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CELL INTRODUCTION
Cell
Theory
P R I N C I P L E S O F T H E C E L L T H E O R Y
Cells only
3. arise from pre existing
-
C A V E A T S T O T H E C E L L T H E O R Y
Certain
types of cells Itissues do not conform to a standard notion of what constitutes a cell 8
e.
STRIATED MUSCLE FIBRES :
muscle cells fuse to form fibres that
may be very long 17300mm)
-
e.
A SEPTATE FUNGAL HYPHAE :
FUNGI
may have filamentous structures called hyphae
-
some
fungi are not partitioned by septa hence have a -
continuous cytoplasm along the
length of the hyphae Septa
* idea that
challenges the living structures are composed of DISCRETE CELLS
GIANTcertain
ALGAE :
a.
very LARGE
to
species of unicellular algae may grow sizes
↳ E. 68 acetabulation exceed 7cm
may
in
length
*
challenges idea that
the
larger organisms are always made of
many microscopic cells
Functions of life
UNICELLULAR ORGANISMS -
the smallest
organisms capable of independent life
composed of single cell
-
a
↳ must be able to
All living things carry out 7 basic functions integral to survival 8
carry out all the
life functions
METABOLISM undertake essential chemical reactions
living things
e. -
REPRODUCTION
living things produce offspring
*o
either sexually asexually
-
,
or
I
SENSITIVITY
living things responsive to internal and external
o.•
stimuli
-
are
HOMEOSTASIS
living things
*o
maintain stable , internal environment
-
EXCRETION
living things exhibit the removal
o.O
waste products
-
of
a. NUTRITION -
GROWTH
living things change shape
a.
and size
-
can move or
mnemonic → MR. SHENG
1. PARAMECIUM (heterotroph)
e.
a.
solid wastes are removed iaap ,
white liquid
wastes are
pumped out viaaaoue (
excretion)
essential gases enter leg G) and exit leg CO2) the cell viadiffus.to ( homeostasis)
e.
paramecia divide
asexually (fission) although horizontal
gene transfer conjugation
e.
can occur via
(reproduction)
2. SCENE DESMUS (autotroph)
scene desmus
exchange gases and other essential materials via
a.
photosynthesis (metabolism)
daughter cells the internal
a.
motile auto via
form as non
spores
-
may as
form
SA Vol Ratio
*
Cells need to produce chemical
energy (via metabolism) to survive and this requires the exchange of
materials with the environment
a.
the rate of metabolism of a cell is a
function of its mass / volume ( larger cells need
a.
the rate of material exchange is a function of its surface area (large membrane surface
*
(units) leading
'
As a cell
grows ,
volume ( units ) increases faster than surface area ,
to a decreased
SA Vol ratio
:
if metabolic rate exceeds the rate of vital materials and wastes flow Vol
a.
exchange of SA :
)
ratio the cell will eventually die
,
hence
a.
Vol ratio
growing cells tend to divide and remain small in order to maintain a
high SA :
I N C R E A S I N G S A i V O L R A T I 0
Cells and tissues that are specialized for gas or material exchanges
will increase their surface area to optimise material transfer
intestinal tissue
of the digestive tract may form
a.
a ruffled structure
WILL 1) to increase surface area
e.
alveoli within the lungs have membranous extensions called micro villi ,
magnification
C A L C U L A T I O N O F M A G N I F I C A T I O N
e.
To calculate the linear magnification drawing the should be used :
of a or
image , following equation
C A L C U L A T I O N O F A C T U A L 5 I 2 E
actual size =
image size (w/ ruler)
magnifications
Light microscopes use visible
light and a combination of lenses to magnify images of mounted specimens
•
TITLE to the specimen (e.g : cell)
identify organism tissue
-
name of ,
or
°
MAGNIFICATION ISCALE -
°
identifiable structures should be clearly labelled (drawings only reflect what is seen , NOT idealised )
versions
5 U M M A R Y O F V I 5 1 13 L E C E L L F E A T U R E S
U N D E R L 1 G H T M 1 C R O S C O P Y
Emergent Properties
\
"
The whole
"
than the
is
greater sum
of its parts
-
ARISTOTLE
e.
MULTICELLULAR ORGANISMS are capable of completing functions that unicellular organisms could NOT
undertake
In multicellular organisms :
e.
cells be grouped together to form tissues
may
then tissues
a.
organ
0 R 6 A N I S A T I O N O F M U L T 1 C E L L U L A R
O R G A N I S M S
Cell Differentiation
DIFFERENTIATION -
the process during development whereby newly formed cells become mciad and
distinct from one another as
they mature
•
The activation of different instructions (genes) within a
given cell
by chemical
signals will cause it
to differentiate
C E L L S P E C 1 A L I 5 A T I O N V 1 A
D I F F E R E N T 1 A L G E N E E X P R E S S I O N
G E N E P A C K A G I N G
a.
inactive genes are
typically packaged in a more condensed form called HETEROCHROMATIN ( saves
space ,
not transcribed )
Differentiated cells will have different regions of DNA packaged as EUCHROMATIN and HETEROCHROMATIN
E U C H R O M A T I N V S H E T E R O C H R O M A T I N
Stem cells
stem cells are un specialised cells that have TWO KEY QUALITIES 8
e.
I. SELF RENEWAL -
can
continuously divide and replicate
types
-
T Y P E S O F S T E M C E L L s
)o•
(e.g zygote
:
ANYcelltype-le.gr embryonic
PLURIPOTENT can form stem cells)
-
e.
can
UNI POTENT not differentiate BUT are capable of self renewal leg progenitor cells
e.
can
-
:
, ,
U S E S O F S T E M C E L L S
as source
ALLothercelttypesmaybederived-NON.SI
EM CELL -
cell types that are not capable of self renewal (e.g : a mitotic nerve tissues )
As these tissues CANNOT be stem cells have become viable therapeutic
regenerated or replaced ,
a
o•
E X A M P L E S O F S T E M C E L L T H E R A P Y
①s t a r
g a r d t 's D i s e a s e
caused
by mutation that
impairs energy transport
e.
in
genea
②
'
P a r k i n s o n s D i s e a s e
↳ a
degenerative disorder of the central nervous
system ( CN5) caused by the death of dopamine
-
e.
DOPAMINE -
{I rspifgigwdigtfagq.no#abnfiofyement
,
tremors
a.
individuals w/ PARKINSON 'S DISEASE . . .
③ OTHER
therapeutic examples
e.
LEUKEMIA :
bone marrow transplants for cancer patients who are immunocom prised as a
result of chemotherapy
PARAPLEGIA by spinal injuries to paralysed victims to
damage
:
enable
repair caused regain
a.
movement
type 1 diabetics
graft new
E G O F T H E R A P E U T 1 C S T E M C E L L U S E
e.
EMBRYOS (may be specially created by therapeutic cloning)
e.
UMBILICAL CORD BLOOD or PLACENTA of a newborn baby
ETHICAL CONSIDERATIONS associated w/ the therapeutic use of stem cells will DEPEND ON THE SOURCE
application
stem cells derived from umbilical cord blood need to be stored and preserved at
a.
cost , raising issues of
availability and access
greatest yield pluripotent stem cells
e.
Stem cells can be artificially generated via nuclear transfer or nuclear reprogramming w/ ,
distinct benefits and
disadvantages
a.
SOMATIC CELL NUCLEAR TRANSFER ( SCNT)
a an
egg
cell ( therapeutic cloning)
exigencyofexcessembryoso.ae
excess embryos raising ethical
-
→ concerns
NUCLEAR REPROGRAMMING
a a a
of ,
largely as a in
microscopy
fBEfpeM
-
"
made of cells
microscope are
ROBERT HOOKE -
"
"
of
"
the term cell
credited for developing first two
-
see
concluded that :
"
where a cell
"
"
animalcules exists there must have been
,
"
a pre -
existing cell
scientific instruments that are used to visualise objects that are too small to see w/ the
naked eye
ooopticafightmirosopesandelectronmicroscopesl.IE
There are two main types of microscope
H T M I C R O S C O P E S
lenses to bend light and magnify images by factor of roughly 100 fold
o•
use a
↳ XIOO
be used to
living in natural colour
e.
can view specimens
e.
chemical dyes and fluorescent labelling may be applied to resolve specific structures
E L E C T R O N M 1 C R O S C O P E S
be used to view dead specimens in monochrome (although false rendering may be applied )
e.
can colour
cross -
section
scanning electron microscopes (SEM) scatter electrons surface to differentiate depth and
-
over a
mapin3DL
I G H T V S E L E C T R O N M 1 C R O S C O P E S
cell scale
-1
R E L A T l V E 5 I 2 E S O F B I 0 L 0 G I C A L
M A T E R 1 A L s
→
eukaryotic cell ( plant) =nI00µm
→
eukaryotic cell (animal) =
N10 -
50µm
5µm
→
virus
=
NIOONM
→
molecules (eg glucose)=
: nlnm
→
atoms =
NIOOPM
D 1 A G R A M O F R E L AT 1 V E S C A L E O F
B I 0 L 0 G I C A L M A T E R 1 A L S
CELL STRUCTURE
cells
prokaryotic
PROKARYOTES baryon
'
nucleus before
organisms
-
=
a =
,
↳
they belong to the
kingdom Monera and have been further classified into TWO distinct
domains
:
e.
ARCHAE BACTERIA -
o.o.EUBACTERIA -
P R O K A R Y O T I C F E A T U R E s
nudeoid the
cytoplasm where the DNA
*••
region of
-
ribosome =
70s)
e.
cell membrane semipermeable and selective barrier the cell
surrounding
-
slime capsule thick polysaccharide layer protection against dedication (drying out)
e.
a used for
-
and phagocytosis
a
,
singular -
flagellum
pili hair like extensions that enable adherence to surfaces ( attachment pili) mediate bacterial
e.
or
-
In the
process of binary fission . . .
membrane
elongates and pinches off (cytokinesis) forming two cells
-
Eukaryotic cells
(
' '
EUKARYOTES '
good 1 true baryon nucleus)
'
-
[ a more
compartmentalised by
complex structure AND
membrane
are
-
believed to have evolved from
bound structures
prokaryotic cells (via
FUNGI have cell wall made chitin AND obtain nutrition via
heterotrophic absorption
a. -
a
of
a.
PLANTA E -
have a cell wall made of cellulose AND obtain nutrition autotrophically (via
photosynthesis)
•
'
ANIMAL IA -
C E L L
T Y P I C A L S T R U C T U R E O F A P L A N T C E L L
organelles
ORGANELLE -
specialised sub -
structures within a cell that serve a specific function
whereas
eukaryotic cells possess several
U N l V E R S A L O R G A N E L L E S
E U K A R Y O T 1 C O R G A N E L L E S
P L A N T C E L L S O N L Y
A N I M A L C E L L S O N L Y
Electron microscopy
↳ electron beams focused to resolve microscopic
Use
by electromagnets magnify and specimens
of
cell micrograms
MICRO GRAPH -
a photo or
digital image taken through a
microscope to show a
magnified image of
a specimen
While organelles have identifying structures , specific shapes may vary depending on the location
of cross -
sections
P R O KA RY OT I C CELL FEATURES
nuc I e o i d ce 1 I wa 1 I
i t f 1 I 1
age
i a
p
nucleus ER
i t c h o n d r i a I i
m o
g o
g
c h I o r o
p t a s t c e 1 I w a 1 I
v a c u o I e
O R G A N E L L E S
Attempts can be made to deduce cell function based on the relative abundance of various
consuming
muscle cells )
processes (e.g neurons
:
,
ER →
cells w/ extensive ER networks undertake secretory activities (e.g plasma
:
cells exocrine
, gland cells)
LYSOSOMES →
cells rich in
lysosomes tend to
undertake digestive processes
(eg phagocytes)
:
CHLOROPLASTS →
cells w/ chloroplasts undergo
photosynthesis (e.g plant leaf
:
P R O K A R Y O T I C C E L L
KEY FEATURES :
e.
PILI -
shown as
single lines
e.
FLAGELLA -
labelled as 70s
e.
CELL WALL -
SHAPE
leg
e.
for
:
a
appropriate dimensions
-
Eukaryote structure
A N I M A L C E L L
KEY FEATURES :
o•
NUCLEUS -
a.
RIBOSOMES -
labelled as 80S
e.
CYTOSOL -
( cytoplasm
'
is all internal contents
minus the nucleus)
e.
ENDOPLASMIC RETICULUM -
trough ER)
a.
MITOCHONDRIA -
double membrane w/ inner one folded into cristaei no larger than half the
nucleus in size
e.
60161 APPARATUS -
KEY FEATURES :
e.
VACUOLE -
large and
occupying majority of
central space (surrounded
by tonoplast)
e.
CELL WALL -
labelled as
being composed of
cellulose thicker than cell
,
membrane
e.
SHAPE -
brick like
-
e.
CHLOROPLASTS -
photosynthetic tissue )
extra
light microscopy
Optical microscopes use lenses to bend
light and
magnify images (extent of magnification determined
by
lenses)
a.
most light microscopes include both an ocular lens Into x) and objective lens In I0K 4OX ,
100 x )
/ / /"
FOCUS MECHANISM " " """ "
| |
STAGE CLIPS
µ, IRIS DIAPHRAGM
F U N C T I O N O F M I C R O S C O P E C O M P O N E N T S
FOCUS MECHANISM
responsible for resolving the
image (may include both fine and
a.
coarse focus
-
adjustments)
OBJECTIVE LENS
magnifies image of specimen (in conjunction w/ ocular lens)
a. -
STAGE
platform is
positioned (specimen slide)
a.
which specimen to
on is usually affixed glass
-
STAGE CLIPS holds specimen in place (some mechanical stages be moved to reposition slide
e.
can
-
while viewing)
e.
LIGHT SOURCE -
Types of cells
Prokaryotes belong to of two demain 's Archaea & Eubacteria which collectively
e.
one
-
-
form the
kingdom Monera
comprise a can -
C L A S S I F I C A T I O N O F K I N G D O M S
O R G A N I 5 A T I O N O F D O M A 1 N S A N D
K I N G D O M S
Types of bacteria
All bacteria share features common to every prokaryotic cells
a.
lack a nucleus and membrane-bound organelles
e.
have circular DNA that is naked (not bound to protein)
e.
smaller ribosomes ( 70s)
SHAPE round (coccus) rod like ( bacillus) shaped (vibrio) or spiral Ispirillal
e.
comma
-
- -
, ,
spirochaete)
-
or
( lipopolysaccharide layer)
e.
GASEOUS REQUIREMENTS -
e.
NUTRITIONAL PATTERNS -
heterotrophic
B A C T E R 1 A L S U B -
C L A S S I F I C A T I O N S
Prokaryotic vs
Eukaryotic cells
Prokaryotic cells and eukaryotic cells differ in a number of key features including :
,
e.
DNA composition and structure
e.
Reproduction mode differs according to chromosome structure
e.
P R O K A R Y O T 1 C V S E U K A R Y O T I C F E A T U R E s
mnemonic 8 DORA
Animal cells and plant cells both types of eukaryotic cells and hence share
are many common
features including :
,
a variety of membrane-bound
organelles (eg : mitochondria , ER , golgi apparatus)
-
presence or -