the nutritional mode of its members, such as this mushroom, which absorb nutrientsafter decomposing organic material. Kindom Animalia consists of multicellular eukaryotes that ingest other organisms. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 17 Unity in the Diversity of Life • As diverse as life is – There is also evidence of remarkable unity 15 µm 1.0 µm Cilia of Paramecium. The cilia of Paramecium propel the cell through pond water. 5 µm Cross section of cilium, as viewed with an electron microscope Cilia of windpipe cells. The cells that line the human windpipe are equipped with cilia that help keep the lungs clean by moving a film of debris-trapping mucus upward. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 18 A Tour of the Cell Overview: The Importance of Cells • All organisms are made of cells • The cell is the simplest collection of matter that can live Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 19 Cell structure is correlated to cellular function 10 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 20 To study cells, biologists use microscopes and the tools of biochemistry 1m Human height Length of some nerve and muscle cells 0.1 m Chicken egg 1 cm Frog egg 1 mm Most plant and Animal cells 10 µ 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nucleus Most bacteria Mitochondrion 1µm Smallest bacteria 100 nm Viruses 10 nm Ribosomes Electron microscope 100 µm Electron microscope – Can be used to visualize different sized cellular structures Light microscope • Different types of microscopes Unaided eye 10 m Proteins 1 nm Lipids Small molecules 0.1 nm Atoms I-1- 21 Use different methods for enhancing visualization of cellular structures TECHNIQUE RESULT (a) Brightfield (unstained specimen). Passes light directly through specimen. Unless cell is naturally pigmented or artificially stained, image has little contrast. [Parts (a)–(d) show a human cheek epithelial cell.] 50 µm (b) Brightfield (stained specimen). Staining with various dyes enhances contrast, but most staining procedures require that cells be fixed (preserved). (c) Phase-contrast. Enhances contrast in unstained cells by amplifying variations in density within specimen; especially useful for examining living, unpigmented cells. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 22 (d) Differential-interference-contrast (Nomarski). Like phase-contrast microscopy, it uses optical modifications to exaggerate differences in density, making the image appear almost 3D. (e) Fluorescence. Shows the locations of specific molecules in the cell by tagging the molecules with fluorescent dyes or antibodies. These fluorescent substances absorb ultraviolet radiation and emit visible light, as shown here in a cell from an artery. 50 µm (f) Confocal. Uses lasers and special optics for “optical sectioning” of fluorescently-stained specimens. Only a single plane of focus is illuminated; out-of-focus fluorescence above and below the plane is subtracted by a computer. A sharp image results, as seen in stained nervous tissue (top), where nerve cells are green, support cells are red, and regions of overlap are yellow. A standard fluorescence micrograph (bottom) of this relatively thick tissue is blurry. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-150 µm23 Electron microscopes (EMs) • 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. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 24 The transmission electron microscope (TEM) • Provides for detailed study of the internal ultrastructure of cells Longitudinal section of cilium Cross section of cilium 1 µm (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. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 25 Isolating Organelles by Cell Fractionation Homogenization Tissue cells 1000 g (1000 times the force of gravity) 10 min Homogenate Differential centrifugation Supernatant poured into next tube 20,000 g 20 min 80,000 g 60 min Pellet rich in nuclei and cellular debris 150,000 g 3 hr Pellet rich in mitochondria (and chloroplasts if cells are from a plant) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Pellet rich in “microsomes” (pieces of plasma membranes and cells’ internal membranes) Pellet rich in ribosomes I-1- 26 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 I-1- 27 Prokaryotic cells: Do not contain a nucleus; Have their DNA located in a region called the nucleoid. 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 Plasma membrane: membrane enclosing the cytoplasm Cell wall: rigid structure outside the plasma membrane Bacterial chromosome (a) A typical rod-shaped bacterium Capsule: jelly-like outer coating of many prokaryotes 0.5 µm Flagella: locomotion organelles of some bacteria Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings (b) A thin section through the bacterium Bacillus coagulans (TEM) I-1- 28 Eukaryotic cells: Contain a true nucleus, bounded by a membranous nuclear envelope; Are generally quite a bit bigger than prokaryotic cells • The plasma membrane: Functions as a selective barrier Outside of cell Allows sufficient passage of nutrients and waste Carbohydrate side chain Hydrophilic region Inside of cell 0.1 µm Hydrophobic region (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 I-1- 29 • A animal cell ENDOPLASMIC RETICULUM (ER) Rough ER Smooth ER Nuclear envelope NUCLEUS Nucleolus Chromatin Flagelium Plasma membrane Centrosome CYTOSKELETON Microfilaments Intermediate filaments Ribosomes Microtubules Microvilli Golgi apparatus Peroxisome Copyright © 2005 Pearson Education, Inc.Mitochondrion publishing as Benjamin Cummings Lysosome In animal cells but not plant cells: Lysosomes Centrioles Flagella (in some plant sperm) I-1- 30 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings In plant cells but not animal cells: Chloroplasts Central vacuole and tonoplast Cell wall Plasmodesmata I-1- 31 Concept : The eukaryotic cell’s genetic instructions are housed in the nucleus and carried out by the ribosomes • The Nucleus: Genetic Library of the Cell • The nucleus – Contains most of the genes in the eukaryotic cell Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 32 The nuclear envelope • Encloses the nucleus, separating its contents from the Nucleus cytoplasm Nucleus 1 µm Nucleolus Chromatin 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 Pore complexes (TEM). Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nuclear lamina (TEM). I-1- 33 Ribosomes: Protein Factories in the Cell – Are particles made of ribosomal RNA and protein; Carry out protein synthesis Ribosomes ER Cytosol Endoplasmic reticulum (ER) Free ribosomes Bound ribosomes Large subunit 0.5 µm TEM showing ER and ribosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Small subunit Diagram of a ribosome I-1- 34 Concept : 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 I-1- 35 The Endoplasmic Reticulum: Biosynthetic Factory Accounts for more than half the total membrane in many eukaryotic cells • The ER membrane Is continuous with the nuclear envelope Smooth ER Rough ER ER lumen Cisternae Ribosomes Transport vesicle Smooth ER Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Nuclear envelope Transitional ER Rough ER 200 µm I-1- 36 There are two distinct regions of ER – Smooth ER, which lacks ribosomes – Rough ER, which contains ribosomes • The smooth ER: Synthesizes lipids; Metabolizes carbohydrates; Stores calcium; Detoxifies poison • 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 I-1- 37 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 I-1- 38 Functions of the Golgi apparatus cis face (“receiving” side of Golgi apparatus) Golgi apparatus 6 Vesicles also transport certain proteins back to ER 1 Vesicles move from ER to Golgi 5 Vesicles transport specific proteins backward to newer Golgi cisternae 2 Vesicles coalesce to form new cis Golgi cisternae 0.1 0 µm Cisternae 3 Cisternal maturation: Golgi cisternae move in a cisto-trans direction 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 TEM of Golgi apparatus I-1- 39 Lysosomes: Digestive Compartments Membranous sac of hydrolytic enzymes; Can digest all kinds of macromolecules 1 µm Nucleus • Carry out intracellular • digestion by • phagocytosis Lysosome Lysosome contains active hydrolytic enzymes Food vacuole fuses with lysosome Hydrolytic enzymes digest food particles Digestive enzymes Lysosome Plasma membrane Digestion Figure 6.14 A Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Food vacuole (a) Phagocytosis: lysosome digesting food I-1- 40 Vacuoles: Diverse Maintenance Compartments • A plant or fungal cell – May have one or several vacuoles • Food vacuoles – Are formed by phagocytosis • Contractile vacuoles – Pump excess water out of protist cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 41 • 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 5 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 42 The Endomembrane System: A Review • 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 3 Membranes and proteins produced by the ER flow in the form of transport vesicles to the Golgi Smooth ER cis Golgi Nuclear envelop 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 5 Transport vesicle carries proteins to plasma membrane for secretion 6 Plasma membrane expands by fusion of vesicles; proteins are secreted from cell I-1- 43 Concept: 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 I-1- 44 Mitochondria: Chemical Energy Conversion • Are found in nearly all eukaryotic cells • Mitochondria are enclosed by two membranes – 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 Mitochondrial DNA Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 100 µm I-1- 45 Chloroplasts: Capture of Light Energy • The chloroplast is a specialized member of a family of closely related plant organelles called plastids – Contains chlorophyll; Are found in leaves and other green organs of plants and in algae Chloroplast Ribosomes Stroma Chloroplast DNA Inner and outer membranes Granum 1 µm Thylakoid Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 46 Peroxisomes: Oxidation – Produce hydrogen peroxide and convert it to water Chloroplast Peroxisome Mitochondrion 1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 47 Concept: The cytoskeleton is a network of fibers that organizes structures and activities in the cell • Cytoskeleton is a network of fibers extending throughout the cytoplasm Microtubule 0.25 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Microfilaments I-1- 48 Roles of the Cytoskeleton: Support, Motility, and Regulation – Is involved in cell motility, which utilizes motor proteins ATP Vesicle Receptor for motor protein Motor protein Microtubule (ATP powered) of cytoskeleton (a) Motor proteins that attach to receptors on organelles can “walk” the organelles along microtubules or, in some cases, microfilaments. Vesicles Microtubule 0.25 µm (b) Vesicles containing neurotransmitters migrate to the tips of nerve cell axons via the mechanism in (a). In this SEM of a squid giant axon, two vesicles can be seen moving along a microtubule. (A separate part of the experiment provided the evidence that they were in fact moving.) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 49 Components of the Cytoskeleton • There are three main types of fibers that make up the cytoskeleton Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 50 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 I-1- 51 Centrosomes and Centrioles • The centrosome is considered to be a “microtubule- organizing center”; Contains a pair of centrioles Centrosome Microtubule Centrioles 0.25 µm Figure 6.22 Longitudinal section of one centriole Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Microtubules Cross section of the other centriole I-1- 52 Cilia and Flagella – Contain specialized arrangements of microtubules – Are locomotor appendages of some cells Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 53 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 1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 54 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). 15 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 55 Cilia and flagella share a common ultrastructure Outer microtubule doublet Dynein arms 0.1 µm Plasma membrane 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) Cross section of basal body Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 56 Microfilaments (Actin Filaments) – Are built from molecules of the protein actin – Are found in microvilli Microvillus Plasma membrane Microfilaments (actin filaments) Intermediate filaments 0.25 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 57 Microfilaments that function in cellular motility • Contain the protein myosin in addition to actin Muscle cell Actin filament Myosin filament Myosin arm (a) Myosin motors in muscle cell contraction. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 58 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 (b) Amoeboid movement Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 59 Cell Walls of Plants – Is an extracellular structure of plant cells that distinguishes them from animal cells – 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Plasmodesmata I-1- 60 The Extracellular Matrix (ECM) of Animal Cells • Animal cells lack cell walls and covered by an elaborate matrix, 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Proteoglycan molecule CYTOPLASM I-1- 61 Functions of the ECM include – Support – Adhesion – Movement – Regulation Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 62 Intercellular Junctions – Plants: Plasmodesmata – Are channels that perforate plant cell walls Cell walls Interior of cell Interior of cell 0.5 µm Plasmodesmata Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Plasma membranes I-1- 63 Animals: Tight Junctions, Desmosomes, and Gap Junctions • In animals, there are three types of intercellular junctions – Tight junctions – Desmosomes – Gap junctions Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 64 • 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 0.1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 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. I-1- 65 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 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings I-1- 66