14 Flashcards

1
Q

How many cells are in our body?

A

37 Trillion

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2
Q

how many different cell types are in our body?

A

210

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3
Q

What are two diff microscopes that can be used with their magnification?

A

Light microscopy (2,000x)

Electron microscopy (>500,000 x)

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4
Q

What are the two main types of imaging techniques for cells?

A

Immunocytochemistry: using antibodies to pick up proteins in cell.

Immunohistochemistry: Using antibodies to identify cell structures within whole tissue cells

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5
Q

What are the two main forms of chromatins? and their characteristics?

A

Euchromatin: loosely packed so electron light so doesn’t show well on electron microscope –> transcribed

Heterochromatin: tightly packed electron dense so shows well on electron microscope

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6
Q

What is the function of the nucleolus?

A

The nucleolus makes ribosomal subunits from proteins and ribosomal RNA, also known as rRNA. It then sends the subunits out to the rest of the cell where they combine into complete ribosomes.

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7
Q

What diseases are linked with failure in structure of nucleus

A

Laminopathies ( Emery Dreifuss muscular dystrophy, hutchinson Gilford progeria syndrome)

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8
Q

What disease is linked with problems in the RER

A

Cystic fibrosis. CFTR synthesis happens in RER. CFTR protein is misfiled in the RER –> not translocated to PM.

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9
Q

What is the function of the smooth ER

A

Makes (Synthesis of) lipids and carbohydrates
Storage site for calcium (in muscle par example)
Detoxification- ER enzymes detoxify absorbed drugs toxins (liver and kidney have hgiher number of smooth than rough ER)

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10
Q

What is the difference between exocytosis an secretory vesicles

A

Exocytosis is constitutive secretion (not regulated by cell signalling)
e.g. Extra cellular matrix proteins by fibroblasts

Secretory vesicles-regulated by cellular signals e.g. Insulin-b cells in islets of Langerhans

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11
Q

What diseases are linked with lysosomal storage deficiencies=

A

Tay Sachs. Failure to break down gangliosides (lipids) so cell is clogged up –> dysfunctional.

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12
Q

Lysosomes function

A

Originate at Golgi
Contain digestive enzymes
Defense against disease (bacteria engulfed by macrophage are then taken up by lysosomes
Autophagy-cleanup of cell organelles (bc organelles have limited life expectancy)
Autolysis after cell death

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13
Q

Peroxisome function

A

originate at rough ER
metabolism of fatty acids (lipids)
detoxifying (contains enzymes that break down free radicals from normal metabolic processes, H2O2, alcohol)
Liver and Kidney

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14
Q

What diseases are linked to peroxisome deficiencies?

A

Leukodystrophies (Zellweger syndrome –> accumulate high levels of long chain fatty acids

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15
Q

What are some mitochondrial diseases

A

mitochondrial myopathies

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16
Q

What are the 3 key types of skeletal components of the cell with their sizes

A

Microfilament (3-6 nM)
Intermediate filaments (10 nM)
Microtubules (20-25 nM)

17
Q

What are some diseases linked with gamma actin mutation

A

congenital deafness

18
Q

What are some diseases linked with muscle actin mutation

A

myopathies

19
Q

What are some diseases linked with intermediate filament mutation

A

EB, laminopathies

20
Q

characteristics of Microtubules

A

cell scaffold
tracks for movement of cell organelles and vesicles (motors)
mitotic spindle fibres
cilia and flagella – locomotion
Drug targets - eg taxane anti- cancer drugs, stop cell division

21
Q

characteristics of microfilaments

A

actin proteins polymerize in all cells-cell movement
cell cytoskeleton – control cell shape (stress fibers)
cell movements with myosin (e.g. cytokinesis)
cell organelle and vesicle transport
Actin can polymerize with myosin to allow cell movement and migration
Actin filaments act as highways in the cell for organelles and vesicles
alpha actin thin filaments with myosin in muscle movement
Actin filaments are important for cell division. At cytokinesis, actin ring forms around the cell to constrict the two daughter cells.

22
Q

characteristics of intermediate filaments

A

Intermediate filaments, 10 nm, e.g. keratins in skin and hair, neurofilaments, lamins in nuclear envelope, muscle desmin
Intermediate in size between microfilaments (3-6 nM) & Microtubules (20-25nM)
Main role is to provide cell with tensile strength
Diseases e.g. keratin mutations in congenital epidermal blistering diseases – e.g. Epidermalysis Bullosa, Laminopathies