Chapter 3
The cellular level of
organisation
Introduction
The purpose of the chapter is to:
• Introduce the parts of a cell
• Discuss the importance of the plasma membrane
• Discuss the components of the cytoplasm
• Compare and contrast mitosis and meiosis
• Understand the effects ageing has on the cell
Parts of a cell
• The cell can be subdivided into 3 parts:
1. Plasma (cell) membrane
2. Cytoplasm
• Cytosol
• Organelles
3. Nucleus
• Chromosomes
• Genes
Parts of a cell
Figure 3.1
The plasma membrane
• The plasma membrane is a flexible yet sturdy barrier
that surrounds and contains the cytoplasm of the cell
Figure 3.2
Membrane proteins
• Two types of membrane proteins are
– Integral (also called transmembrane) proteins
– Peripheral proteins
Functions of membrane proteins
– Membrane proteins
can serve a variety of
functions
– The different proteins
help determine many
of the functions of
the cell membrane
Figure 3.3
Membrane fluidity
• Membranes are fluid structures because most of the
membrane lipids and many of the membrane
proteins move easily in the bilayer
– Membrane lipids and proteins are mobile in their
own half of the bilayer
• Cholesterol serves to stabilise the membrane and
reduce membrane fluidity
Membrane permeability
• Plasma membranes are selectively permeable
– The lipid bilayer is always permeable to small,
nonpolar, uncharged molecules
– Transmembrane proteins that act as channels or
transporters increase the permeability of the
membrane
– Macromolecules are only able to pass through the
plasma membrane by vesicular transport
Gradients across the plasma membrane
• A concentration gradient is the difference in the
concentration of a chemical between one side of the
plasma membrane and the other
• An electrical gradient is the difference in
concentration of ions between one side of the
plasma membrane and the other
• Together, these gradients make up an
electrochemical gradient
Transport across the plasma membrane
• Transport processes that move substances across the
cell membrane are:
– Passive processes
• Simple diffusion
• Facilitated diffusion
• Osmosis
– Active processes
• Active transport
• Vesicular transport
Passive processes: Simple diffusion
• Diffusion is influenced by:
• Steepness of the concentration gradient
• Temperature
• Mass of diffusion substance
• Surface area
• Diffusion distance
Figure 3.4
Facilitated diffusion
• Transmembrane proteins help solutes that are too
polar or too highly charged move through the lipid
bilayer
• The processes involved are:
– Channel-mediated facilitated diffusion
– Carrier-mediated facilitated diffusion
Channel-mediated facilitated diffusion
Figure 3.6
Carrier-mediated facilitated diffusion
Figure 3.7
Diffusion: A comparison
Figure 3.5
Osmosis
• The net movement of a solvent through a
selectively permeable membrane from an area of
high concentration to an area of low
concentration
Figure 3.8
Tonicity
• Tonicity of a solution relates to how the solution
influences the shape of body cells
Figure 3.9
Active processes: Primary active
transport
• Energy derived from ATP changes the shape of a
transporter protein which pumps a substance across
a plasma membrane against its concentration
gradient
Figure 3.10
Secondary active transport
• Energy stored (in a hydrogen or sodium
concentration gradient) is used to drive other
substances against their own concentration gradients
Figure 3.11
Active transport in vesicles: Receptor
-mediated endocytosis
Figure 3.12
Active transport in vesicles:
Phagocytosis
Figure 3.13
Active transport in vesicles: Bulk phase
endocytosis (Pinocytosis)
Figure 3.14
Active transport in vesicles: Exocytosis &
transcytosis
• Exocytosis – membrane-enclosed secretory vesicles
fuse with the plasma membrane and release their
contents into the extracellular fluid
• Transcytosis – a combination of endocytosis and
exocytosis used to move substances from one side of
a cell, across it, and out the other side
A comparison of transport types
A comparison of transport types
Cytoplasm
• Cytosol is also known as the intracellular fluid portion
of the cytoplasm
• Organelles are the specialised structures that have
specific shapes and perform specific functions
Cytoskeleton
Figure 3.15
Centrosome/Centrioles
Figure 3.16
Cilia and flagella
Figure 3.17
Ribosomes
Figure 3.18
Endoplasmic reticulum
Figure 3.19
Golgi complex
Figure 3.20
Figure 3.21
Lysosomes
Figure 3.22
Peroxisomes
• Peroxisomes are structures that are similar in shape
to lysosomes, but are smaller and contain enzymes
that use oxygen to oxidise (break down) organic
substances
Proteasomes
• Proteasomes are barrel-shaped structures that
destroy unneeded, damaged, or faulty proteins by
cutting long proteins into smaller peptides
Copyright © 2014 John Wiley & Sons, Inc. All rights reserved.
Mitochondria
Figure 3.23
Nucleus
Figure 3.24
Nucleus
• The nucleus contains the cell’s hereditary units,
called genes, which are arranged in chromosomes
Figure 3.25
Gene expression
Figure 3.26
Protein synthesis: Transcription
• Transcription occurs
in the nucleus and is
the process by which
genetic information
encoded in DNA is
copied onto a strand
of RNA to direct
protein synthesis
Figure 3.27
Protein synthesis: Translation
• Translation occurs in the nucleus and is the process
of reading the mRNA nucleotide sequence to
determine the amino acid sequence of the newly
formed protein
Figure 3.28
Protein synthesis during transcription
Figure 3.29
Cell division
• Cell division is a process by which cells reproduce
themselves
– Cell cycle
Figure 3.30
Interphase
• G1 phase
• S
• G2 phase Figure 3.31
Mitotic phase: Prophase
• During prophase chromatin condenses into
chromosomes
Figure 3.30
Mitotic phase: Metaphase
• During metaphase centromeres of chromosomes line
up at the metaphase plate
Figure 3.30
Mitotic phase: Anaphase
• During anaphase centromeres of chromosomes split
and sister chromatids move toward opposite poles of
the cell
Figure 3.30
Mitotic phase: Telophase
• During telophase the mitotic spindle dissolves,
chromosomes regain their chromatin appearance,
and a new nuclear membrane forms
Figure 3.30
Cytokinesis
• During cytokinesis a
cleavage furrow
forms and eventually
the cytoplasm of the
parent cell fully splits
– When this is
complete, interphase
begins
Figure 3.30
Control of cell destiny
• 3 possible destinies:
1. Remain alive and functioning without dividing
2. Grow and divide
3. Die
Reproductive cell division: Meiosis I
Figure 3.33
Reproductive cell division: Meiosis II
Figure 3.33 cont.
Cellular diversity
Figure 3.35
Ageing and cells
• As we age:
– Our cells gradually deteriorate in their ability
function normally and in their ability to respond to
environmental stresses
– The numbers of our body cells decreases
– We lose the integrity of the extracellular
components of our tissues