chapter 2 218/martini ppt...chapter 2 foundations the cell ... •glycolipids and glycoproteins form...
TRANSCRIPT
Lecture Presentation by
Steven Bassett
Southeast Community College
Chapter 2
Foundations
The Cell
© 2015 Pearson Education, Inc.
Introduction
• There are trillions of cells in the body
• Cells are the structural “building blocks” of all
plants and animals
• Cells are produced by the division of preexisting
cells
• Cells form all the structures in the body
• Cells perform all vital functions of the body
© 2015 Pearson Education, Inc.
Introduction
• There are two types of cells in the body:
• Sex cells
• Sperm in males and oocytes in females
• Somatic cells
• All the other cells in the body that are not sex cells
© 2015 Pearson Education, Inc.
Cellular Anatomy
• The cell consists of:
• Cytoplasm
• Cytosol
• Organelles
• Plasmalemma
• Cell membrane
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Figure 2.2 A Flowchart for the Study of Cell Structure
© 2015 Pearson Education, Inc.
The Cell
Plasmalemma
Cytoplasm
Cytosol Organelles
Nonmembranous
Organelles
Membranous
Organelles
can be divided
into
Divided into
subdivided into
• Cytoskeleton
• Microvilli
• Centrioles
• Cilia
• Flagella
• Ribosomes
• Mitochondria
• Nucleus
• Endoplasmic
reticulum
• Golgi apparatus
• Lysosomes
• Peroxisomes
Cellular Anatomy
• Anatomical Structures of the Cell
• Organelles
• Nonmembranous organelles
• Membranous organelles
© 2015 Pearson Education, Inc.
Cellular Anatomy
• Organelles of the Cell
• Nonmembranous organelles
• Cytoskeleton
• Microvilli
• Centrioles
• Cilia
• Flagella
• Ribosomes
© 2015 Pearson Education, Inc.
Table 2.1 Anatomy of a Representative Cell (1 of 2)
© 2015 Pearson Education, Inc.
Figure 2.1 Anatomy of a Typical Cell
© 2015 Pearson Education, Inc.
Microvilli
Secretory vesicles
Cytosol
Lysosome
Centrosome
Centriole
Chromatin
Nucleoplasm
Nucleolus
Nuclear envelope surrounding nucleus
Cytoskeleton
Plasmalemma Free ribosomes
Fixed ribosomes
Rough endoplasmic reticulum
Smooth endoplasmic reticulum
Nuclear pores
Peroxisome
Mitochondrion
Golgi apparatus
Cellular Anatomy
• Organelles of the Cell
• Membranous organelles
• Mitochondria
• Nucleus
• Endoplasmic reticulum
• Golgi apparatus
• Lysosomes
• Peroxisomes
© 2015 Pearson Education, Inc.
Table 2.1 Anatomy of a Representative Cell (2 of 2)
© 2015 Pearson Education, Inc.
Figure 2.1 Anatomy of a Typical Cell
© 2015 Pearson Education, Inc.
Microvilli
Secretory vesicles
Cytosol
Lysosome
Centrosome
Centriole
Chromatin
Nucleoplasm
Nucleolus
Nuclear envelope surrounding nucleus
Cytoskeleton
Plasmalemma Free ribosomes
Fixed ribosomes
Rough endoplasmic reticulum
Smooth endoplasmic reticulum
Nuclear pores
Peroxisome
Mitochondrion
Golgi apparatus
Cellular Anatomy
• Plasmalemma
• A cell membrane composed of:
• Phospholipids
• Glycolipids
• Protein
• Cholesterol
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Table 2.1 Anatomy of a Representative Cell (1 of 2)
© 2015 Pearson Education, Inc.
Figure 2.3 The Plasmalemma
© 2015 Pearson Education, Inc.
Hydrophilic
heads
a
b
Hydrophobic
tails
Cholesterol
Glycolipids of glycocalyx
Phospholipid bilayer
Integral protein with channel
Hydrophobic tails
Integral glycoproteins
Cytoskeleton (Microfilaments)
Hydrophilic heads
Peripheral proteins
Cholesterol
Gated channel
CYTOPLASM
= 2 nm
EXTRACELLULAR FLUID
The phospholipid
bilayer
The plasmalemma
Cellular Anatomy
• Functions of the Plasmalemma
• Cell membrane (also called phospholipid
bilayer)
• Major functions:
• Physical isolation
• Regulation of exchange with the environment
(permeability)
• Sensitivity
• Cell-to-cell communication/Adhesion/Structural
support
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Cellular Anatomy
• Structure of the Plasmalemma
• Called a phospholipid bilayer
• Composed of two layers of phospholipid
• Hydrophobic heads are at the surfaces (inside lining
and outside lining)
• Hydrophilic fatty acids (tails) “face toward each
other”
• Outer layer consists of glycolipids and glycoproteins
• Glycolipids and glycoproteins form a glycocalyx
coating
• Inner layer does not consist of glycolipids or
glycoproteins
© 2015 Pearson Education, Inc.
Figure 2.3 The Plasmalemma
© 2015 Pearson Education, Inc.
Hydrophilic
heads
a
b
Hydrophobic
tails
Cholesterol
Glycolipids of glycocalyx
Phospholipid bilayer
Integral protein with channel
Hydrophobic tails
Integral glycoproteins
Cytoskeleton (Microfilaments)
Hydrophilic heads
Peripheral proteins
Cholesterol
Gated channel
CYTOPLASM
= 2 nm
EXTRACELLULAR FLUID
The phospholipid
bilayer
The plasmalemma
Cellular Anatomy
• Structure of the Plasmalemma
• Composed of protein molecules
• Peripheral proteins: attached to the glycerol
portions of the fatty acids
• Integral proteins: embedded within the cell
membrane
• Form channels such as gated channels
• Channels open and close
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Figure 2.3 The Plasmalemma
© 2015 Pearson Education, Inc.
Hydrophilic
heads
a
b
Hydrophobic
tails
Cholesterol
Glycolipids of glycocalyx
Phospholipid bilayer
Integral protein with channel
Hydrophobic tails
Integral glycoproteins
Cytoskeleton (Microfilaments)
Hydrophilic heads
Peripheral proteins
Cholesterol
Gated channel
CYTOPLASM
= 2 nm
EXTRACELLULAR FLUID
The phospholipid
bilayer
The plasmalemma
Cellular Anatomy
• Structure of the Plasmalemma
• Composed of sterol molecules
• Function to maintain fluidity of the membrane
• An example is cholesterol
© 2015 Pearson Education, Inc.
Figure 2.3 The Plasmalemma
© 2015 Pearson Education, Inc.
Hydrophilic
heads
a
b
Hydrophobic
tails
Cholesterol
Glycolipids of glycocalyx
Phospholipid bilayer
Integral protein with channel
Hydrophobic tails
Integral glycoproteins
Cytoskeleton (Microfilaments)
Hydrophilic heads
Peripheral proteins
Cholesterol
Gated channel
CYTOPLASM
= 2 nm
EXTRACELLULAR FLUID
The phospholipid
bilayer
The plasmalemma
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Passive processes
• Diffusion
• Osmosis
• Facilitative diffusion
• Active processes
• Active transport
• Endocytosis
• Exocytosis
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Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Passive process: diffusion
• Movement of molecules from an area of high
concentration to an area of low concentration
• Permeablity, concentration gradient, molecule size
and charge, temperature affect the rate of
movement
• Small inorganic ions and small molecules are
involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (1 of 6)
© 2015 Pearson Education, Inc.
Plasmalemma
Diffusion
CO2 Extracellular
fluid
Example:
When the concentration of CO2
inside a cell is greater than outside
the cell, CO2 diffuses out of the cell
and into the extracellular fluid.
Diffusion is the movement of molecules
from an area of higher concentration to an
area of lower concentration. The difference
between the high and low concentrations is
a concentration gradient. In diffusion,
molecules move down a concentration
gradient until the gradient is eliminated.
Factors Affecting Rate:
Membrane permeability; magnitude of the
concentration gradient; size, charge, and
lipid solubility of the diffusing molecules;
presence of membrane channel proteins;
temperature
Substances Involved (all cells):
Gases, small inorganic ions and molecules,
lipid-soluble materials
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Passive process: osmosis
• Movement of water molecules from an area of high
concentration of water to an area of low
concentration of water
• Permeability, concentration gradient, and opposing
pressure affect the rate of movement
• Only water molecules are involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (2 of 6)
© 2015 Pearson Education, Inc.
Water
Osmosis
Example:
If the solute concentration outside
a cell is greater than the inside the
cell, water molecules will move
across the plasmalemma into the
extracellular fluid.
Osmosis is the diffusion of water molecules
(rather than solutes) across a selectively
permeable membrane. Note that water
molecules diffusing toward an area of lower
water concentration are moving toward an area
of higher solute concentration. Because solute
concentrations can easily be determined, they
are used to determine the direction and force
of osmotic water movement.
Factors Affecting Rate:
Size of the solute concentration gradient;
opposing pressure
Substances Involved:
Water only
Solute
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Passive process: facilitated diffusion
• Solutes are passively transported by a carrier
protein
• Concentration gradient, size and charge of the
solute, temperature, and number of carrier proteins
affect the rate of movement
• Glucose and amino acids are involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (3 of 6)
© 2015 Pearson Education, Inc.
Glucose Facilitated diffusion
Example:
Nutrients that are insoluble
in lipids or too large to fit
through membrane
channels may be trans-
ported across the plasma-
lemma by carrier proteins.
Many carrier proteins move
a specific substance in one
direction only, either into or
out of the cell, after first
binding the substance at a
specific receptor site.
In facilitated diffusion, solutes are
passively transported across a
plasmalemma by a carrier protein. As
in simple diffusion, the direction of
movement follows the concentration
gradient.
Factors Affecting Rate:
Magnitude of the concentration
gradient; size, charge, and solubility of
the solutes; temperature; availability
of carrier proteins
Substances Involved (all cells):
Glucose and amino acids
Extracellular
fluid
Receptor
site Carrier
protein
Cytoplasm
Carrier protein releases
glucose into cytoplasm
Plasmalemma
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Active process: active transport
• Solutes are actively transported by a carrier protein
regardless of the concentration gradient
• ATP, number of carrier proteins affect the rate of
movement
• Sodium, potassium, calcium, and magnesium ions
are involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (4 of 6)
© 2015 Pearson Education, Inc.
Extracellular
fluid
Active transport
Example:
One of the most common
examples of active transport
is the sodium–potassium
exchange pump. For each
molecule of ATP consumed,
three sodium ions are
ejected from the cell and two
potassium ions are reclaimed
from the extracellular fluid.
Using active transport, carrier proteins can move
specific substances across the plasmalemma despite an
opposing concentration gradient. Carrier proteins that
move one solute in one direction and another solute in
the opposite direction are called exchange pumps.
Factors Affecting Rate:
Availability of carrier proteins, solutes, and ATP
Substances Involved:
Na+, K+, Ca2+, Mg2+ (all cells); other solutes in special
cases
Sodium–potassium
exchange pump
Cytoplasm
3 Na+
2 K+ ATP ADP
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Active process: endocytosis
• Pinocytosis: vesicles bring small molecules into the
cell
• A variety of stimuli affect the rate of movement (not
fully understood)
• Extracellular fluid is involved
• Phagocytosis: vesicles bring solid particles into the
cell
• Presence of extracellular pathogens affects the rate
of movement
• Bacteria, viruses, foreign matter, and cell debris are
involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (5 of 6)
© 2015 Pearson Education, Inc.
Endocytosis is the packaging of extracellular materials into a vesicle (a membrane-bound sac) for importation into the cell.
Pinocytotic
vesicle
forming
Endocytosis
Example:
Water and small
molecules within a
vesicle may enter
the cytoplasm
through carrier-
mediated transport
or diffusion.
In pinocytosis, vesicles form at the
plasmalemma and bring extracellular fluid
and small molecules into the cell. This
process is often called “cell drinking.”
Cell Pseudopodium
extends to
surround object
Cell
Phagocytic vesicle
Extracellular fluid Target molecules
Receptor
proteins
Cytoplasm
Vesicle
containing
target
molecules
Example:
Large particles are
brought into the cell
when cytoplasmic
extensions (called
pseudopodia) engulf
the particle and form
a phagocytic vesicle.
Example:
Each cell has
specific sensitivities
to extracellular
materials, depend-
ing on the kind of
receptor proteins
present in the
plasmalemma.
In phagocytosis, vesicles form at
the plasmalemma to bring solid
particles into the cell. This process is
often called “cell eating.”
Factors Affecting Rate:
Stimulus and mechanism not under-
stood
Substances Involved:
Extracellular fluid and its associated
solutes
Pinocytosis Phagocytosis Receptor-mediated endocytosis
Factors Affecting Rate:
Presence and abundance of
extracellular pathogens or debris
Substances Involved:
Bacteria, viruses, cell debris, and
other foreign material
In receptor-mediated
endocytosis, target molecules
bind to specific receptor proteins
on the membrane surface,
triggering vesicle formation.
Factors Affecting Rate:
Number of receptors on the
plasmalemma and the concentration of
target molecules (called ligands)
Substances Involved (all cells):
Many examples, including cholesterol and
iron ions
Cellular Anatomy
• Membrane Permeability of the Plasmalemma
• Active process: exocytosis
• The release of intracellular material to the
extracellular area
• Requires ATP and calcium ions for movement
• Fluid and cellular waste and secretory products are
involved
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Figure 2.4 Membrane Permeability: Active and Passive Processes (6 of 6)
© 2015 Pearson Education, Inc.
Cell
Exocytosis
Example:
Cellular wastes that
accumulate in vesicles
are ejected from the cell.
Exocytosis is the release of
fluids and/or solids from cells
when intracellular vesicles fuse
with the plasmalemma.
Material ejected from cell
Factors Affecting Rate:
Stimulus and mechanism incompletely
understood; requires ATP and calcium
ions
Substances Involved (all cells):
Fluid and cellular wastes; secretory
products are released by some cells
Cellular Anatomy
• Extensions of the Plasmalemma: Microvilli
• Fingerlike projections of the plasmalemma
• Absorb material from the ECF
• Increase the surface area of the plasmalemma
• Microvilli can bend back and forth in a waving
manner
• This movement helps to circulate extracellular fluid
• This movement helps absorb nutrients
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Figure 2.1 Anatomy of a Typical Cell
© 2015 Pearson Education, Inc.
Microvilli
Secretory vesicles
Cytosol
Lysosome
Centrosome
Centriole
Chromatin
Nucleoplasm
Nucleolus
Nuclear envelope surrounding nucleus
Cytoskeleton
Plasmalemma Free ribosomes
Fixed ribosomes
Rough endoplasmic reticulum
Smooth endoplasmic reticulum
Nuclear pores
Peroxisome
Mitochondrion
Golgi apparatus
Cellular Anatomy
• The Cytoplasm
• Term for all of the intracellular material
• Cytosol
• Consists of the ICF (intracellular fluid)
• Consists of nutrients, protein, and waste products
• Organelles
• These are intracellular structures that perform
specific functions
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Figure 2.1 Anatomy of a Typical Cell
© 2015 Pearson Education, Inc.
Microvilli
Secretory vesicles
Cytosol
Lysosome
Centrosome
Centriole
Chromatin
Nucleoplasm
Nucleolus
Nuclear envelope surrounding nucleus
Cytoskeleton
Plasmalemma Free ribosomes
Fixed ribosomes
Rough endoplasmic reticulum
Smooth endoplasmic reticulum
Nuclear pores
Peroxisome
Mitochondrion
Golgi apparatus
Cellular Anatomy
• The Cytoplasm
• Cytosol
• Contains a higher concentration of potassium ions
and a lower concentration of sodium ions as
compared to the ECF
• Consists of a net negative charge
• Contains a high concentration of protein
• Contains a small quantity of carbohydrates
• Contains a large reserve of amino acids and lipids
• Contains large amounts of inclusions
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Cellular Anatomy
• The Cytoplasm
• Organelles
• Nonmembranous organelles
• Cytoskeleton Centrioles Cilia
Flagella Ribosomes
• Membranous organelles
• Mitochondria Nucleus Endoplasmic
reticulum
Golgi apparatus Lysosomes Peroxisomes
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Cellular Anatomy
• Nonmembranous Organelles (details)
• The cytoskeleton consists of:
• Microfilaments
• Intermediate filaments
• Thick filaments
• Microtubules
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Cellular Anatomy
• Nonmembranous Organelles (details)
• Microfilaments: consist of actin protein
• Anchor cytoskeleton to integral proteins
• Stabilize the position of membrane proteins
• Anchor plasmalemma to the cytoplasm
• Produce movement of the cell or a change in the
cell’s shape
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Cellular Anatomy
• Nonmembranous Organelles (details)
• Intermediate filaments
• Provide strength
• Stabilize organelle position
• Transport material within the cytosol
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Cellular Anatomy
• Nonmembranous Organelles (details)
• Thick filaments: composed of myosin protein
• Found in muscle cells: involved in muscle
contraction
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Cellular Anatomy
• Nonmembranous Organelles (details)
• Microtubules: composed of tubulin protein
• Involved in the formation of centrioles
• perform a function during cell reproduction
• Involved in moving duplicated chromosomes to
opposite poles of the cell
• perform a function during cell reproduction
• Involved in anchoring organelles
• Involved in moving cell organelles
• Involved in moving the entire cell
• Involved in moving material across the surface of
the cell
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Figure 2.5 The Cytoskeleton
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Microvilli
a
b
Microfilaments
Plasmalemma
Terminal web
Mitochondrion
Intermediate
filaments
Endoplasmic
reticulum
Microtubule
Secretory
vesicle
SEM × 30,000
LM × 3200
c
The cytoskeleton provides
strength and structural
support for the cell and its
organelles. Interactions
between cytoskeletal elements
are also important in moving
organelles and in changing
the shape of the cell.
A SEM image of the
microfilaments and microvilli
of an intestinal cell.
Microtubules in a living
cell, as seen after
fluorescent labeling.
Cellular Anatomy
• Nonmembranous Organelles (details)
• Examples of microtubules
• Centrioles
• Cilia
• Flagella
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Table 2.2 A Comparison of Centrioles, Cilia, and Flagella
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Figure 2.6 Centrioles and Cilia
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Microtubules
Microtubules
Plasmalemma
Basal body
Power stroke Return stroke
a A centriole consists of nine microtubule triplets (9 + 0 array). The centrosome contains a pair of centrioles oriented at right angles to one another.
b
c
A cilium contains nine pairs of microtubules surrounding a central pair (9 + 2 array).
TEM × 240,000 A single cilium swings forward and then returns to its original position. During the power stroke, the cilium is relatively stiff, but during the return stroke, it bends and moves parallel to the cell surface.
Cellular Anatomy
• Nonmembranous Organelles (details)
• Ribosomes
• Free ribosomes: float in the cytoplasm
• Fixed ribosomes: attached to the endoplasmic
reticulum
• Both are involved in producing protein
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Figure 2.1 Anatomy of a Typical Cell
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Microvilli
Secretory vesicles
Cytosol
Lysosome
Centrosome
Centriole
Chromatin
Nucleoplasm
Nucleolus
Nuclear envelope surrounding nucleus
Cytoskeleton
Plasmalemma Free ribosomes
Fixed ribosomes
Rough endoplasmic reticulum
Smooth endoplasmic reticulum
Nuclear pores
Peroxisome
Mitochondrion
Golgi apparatus
Figure 2.6 Centrioles and Cilia
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Microtubules
Microtubules
Plasmalemma
Basal body
Power stroke Return stroke
a A centriole consists of nine microtubule triplets (9 + 0 array). The centrosome contains a pair of centrioles oriented at right angles to one another.
b
c
A cilium contains nine pairs of microtubules surrounding a central pair (9 + 2 array).
TEM × 240,000 A single cilium swings forward and then returns to its original position. During the power stroke, the cilium is relatively stiff, but during the return stroke, it bends and moves parallel to the cell surface.
Cellular Anatomy
• Membranous Organelles (details)
• Double-membraned organelles
• Mitochondria: produce ATP
• Nucleus: contains chromosomes
• Endoplasmic reticulum: network of hollow tubes
• Golgi apparatus: modifies protein
• Lysosomes: contain cellular digestive enzymes
• Peroxisomes: contain catalase to break down
hydrogen peroxide
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Cellular Anatomy
• Membranous Organelles (details)
• Mitochondria
• Consist of cristae
• Consist of mitochondrial matrix
• Produce ATP
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Figure 2.8 Mitochondria
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Inner membrane
Organic molecules and O2
CO2
ATP
Matrix Cristae
Outer membrane
Enzymes
Cytoplasm of cell Cristae Matrix
TEM × 61,776
Cellular Anatomy
• Membranous Organelles (details)
• Nucleus: control center of the cell
• Nucleoplasm
• Nuclear envelope
• Perinuclear space
• Nuclear pores
• Nuclear matrix
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Figure 2.9ab The Nucleus
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Perinuclear
space
a
TEM × 4828
Nucleoplasm
Chromatin
Nucleolus
Nuclear envelope
Nuclear pores
TEM showing important nuclear structures.
Nuclear
envelope
Perinuclear
space
Nuclear
pore
A nuclear pore and the
perinuclear space.
b
Figure 2.9c The Nucleus
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SEM × 9240
Inner membrane of
nuclear envelope
Broken edge of
outer membrane
Outer membrane of
nuclear envelope
The cell seen in this SEM was frozen and then broken apart so that internal structures could be seen. This technique, called freeze-fracture, provides a unique perspective on the internal organization of cells. The nuclear envelope and nuclear pores are visible; the fracturing process broke away part of the outer membrane of the nuclear envelope, and the cut edge of the nucleus can be seen.
c
Cellular Anatomy
• Membranous Organelles: Nucleus
• Chromosomes:
• DNA wrapped around proteins called histones
• Nucleosomes
• Chromatin
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Figure 2.10 Chromosome Structure
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Nucleus of nondividing cell
a
Chromatin in nucleus Loosely coiled
nucleosomes,
forming chromatin.
Sister chromatids
Centromere
Kinetochore
Dividing cell
Visible chromosome
Supercoiled
region
In cells that are not dividing, the DNA is loosely coiled,
forming a tangled network known as chromatin.
b When the coiling becomes tighter, as it does in preparation for cell division, the DNA
becomes visible as distinct structures called chromosomes. Chromosomes are composed
of two sister chromatids which attach at a single point, the centromere. Kinetochores are
the region of the centromere where spindle fibers attach during mitosis.
DNA double
helix
Histones
Nucleosome
Cellular Anatomy
• Membranous Organelles (details)
• Endoplasmic reticulum (ER)
• There are two types
• Rough endoplasmic reticulum (RER)
• Smooth endoplasmic reticulum (SER)
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Cellular Anatomy
• Membranous Organelles (details)
• Rough endoplasmic reticulum
• Consists of fixed ribosomes
• Proteins enter the ER
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Figure 2.11 The Endoplasmic Reticulum
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Ribosomes
Cisternae
Rough endoplasmic
reticulum with fixed
(attached) ribosomes
Free
ribosomes
Smooth
endoplasmic
reticulum
Endoplasmic
Reticulum
TEM × 11,000
Figure 2.7 Ribosomes
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Nucleus
a
Free
ribosomes
Endoplasmic
reticulum with
attached fixed
ribosomes
Small ribosomal
subunit
Large ribosomal
subunit
TEM × 73,600
Both free and fixed ribosomes can
be seen in the cytoplasm of this cell.
An individual
ribosome,
consisting of small
and large subunits.
b
Cellular Anatomy
• Membranous Organelles (details)
• Smooth endoplasmic reticulum
• Synthesizes lipids, steroids, and carbohydrates
• Storage of calcium ions
• Detoxification of toxins
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Cellular Anatomy
• Membranous Organelles (details)
• Golgi apparatus
• Synthesis and packaging of secretions
• Packaging of enzymes (modifies protein)
• Renewal and modification of the plasmalemma
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Figure 2.12 TEM of the Golgi Apparatus
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Vesicles
Maturing
(trans) face
Forming
(cis) face
Golgi apparatus TEM × 83,520
Cellular Anatomy
• Membranous Organelles (details)
• Lysosomes
• Fuse with phagosomes to digest solid materials
• Recycle damaged organelles
• Sometimes rupture, thus killing the entire cell
(called autolysis)
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Cellular Anatomy
• Membranous Organelles (details)
• Peroxisomes
• Consist of catalase
• Abundant in liver cells
• Convert hydrogen peroxide to water and oxidants
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Cellular Anatomy
• Membrane Flow
• This is the continuous movement and recycling of
the cell membrane
• Transport vesicles connect the endoplasmic
reticulum with the Golgi apparatus
• Secretory vesicles connect the Golgi apparatus
with the plasmalemma
• Vesicles remove and recycle segments of the
plasmalemma
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Figure 2.13 Functions of the Golgi Apparatus (1 of 3)
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Cytoplasm
Transport vesicle
Rough ER
mRNA Ribosome Endoplasmic Reticulum
Golgi Apparatus Synthesis and
Packaging of
Secretions: Steps
2 Secretory products are
packaged into transport
vesicles that eventually
bud off from the ER.
These transport vesicles
then fuse to create the
forming (cis) face of the
Golgi apparatus.
Protein and glycoprotein
synthesis occurs in the
rough endoplasmic
reticulum (RER). Some
of these proteins and
glycoproteins remain
within the ER.
Cisterna Forming (cis) face
1
Figure 2.13 Functions of the Golgi Apparatus (2 of 3)
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Secretory vesicle
TEM × 75,000
The maturing (trans) face
generates vesicles that
carry materials away
from the Golgi apparatus.
Secretory material
Plasmalemma
Secretory vesicle
Plasmalemma
Exocytosis at the
surface of a cell
Cytoplasm
Lysosome
Cytoplasm
Maturing (trans) face
Forming (cis) face
Cisterna
Golgi Apparatus
Packaging of Enzymes for Use
in the Cytosol
Renewal or Modification of
the Plasmalemma
Synthesis and Packaging
of Secretions
Synthesis and
Packaging of
Secretions: Steps
4
Each cisterna physically
moves from the forming
face to the maturing
face, carrying with it its
associated proteins.
This process is called cisternal progression.
3
Intercellular Attachment
• Many cells form permanent or temporary
attachment to other cells
• Attach via cell adhesion molecules (CAMs)
• Attach via cellular cement (proteoglycans)
• Examples of Intercellular Attachment
• Communicating junctions
• Adhering junctions
• Tight junctions
• Anchoring junctions
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Intercellular Attachment
• Communicating Junctions
• Also called gap junctions
• Two cells held together via protein called
connexon
• This protein is a type of channel protein
• Attach via cell adhesion molecules (CAMs)
• Attach via cellular cement (proteoglycans)
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Figure 2.14ab Cell Attachments
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Embedded
proteins
(connexons)
a
Hemidesmosome
Tight junction
Terminal web
Button
desmosome
Communicating junction b Communicating
junctions permit
the free diffusion
of ions and small
molecules
between two cells. A diagrammatic view of an
epithelial cell showing the major
types of intercellular connections.
Zonula adherens
Intercellular Attachment
• Adhering Junctions
• Tight junctions, also called occluding junctions
• Prevent the movement of water and other
molecules from passing between the cells
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Intercellular Attachment
• Anchoring Junctions
• Zona adherens (adhesion belt) is a sheetlike
anchoring material
• Provides strong links that cells can shed from the
body in sheets (ex. dandruff)
• Macula adherens (desmosome) is a small,
localized anchoring junction
• Most abundant in superficial layers of the skin
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Figure 2.14ac Cell Attachments
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Hemidesmosome
Tight junction
Terminal web
Button
desmosome
Communicating junction
Zonula adherens
Tight junction
Zonula
adherens
Interlocking
junctional
proteins
a A diagrammatic view of an
epithelial cell showing the major
types of intercellular connections.
c A tight junction is formed by the
fusion of the outer layers of two
plasmalemmae. Tight junctions
prevent the diffusion of fluids
and solutes between the cells.
Figure 2.14ad Cell Attachments
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a
Hemidesmosome
Tight junction
Terminal web
Button
desmosome
Communicating junction
A diagrammatic view of an
epithelial cell showing the major
types of intercellular connections.
Zonula adherens
Intermediate filaments (cytokeratin)
Cell adhesion
molecules
(CAMs)
Dense area
Intercellular cement
d Anchoring junctions
attach one cell to another.
A macula adherens has a
more organized network
of intermediate filaments.
An adhesion belt is a form
of anchoring junction that
encircles the cell. This
complex is tied to the
microfilaments of the
terminal web.
Intercellular Attachment
• Anchoring junctions
• Focal adhesions (focal contacts)
• Connect intracellular microfilaments to protein
fibers
• Found in epithelial tissue that migrates during
wound repair
• Hemidesmosomes
• Found in connecting cells that are exposed to a lot
of abrasion
• Examples are the cornea of the eye, skin, vaginal
tissue, oral cavity, and esophagus
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a
Hemidesmosome
Tight junction
Terminal web
Button
desmosome
Communicating junction
A diagrammatic view of an
epithelial cell showing the major
types of intercellular connections.
Zonula adherens
Clear layer
Dense layer
Basal lamina
e Hemidesmosomes attach an epithelial
cell to extracellular structures, such as
the protein fibers in the basal lamina.
Figure 2.14ae Cell Attachments
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The Cell Life Cycle
• Cell reproduction consists of special events
• Interphase
• Mitosis
• Prophase
• Metaphase
• Anaphase
• Telophase
• Cytokinesis
• Overlaps with anaphase and telophase
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The Cell Life Cycle
• Cell Reproduction (Interphase)
• Everything inside the cell is duplicating
• Consists of G1, S, and G2 phases
• G1: duplication of organelles and protein synthesis
• S: Chromosome replication and DNA synthesis and
histone synthesis
• G2: protein synthesis
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Figure 2.16 DNA Replication
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KEY
Adenine
Guanine
Cytosine
Thymine
Segment 2
DNA polymerase
DNA nucleotide
Segment 1
DNA
polymerase
The Cell Life Cycle
• Cell Reproduction (Mitosis)
• Prophase
• The first phase of mitosis
• Metaphase
• Paired chromatids line up in the middle of the
nuclear region
• Anaphase
• Paired chromatids separate to opposite poles of
the cell
• Telophase
• Two new nuclear membranes begin to form
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Figure 2.17 Mitosis
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Nucleus
Nuclear
membrane
Spindle
fibers
Centrioles
(two pairs)
Astral
rays
Chromosomal
microtubules
Centromere
Chromosome
with two sister
chromatids
Interphase Prophase
Early prophase
Metaphase
Late prophase
Anaphase Telophase Cytokinesis
Chromosomal
microtubules
Metaphase
plate
Daughter
chromosomes
Cleavage
furrow
Daughter
cells
The Cell Life Cycle
• Cell Reproduction (Cytokinesis)
• Cell membrane begins to invaginate, thus forming
two new cells
• Many times this phase actually begins during
anaphase
• This is the conclusion of cell reproduction
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Figure 2.15 The Cell Life Cycle
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THE
CELL
CYCLE
INTERPHASE
S
DNA
replication,
synthesis
of
histones G2
Protein
synthesis
G1
Normal
cell functions
plus cell growth,
duplication of
organelles,
protein
synthesis
Indefinite period
G0
Specialized
cell functions
M
MITOSIS AND
CYTOKINESIS
(See Figure 2.17)