several important scientists made plasma membrane...
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Chapter 2: Introduction to Cells
• Several important scientists made discoveries about cells • Robert Hooke • Matthias Schleiden and Theodor Schwann • Rudolf Virchow
• Cells—the smallest living units in our bodies • Organelles—“little organs”—carry on
essential functions of cells
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Introduction to Cells
• Cells have three main components • Plasma membrane—the outer boundary • Cytoplasm—contains most organelles • Nucleus—controls cellular activities
• NOTE: Important chemicals involved in cell anatomy include: • Water and ions (simple charged particles) • Macromolecules, such as…
• Proteins (chains of smaller units called amino acids) • Lipids (include fat [is 3 fatty acids + glycerol]; steroids; cholesterol;
waxes) • Carbohydrates (sugars: mono-saccharides, poly-saccharides,
glycogen) • ATP: adenosine triphosphate • Nucleic acids: DNA (deoxyribonucleic acid) and RNA (ribonucleic acid)
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Structure of a Generalized Cell
Figure 2.1
Secretion being released from cell by exocytosis
Peroxisome
Ribosomes
Rough endoplasmic reticulum
Nucleus
Nuclear envelope Chromatin
Golgi apparatus
Nucleolus
Smooth endoplasmic reticulum Cytosol
Lysosome
Mitochondrion
Centrioles
Centrosome matrix
Microtubule
Cytoskeletal elements
Intermediate filaments
Plasma membrane
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The Plasma Membrane
• Plasma membrane (or plasmalemma) defines the extent of the cell: separates intracellular fluid from extracellular fluid (watery inside from watery outside with a ‘fatty’ barrier)
• Structure of the cell membrane • Fluid mosaic model (lipid bilayer) • Types of membrane proteins
• Integral proteins—firmly imbedded in, or attached to lipid bilayer
• Short chains of carbohydrates attach to integral proteins • Form the glycocalyx
• Peripheral proteins—attach to membrane surface (in or out) • Support plasma membrane from the cytoplasmic side
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The Plasma Membrane
Figure 2.2
Integral proteins
Extracellular fluid (watery environment)
Cytoplasm (watery environment)
Polar head of phospholipid molecule
Glycolipid Cholesterol
Peripheral proteins
Bimolecular lipid layer containing proteins
Inward-facing layer of phospholipids
Outward- facing layer of phospholipids
Carbohydrate of glycocalyx
Glycoprotein Nonpolar tail of phospholipid molecule
Filament of cytoskeleton
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The Plasma Membrane
• Functions – relate to location at the interface of cell’s exterior and interior
• Provides barrier against substances outside cell • Some plasma membrane molecules act as receptors • Determines which substances enter or leave the cell
• Membrane is referred to as being “selectively permeable”
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Membrane Transport: moving substances across the cell membrane… These processes include:
• Simple diffusion—tendency of molecules to move down their concentration gradient through the lipid bilayer
• Osmosis—diffusion of water molecules across a membrane through small channels
• Facilitated diffusion—movement of molecules down their concentration gradient through an integral protein channel
• Active transport—integral proteins move molecules across the plasma membrane against their concentration gradient
• Endo- and exocytosis
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Figure 2.3 Membrane transport mechanisms.
Extracellular fluid
Lipid- soluble solutes
Water molecules
Lipid bilayer
Water soluble solutes Solute
ATP
Cytoplasm
Simple diffusion of fat-soluble molecules directly through the phospholipid bilayer down their concentration gradient
Osmosis, diffusion of water through the lipid bilayer and down its concentration gradient.
Facilitated diffusion An integral protein that spans the plasma membrane enables the passage of a particular solute across the membrane and down its conc gradient.
Active transport Some transport proteins use ATP as an energy source to actively pump substances across the plasma membrane against their concentration gradient.
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Endocytosis
• Endocytosis: Mechanism by which particles (chunks of stuff) enter cells • Phagocytosis—“cell eating” • Pinocytosis—“cell drinking”
• Receptor-mediated endocytosis • Plasma proteins bind to certain molecules • Invaginates and forms a coated pit
• Pinches off to become a coated vesicle • NOTE: This is the method by which insulin and
cholesterol and some viruses enter cells!
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Three Types of Endocytosis
Figure 2.4
Phagosome
Vesicle
Vesicle
Receptor recycled to plasma membrane
(a) Phagocytosis The cell engulfs a large particle by forming pro- jecting pseudopods (”false feet”) around it and en- closing it within a membrane sac called a phagosome. The phagosome then combines with a lysosome, and its contents are digested. Vesicle may or may not be protein-coated but has receptors capable of binding to microorganisms or solid particles.
(b) Pinocytosis The cell “gulps” drops of extracellular fluid containing solutes into tiny vesicles. No receptors are used, so the process is nonspecific. Most vesicles are protein- coated.
(c) Receptor-mediated endocytosis Extracellular substances bind to specific receptor proteins in regions of protein-coated pits, enabling the cell to ingest and concentrate specific substances in protein-coated vesicles. The ingested substance may simply be released inside the cell, or combined with a lysosome to digest contents. Receptors are recycled to the plasma membrane in vesicles.
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Exocytosis
• Exocytosis—a mechanism that moves substances out of the cell • Substance is enclosed in a vesicle • The vesicle migrates to the plasma membrane • Proteins from the vesicles (v-SNAREs) bind with
membrane proteins (t-SNAREs) • The lipid layers from both membranes bind, and the
vesicle releases its contents to the outside of the cell
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Exocytosis
Figure 2.5
The membrane- bound vesicle migrates to the plasma membrane.
There, proteins at the vesicle surface (v-SNAREs) bind with t-SNAREs (plasma membrane proteins).
The vesicle and plasma membrane fuse and a pore opens up.
Vesicle contents are released to the cell exterior.
(a) The process of exocytosis Extracellular
fluid Plasma membrane SNARE (t-SNARE)
Secretory vesicle Vesicle SNARE
(v-SNARE) Molecule to be secreted
Cytoplasm
Fused v- and t-SNAREs
Fusion pore formed
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The Cytoplasm
• Cytoplasm—lies internal to plasma membrane • Consists of cytosol, organelles, and inclusions, in
watery environment
• Cytosol • Jelly-like watery fluid in which other cellular elements
are suspended • Consists of water with dissolved ions (salts) and
enzymes
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Cytoplasmic Organelles • Ribosomes—constructed of proteins and ribosomal
RNA; not surrounded by a membrane • Site of protein synthesis
• Assembly of proteins is a process called translation
• Are the “assembly line” of the manufacturing plant
• Endoplasmic reticulum—“network within the cytoplasm”– tow types of ER: • Rough ER—ribosomes stud the external surfaces, so
protein synthesis occurs here • Smooth ER—consists of tubules in a branching
network; No ribosomes are attached, therefore no protein synthesis—but lipid and carb synthesis
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The Endoplasmic Reticulum and Ribosomes
Figure 2.6
Nuclear envelope
Ribosomes
Rough ER
(a) Diagrammatic view of smooth and rough ER
Smooth ER
(b) Electron micrograph of smooth and rough ER (85,000×)
Cisternae
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Cytoplasmic Organelles
• Golgi apparatus—a stack of three to 10 disk-shaped envelopes • Sorts products of rough ER and sends them to proper
destination • Products of rough ER move through the Golgi from
the convex (cis) to the concave (trans) side • Is the “packaging and shipping” division of the
manufacturing plant
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Golgi Appartus
Cis face— “receiving” side of Golgi apparatus
Secretory vesicle
(a) Many vesicles in the process of pinching off from the membranous Golgi apparatus
(b) Electron micrograph of the Golgi apparatus (90,000×)
Transport vesicle from the Golgi apparatus
Transport vesicle from trans face
Trans face— “shipping” side of Golgi apparatus
New vesicles forming
New vesicles forming
Cisternae Transport vesicle from rough ER
Golgi apparatus
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Plasma membrane
Secretion by exocytosis
Vesicle becomes lysosome
Golgi apparatus
Rough ER ER membrane Phagosome Proteins in cisterna
Pathway B: Vesicle membrane to be incorporated into plasma membrane Pathway A:
Vesicle contents destined for exocytosis Extracellular fluid
Secretory vesicle
Pathway C: Lysosome containing acid hydrolase enzymes
Protein-containing vesicles pinch off rough ER and migrate to fuse with membranes of Golgi apparatus.
Proteins are modified within the Golgi compartments.
Proteins are then packaged within different vesicle types, depending on their ultimate destination.
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The sequence of events from protein synthesis on the rough ER to the final distribution of these proteins (1 of 2).
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More Cytoplasmic Organelles...
• Lysosomes—membrane-walled sacs containing digestive enzymes • Digest unwanted substances
• Peroxisomes—membrane-walled sacs of oxidase enzymes • Enzymes neutralize free radicals and break down
poisons • Break down long chains of fatty acids • Are numerous in the liver and kidneys • Are the toxic waste removal system
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Lysosomes
Light areas are regions where materials are being digested.
Figure 2.9
Lysosomes
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Mitochondria
• Mitochondria—generate most of the cell’s energy
• most complex organelle • Contain some maternally inherited DNA • Believed to have arisen from bacteria
• More abundant in energy-requiring cells, like muscle cells and sperm
• “Power plant” of the cell: release energy stored in chemical bonds and transfer energy to produce ATP
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Figure 2.10 Mitochondria.
Outer mitochondrial
membrane Ribosome
Inner mitochondrial membrane Cristae
Matrix
Mitochondrial DNA
Enzymes
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More Cytoplasmic Organelles
• Cytoskeleton—“cell skeleton”—an elaborate network of rods: for support and communication
• Contains three types of rods: • Microtubules—cylindrical structures made of
proteins • Microfilaments—filaments of contractile protein
actin • Intermediate filaments—protein fibers
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Cytoskeleton: Microfilaments
Figure 2.11a
(a) Microfilaments
Strands made of spherical protein subunits called actins
Actin subunit
7 nm
Microfilaments form the blue network surrounding the pink nucleus in this photo.
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Cytoskeleton: Intermediate filaments
Figure 2.11b
(b) Intermediate filaments
Tough, insoluble protein fibers constructed like woven ropes
10 nm
Fibrous subunits
Intermediate filaments form the purple batlike network in this photo.
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Cytoskeleton: Microtubules
Figure 2.11c
(c) Microtubules
Hollow tubes of spherical protein subunits called tubulins
25 nm
Tubulin subunits
Microtubules appear as gold networks surrounding the cells’ pink nuclei in this photo.
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More Cytoplasmic Organelles...
• Centrosomes and centrioles
• Centrosome—a spherical structure in the cytoplasm • Composed of centrosome matrix and centrioles
• Centrioles—paired cylindrical bodies • Consists of 27 short microtubules • Act in forming cilia • Necessary for karyokinesis (nuclear division)
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Cytoplasmic Inclusions
• Temporary structures • Not present in all cell types
• May consist of pigments, crystals of protein, and food stores; examples ... • Lipid droplets—found in liver cell and fat cells • Glycosomes—store sugar in the form of glycogen
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The Nucleus • The nucleus—“little nut” or “kernel”: control center of
cell • DNA directs the cell’s activities– provides instructions for
protein synthesis • Nucleus is approximate 5µm in diameter
• Nuclear envelope—two parallel membranes separated by fluid-filled space
• Nuclear pores --- penetrate the nuclear envelope • Pores allow large molecules to pass in and out of
the nucleus • Nucleolus—“little nucleus”—in the center of the nucleus
• Contains parts of several chromosomes • Site of ribosome subunit assembly
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The Nucleus
Figure 2.13
Chromatin (condensed)
Nuclear envelope Nucleus Nuclear pores
Fracture line of outer membrane
Nuclear pore complexes. Each pore is ringed by protein particles
Surface of nuclear envelope.
Nuclear lamina. The netlike lamina composed of intermediate filaments formed by lamins lines the inner surface of the nuclear envelope.
Nucleolus
Cisternae of rough ER (a)
(b)
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Chromatin and Chromosomes
• DNA (NOT a protein but another type of macromolecule called a nucleic acid) is a double helix is composed of four subunits: • Thymine (T), adenine (A), cytosine (C), and guanine (G)
• DNA is packed with protein molecules • DNA plus the proteins form chromatin (“colored
stuff”) • Each cluster of DNA and histone proteins is a
nucleosome
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Chromatin and Chromosomes
The double-helix structure of the
DNA molecule:
Deoxyribose sugar Phosphate
Sugar-phosphate backbone
Hydrogen bond
Adenine (A) Thymine (T) Cytosine (C) Guanine (G)
Nucleotides
Figure 2.14
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Chromatin and Chromosomes
• Extended chromatin • Is the active region of DNA where DNA’s genetic
code is copied onto mRNA (transcription)
• Condensed chromatin • Tightly coiled nucleosomes • Inactive form of chromatin
• Chromosomes—highest level of organization of chromatin • Contains a long molecule of DNA
• 46 chromosomes (arranged in 23 pairs) are in a typical human cell
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Metaphase chromosome (at midpoint of cell division)
Nucleosome (10-nm diameter; eight histone proteins wrapped by two winds of the DNA double helix)
Linker DNA
Histones
(a)
(b)
DNA double helix (2-nm diameter)
Chromatin (“beads on a string”) structure with nucleosomes
Tight helical fiber (30-nm diameter)
Chromatid (700-nm diameter)
Looped domain structure (300-nm diameter)
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2
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Figure 2.15
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The Cell Life Cycle • The cell life cycle is the series of changes a cell
goes through • Interphase
• G1 phase—growth 1 or Gap 1 phase • The first part of interphase • Cell metabolically active—growth—make proteins • Variable in length from hours to YEARS (egg cell) • Centrioles begin to replicate near the end of G1
• S (synthetic) phase—DNA replicates itself • Ensures that daughter cells receive identical copies of the
genetic material (chromatin extended) • G2 phase—growth 2 or Gap 2 • Centrioles finish copying themselves • Enzymes needed for cell division are synthesized in G2
• During S (synthetic) and G2 phases, cell carries on normal activities
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G1 Growth
S Growth and DNA
synthesis G2 Growth and final preparations for
division M
G2 checkpoint
G1 checkpoint (restriction point)
Mitotic phase (M)
Cytokinesis
Telophase
Anaphase
Metaphase
Prophase
Interphase
Mitosis
The Cell Life Cycle
Figure 2.16
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The Cell Life Cycle
• Cell division • M (mitotic) phase—cells divide during this stage
• Follows interphase (G1, S, and G2)
• Cell division involves: • Mitosis—division of the nucleus during cell division
• Chromosomes are distributed to the two daughter nuclei
• Cytokinesis—division of the cytoplasm • Occurs after the nucleus divides
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The Stages of Mitosis • Prophase—the first and longest stage of
mitosis • Early prophase—chromatin threads condense into
chromosomes • Chromosomes are made up of two threads called
chromatids (sister chromatids) • Chromatids are held together by the centromere • Centriole pairs separate from one another • The mitotic spindle forms
• Late prophase—centrioles continue moving away from each other • Nuclear membrane fragments
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Early Prophase and Late Prophase
Figure 2.17 (1 of 2)
Centrosomes (each has 2 centrioles)
Early mitotic spindle Spindle pole
Kinetochore Kinetochore microtubule
Polar microtubule
Nucleolus Centromere
Plasma membrane Fragments
of nuclear envelope Aster
Nuclear envelope
Chromosome consisting of two sister chromatids
Chromatin
Interphase Early Prophase Late Prophase
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The Stages of Mitosis
• Metaphase—the second stage of mitosis • Chromosomes cluster at the middle of the cell
• Centromeres are aligned along the equator
• Anaphase—the third and shortest stage of mitosis • Centromeres of chromosomes split
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Metaphase and Anaphase
Figure 2.17 (2 of 2)
Contractile ring at cleavage furrow
Nuclear envelope forming
Nucleolus forming Spindle
Metaphase plate Daughter
chromosomes
Metaphase Anaphase Telophase and Cytokinesis
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The Stages of Mitosis
• Telophase begins as chromosomal movement stops • Chromosomes at opposite poles of the cell uncoil • Resume threadlike extended-chromatin form • A new nuclear membrane forms
• Cytokinesis completes the division of the cell into two daughter cells
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Contractile ring at cleavage furrow
Nuclear envelope forming
Nucleolus forming Spindle
Metaphase plate Daughter
chromosomes
Metaphase Anaphase Telophase and Cytokinesis
Telophase and Cytokinesis
Figure 2.17 Copyright © 2011 Pearson Education, Inc. Copyright © 2011 Pearson Education, Inc.
Cellular Diversity
• Specialized functions of cells relates to: • Shape of cell • Arrangement of organelles
Some types of cells… • 1. Cells that connect body parts or cover
organs or transport gases • Fibroblast—makes and secretes protein component
of fibers • Erythrocyte—concave shape provides surface area
for uptake of the respiratory gases • Epithelial cell—hexagonal shape allows maximum
number of epithelial cells to pack together
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Cells that Connect Body Parts or Cover Organs
Figure 2.18a
Fibroblasts
Erythrocytes
Epithelial cells
(a) Cells that connect body parts, form linings, or transport gases
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Cellular Diversity
• 2. Cells that move organs and body parts • Skeletal and smooth muscle cells
• Elongated and filled with actin and myosin • Contract forcefully (”shorten with force”)
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Cells that Connect Organs and Body Parts
Figure 2.18b
(b) Cells that move organs and body parts
Skeletal muscle cell
Smooth muscle cells
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Cellular Diversity
• 3. Cells that store nutrients • Fat cell—shape is produced by large fat droplet in its
cytoplasm
• 4. Cells that fight disease • Macrophage—moves through tissue to reach
infection sites
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Cells that Store Nutrients and Cells that Fight Disease
Figure 2.18c, d
(d) Cell that fights disease
Macrophage (c) Cell that stores nutrients
Fat cell
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Cellular Diversity
• 5. Cells that gather and process information • Neuron—has long processes for receiving and
transmitting messages
Figure 2.18e
Nerve cell
(e) Cell that gathers information and controls body functions
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Cellular Diversity
• 6. Cells of reproduction • Sperm (male) – possesses long tail for swimming to
the egg for fertilization
Figure 2.18f
Sperm
(f) Cell of reproduction
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Developmental Aspects of Cells
• Aging—a complex process caused by a variety of factors
• Free radical theory • Damage from byproducts of cellular metabolism • Radicals build up and damage essential molecules of cells
• Mitochondrial theory • A decrease in production of energy by mitochondria weakens
and ages our cells
• Genetic theory proposes that aging is programmed by genes • Telomeres—“end caps” on chromosomes • Telomerase—prevents telomeres from degrading