3-3
Cell Shapes and Sizes
•About 200 types of cells in the human body
•Squamous—thin and flat with nucleus creating bulge
•Polygonal—irregularly angular shapes with four or more
sides
•Stellate—starlike shape
•Cuboidal—squarish and about as tall as is wide
•Columnar—taller than wide
•Spheroid to ovoid—round to oval
•Discoid—disc-shaped
•Fusiform—thick in middle, tapered toward the ends
•Fibrous—threadlike shape
•Note: Some of these cell shapes appear as in tissue
sections, but not their three-dimensional shape
Basic Components of a Cell
•Plasma membrane or cell membrane
–Surrounds cell, defines boundaries
–Made of proteins and lipids
–Composition and function can vary from one
region of the cell to another
•Cytoplasm or cytosol
–Organelles
–Cytoskeleton
–Cytosol (intracellular fluid, ICF)
•Extracellular fluid (ECF)
–Fluid outside of cell
3-9
The Glycocalyx
(Glycolipids & Glycoproteins)
of Cell Membrane
•Unique fuzzy coat external to the plasma membrane
–Carbohydrate moieties of membrane glycoproteins and glycolipids
–Unique in everyone but identical twins
•Functions
–Protection – Cell adhesion
–Immunity to infection – Fertilization
–Defense against cancer – Embryonic development
–Transplant compatibility
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Membrane Channel Proteins
•Transmembrane proteins with pores that
allow water and dissolved ions to pass through
membrane
–Some are constantly open
–Some are gated channels that open and close in
response to stimuli
•Ligand (chemically)-regulated gates
•Voltage-regulated gates
•Mechanically regulated gates (stretch and pressure)
•Play an important role in the timing of nerve
signals and muscle contraction
Plasma membrane
EXTRACELLULAR FLUID
CYTOPLASM
Lipid-soluble molecules diffuse
through the plasma membrane
Channel
protein
Small water-soluble
molecules and ions
diffuse through
membrane channels
Large molecules that cannot
diffuse through lipids cannot
cross the plasma membrane
unless they are transported
by a carrier mechanism
Figure 3-15 Diffusion across the Plasma Membrane
3-14
Membrane Transport
•Plasma membrane—a barrier and a gateway between the
cytoplasm and ECF
–Selectively permeable—allows some things through, and prevents
other things from entering and leaving the cell
•Passive transport mechanisms require no ATP
–Random molecular motion of particles provides the necessary energy
–Filtration, diffusion, osmosis
•Active transport mechanisms consumes ATP
–Active transport and vesicular transport
•Carrier-mediated mechanisms use a membrane protein to
transport substances from one side of the membrane to the
other
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Osmolarity and Tonicity
•Hypotonic solution
–Has a lower concentration of nonpermeating solutes than
intracellular fluid (ICF)
•High water concentration
–Cells absorb water, swell, and may burst (lyse)
•Hypertonic solution
–Has a higher concentration of nonpermeating solutes
•Low water concentration
–Cells lose water + shrivel (crenate)
•Isotonic solution
–Concentrations in cell and ICF are the same
–Cause no changes in cell volume or cell shape
–Normal saline
Solute
molecules
Water
molecules
In an isotonic saline solution, no osmotic flow occurs, and
these red blood cells appear normal as biconcave disc shape.
SEM of normal RBC
in an isotonic solution
Figure 3-17a Osmotic Flow across a Plasma Membrane
SEM of RBC in a
hypotonic solution
Immersion in a hypotonic saline solution results
in the osmotic flow of water into the cells. The
swelling may continue until the plasma membrane
ruptures or lyses by “hemolysis”.
Figure 3-17b Osmotic Flow across a Plasma Membrane
SEM of crenated RBCs
in a hypertonic solution
Exposure to a hypertonic solution results in the movement
of water out of the cell. The red blood cells shrivel and
become crenated.
Figure 3-17c Osmotic Flow across a Plasma Membrane
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The Nucleus
•Nucleus—largest organelle (5 m in diameter)
–Most cells have one nucleus
–A few cells are anuclear or multinucleate
•Nuclear envelope—two unit membranes surround
nucleus
–Perforated by nuclear pores formed by rings of protein
•Regulate molecular traffic through envelope
•Hold two unit membranes together
•Nucleoplasm—cytoplasm of nucleus
–Chromatin (threadlike matter) composed of DNA and
protein
–Nucleoli—one or more dark masses where ribosomes
are produced
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Ribosomes
•Ribosomes—small circular granules that make
protein and RNA
–Found in nucleoli, cytosol, and surface of rough ER,
and nuclear envelope
•They “read” coded genetic messages
(messenger RNA) and assemble amino acids
into proteins
Golgi apparatus
Stacks of flattened
membranes (cisternae)
Functions:
Storage and packaging
of products and lysozyme
enzymes as vesicles
Mitochondria
Double membranes where
Inner membrane (cristae)
contains important enzymes
for metabolism
Function:
Produce ATP energy
Endoplasmic reticulum (ER)
Network of
membranous
channels
Functions:
Synthesis, storage,
and transport of
products
Rough ER
packages
newly made
proteins
Smooth ER
synthesizes
lipids and
carbohydrates
Peroxisomes
Vesicles that contain
enzymes
Functions:
Catabolism of organic
compounds and neutralization
of toxic compounds
NUCLEUS
Plasma membrane
Nonmembranous organelles
Membranous organelles
Figure 3-1 Anatomy of a Cell (Part 5 of 8)
3-28
•Endoplasmic reticulum—interconnected channels
called cisternae enclosed by unit membrane
•Rough endoplasmic reticulum—composed of
parallel, flattened sacs covered with ribosomes
–Produces proteins of the plasma membrane
–Synthesizes proteins that are packaged in other
organelles or secreted from cell
•Smooth endoplasmic reticulum
–Lack ribosomes so no protein synthesis
–Synthesizes steroids and lipids instead
–Manufactures lipid membranes of the cell
Endoplasmic Reticulum
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Golgi Complex
•Golgi complex—a small system of cisternae that
synthesize carbohydrates and put the finishing
touches on protein and glycoprotein synthesis
–Receives newly synthesized proteins from rough ER
–Sorts them, cuts and splices some of them, adds
carbohydrate moieties to some, and packages the
protein into membrane-bound Golgi vesicles
•Some become lysosomes
•Some migrate to plasma membrane and fuse to it
•Some become secretory vesicles for later release
Golgi
apparatus
Autolysis
liberates
digestive
enzymes
Primary
lysosome
Reabsorption
Endosome
Damaged
organelle
Secondary
lysosome
Reabsorption
Secondary
lysosome
Endocytosis
Extracellular
solid or fluid
Exocytosis
ejects residue
Exocytosis
ejects residue
The lysosomal membrane
breaks down during autolysis
following injury to or death
of the cell.
A primary lysosome fuses
with an endosome containing
fluid or solid materials from
outside the cell.
A primary lysosome fuses
with the membrane of
another organelle like the
mitochondrion.
Activation of lysosomes
occurs when:
Figure 3-8 Lysosome Functions
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Lysosomes & Peroxisomes
•Lysosomes—vesicles that contain digestive
enzymes to digest food or kill pathogens (bacteria
and viruses)
–Autophagy—digest and dispose of worn out
mitochondria and other organelles
–Autolysis—“cell suicide”: some cells are meant to do a
certain job and then destroy themselves
•Peroxisomes—resemble lysosomes but contain
enzymes to detoxify or neutralize poisons
- Abundant in liver and kidney
CYTOPLASM
MATRIX
Pyruvate
Glycolysis
Glucose
Citric Acid
Cycle
ADP
phosphate
Enzymes
and
coenzymes
of cristae
MITOCHONDRION
This is an overview of the role of mitochondria in energy
production. Mitochondria absorb short carbon chains (such as
pyruvate) and oxygen and generate carbon dioxide and ATP.
Figure 3-9b Mitochondria