Cellular structure/processes Flashcards

1
Q

What the cell structure basics

A

basic structural, biological, functional units that comprises an organism

Smallest self-replicating life-form

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2
Q

The main levels of organization in the body, from the simplest to the most complex are:

A

Cells > tissues > organ > organ system > organism

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3
Q

What are the basic constituents of cells

A
  • Plasma membrane
    • Cytoplasm: everything in cell membrane except nucleus)
  • Fluid suspension
    • Composition: cytosol (liquid found inside of cells), organelles
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4
Q

What is the Cytosol?

A

Intracellular fluid

  • Composition: dissolved/suspended organic, inorganic chemicals; macromolecules; pigments; organelles are in the cytosol
    • the cytosol is the fluid surrounding it.
  • Site of most cellular activity.
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5
Q

Where is the site of most cellular activity?

A

The Cytosol (in cytoplasm)

Site of most cellular activity

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6
Q

What is the composition of ribosomes?

A

rRNA, ribosomal proteins

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7
Q

Where can you find ribosomes

A

Can exist freely in the cytoplasm/bound to endoplasmic reticulum (forms rough endoplasmic reticulum)

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8
Q

What is the purpose of ribosomes

A

Turns mRNA into protein via translation

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9
Q

What subunits are ribosomes organised into?

A
  • Organized into two subunits (40’s, 60’s)
    • Small subunit: binding sites for mRNA, tRNA
    • Larger subunit: has ribosome to catalyse peptide bond formation (for bonds between amino acids)
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10
Q

What is the endoplasmic reticulum?

Also, what is its appearance?

A

membrane-enclosed organelle

Appearance: a stack of membranous. Flattened disks (cisterns)

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11
Q

Rough endoplasmic reticulum (RER) structure

A

Contain bound ribosomes on the surface

Rough endoplasmic reticulum cisterna continuous with nuclear envelope.

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12
Q

What is the function of Rough endoplasmic reticulum

A

Site of packaging, folding of proteins Designated for secretion, lysosomal degradation,
plasma membrane insertion, proteins packed into vesicles, sent to Golgi apparatus for further modification

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13
Q

Smooth endoplasmic reticulum structure

A

No ribosomes

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14
Q

Smooth endoplasmic reticulum function

A

Site of making lipids, steroid synthesis (Glans), ions storage (muscles), glycogen metabolism, Detoxification (liver).

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15
Q

Golgi apparatus purpose/function

A

Golgi apparatus

Post-translational modification site (e.g. phosphorylation, glycosylation, sulfonation) of proteins, lipids hormones
→ sorted, packed into secretory vesicles → secreted out of cell/lysosomal fusion/plasma membrane insertion

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16
Q

Golgi apparatus Structure

A

Membrane-enclosed organelle

Appearance: a collection of fused, flattened sacs (cisterns) with associated vesicles, vacuoles

Two sides

Cis-side: receives proteins from Rough endoplasmic reticulum (entry)

Trans side: opposite side, releases vesicles towards the plasma membrane (Exit)

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17
Q

what are the Golgi apparatus side(s) functions

A

Two sides

Cis-side: receives proteins from Rough endoplasmic reticulum (entry)

Trans side: opposite side, releases vesicles towards the plasma membrane (Exit)

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18
Q

Mitochondria Structure

A

Double membrane-enclosed organelle;

Outer smooth membrane: Inner membrane:

Inner membrane space: space between the inner, outer membrane

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19
Q

Mitochondria Purpose

A

synthesizes ATP for cell via aerobic respiration

In cytoplasm glucose undergoes glycolysis, glucose is cleaved into pyruvate.

Pyruvate enters mitochondria > citric acid cycle (Krebs cycle), electron transport chain (which require oxygen)

In glucose absence, mitochondria can use fatty acids as fuel via beta-oxidation (only medium-sized fatty acids used; longer ones chopped by peroxisome)

Mitochondria number: correlates with cell activity/energy/requirements.

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20
Q

Nucleus Structure

A

Large, membrane-enclosed organelle present in all cells except mature erythrocytes (RBC)

Most cells contain one nucleus; some cells have more (e.g. muscle cells, osteoclasts, hepatocytes)

Usually spherical, may take on other shapes

Lobulated (e.g. polymorphonuclear leukocytes)

Elongates (e.g. columnar epithelium)

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21
Q

Nucleus purpose

A

Contains genetic material (DNA, tightly packed into chromatin); coordinates cellular activities

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22
Q

Cell membrane structure

A

Semipermeable membrane made from phospholipid bilayer; surrounds cell cytoplasm

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23
Q

Cell membrane: phospholipid bilayer structure

A

Two-layered polar phospholipid molecules comprising two parts

Negatively charged phosphate “head” (hydrophilic; orientated outwards)

Fatty acid “tail” (hydrophobic orientated (inwards)-

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24
Q

why is the phospholipid layer Semipermeable?

A

Allows passage of certain molecules through the membrane (02, C02 etc)

Denies passage of others (large molecules such as proteins, glucose)

Certain molecule transportation (Ions, H2O) allowed through embedded membrane proteins (ion channels, pumps)

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25
Q

What is meant by “Selective permeability of the cell membrane”

A

Cell membrane controls which molecules enter and leave:

Passive transport:

Active transport: energy is required

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26
Q

In relation to energy, What is passive transport?

A

Passive transport: no energy required to pass cell membrane

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27
Q

In relation to energy, What is Active transport:

A

Active transport: energy is required to cross cell membrane = adenosine triphosphate (ATP)

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28
Q

Explain passive transport

A

Simple diffusion

Random molecular motion

Small nonpolar molecules move from high concentration -> low concentration

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29
Q

What affects diffuse flux (Ficks law)

A

Three factors

Concentration gradient

  • Larger differences in solute concentration on each side of the membrane -> high driving force -> high net diffusion
  • Equal concentrations -> no net diffusion (e.g. , movement between alveoli and blood)

Membrane surface area

  • Increase surface area available for diffusion -> increase diffusion rate; vice versa (e.g. microvilli in small intestines amplify the surface area -> increase nutrient, water distribution)

The distance separating each side of the membrane (e.g. thickness)

  • Increase distance molecules must travel -> decrease of net diffusion; vice versa (e.g. pulmonary oedema -> increase distance between compartments -> decrease net diffusion)
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30
Q

How does concentration affect diffuse flux? (Ficks Law)

A

Concentration gradient

Larger differences in solute concentration on each side of the membrane -> high driving force -> high net diffusion

Equal concentrations → no net diffusion (e.g. , movement between alveoli and blood)

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31
Q

How does membrane surface area affect diffuse flux (Ficks law)

A

Membrane surface area

Increase surface area available for diffusion -> increase diffusion rate; vice versa (e.g. microvilli in small intestines amplify the surface area -> increase nutrient, water distribution)

32
Q

How does The distance separating each side of the membrane affect diffuse flux (Ficks law)

A

The distance separating each side of the membrane (e.g. thickness)

Increase distance molecules must travel -> decrease of net diffusion; vice versa (e.g. pulmonary oedema -> increase distance between compartments -> decrease net diffusion)

33
Q

What is Facilitated diffusion?

A

Uses transport proteins (e.g. channels, carrier proteins)

Allows larger/polar molecules to move across the membrane

34
Q

What are Channels on the cell membrane?

A

Non-specific, open to allow water, small polar molecules through (e.g. voltage-gated calcium channel)

35
Q

What are Carrier proteins on cell membranes

A

Very specific, only allow certain molecules to bind (e.g. glucose transporter (GLUT4)

36
Q

Explain primary active transport

A

Primary

Uses ATP

Enzymes called ATPases use ATP as fuel; (e.g. Na+/K+-ATPase, ATPase, H⁺/K⁺ ATPase)

May create concentration/electrochemical gradients

37
Q

Explain secondary active transport

A

Secondary

Uses existing electrochemical gradients

One solute, normally Na+ moves with concentration gradient through transporter -> supplies energy transporter needs to -> another solute against concentration gradient in same/opposite direction as Na+ (e.g. sodium-glucose SGLT1 transporter)

38
Q

Explain Bulk transport

A

AKA vesicular transport

Endocytosis

Cell membrane invaginates, pulling something in from outside e.g. pathogen phagocytosis)

Exocytosis

Vesicle inside cell pushes something (e.g. hormone secretion)

39
Q

What is the Extracellular Matrix

A

The environment surrounding the cells

Varies between tissues (epithelial, connective, and nervous)

40
Q

What are the major molecules in the extracellular matrix?

A

Adhesive proteins

Structural proteins

Proteoglycans

41
Q

What are Adhesive proteins

A

Adhere cells together (communication with extracellular fluid)

e.g. integrating cadherins

42
Q

What is the purpose of Structural proteins?

A
  • Give tissues tensile, compressive strength
  • Collagen
    • Resists tension, can stretch
    • Starts as procollagen → cleaves into tropocollagen → arranged into fibrils
    • Four major types of structural proteins: type 1(bone, skin, tendon). Type 2 (cartilage), type 3 (reticulin, blood vessels), Type 4 (basement membrane)
  • Elastin
    • Elastic, returns tissue to original shape
  • Keratin
    • Tough, found in hair and nails
43
Q

What are Proteoglycans?

A

Fill space between cells, hydrate, cushion cells

Consists of a protein core with sugar chains

44
Q

What is the purpose of Cell-Cell junctions

A

Protein structures that physically connect cells

Improve cellular communication, tissue structure; allow transport of some substances between cells, create an impermeable barrier for others

Only found between immobile cells; abundant in epithelial tissue (e.g. in the skin)

45
Q

What are the three junction types?

A

Tight junctions

Adherens junctions

Gap junctions

46
Q

What are Tight junctions?

A

e.g. in the gastrointestinal tract/brain

Seal adjacent-cell plasma membranes, especially near the apical surface; prevent the passage of water. Small proteins, bacteria Formed by claudins, occluding embedded in cellular plasma membranes

In “leaky” epithelia, tight junctions may allow certain molecules to pass (e.g. K+. Na+, -CL in kidneys proximal tubules - due to ion pores)

47
Q

What are Adherens junctions?

A

e.g. in skin

Anchor cells together, provide strength; consist of three major components

Actin filaments: provide cellular shape

Protein plaques: anchor membrane bind to actin filaments

Cadherins: attach to protein plaques, connect to cadherins on other cells.

48
Q

What are Gap junctions?

A

E.g. in heart

Connect adjacent cells, allow rapid communication; formed by connexins -> create tubular structure (allows charged particles to pass)

In cardiac myocytes: gap junctions create coordinated heart contractions

In infected cells: gap junctions send cytokines to neighbouring cells, triggering apoptosis, preventing infectious spread (“bystander effect”)

49
Q

Endocytosis and exocytosis

A

ransports material in/out of cell

Requires adenosine triphosphate (ATP) for energy

50
Q

What does endocytosis do?

Three types are:

A

Cell engulf extracellular material

Three types are: phagocytosis, pinocytosis & receptor-mediated endocytosis

51
Q

What does phagocytosis do?

A

Aka cell eating

Used by white blood cells (e.g. macrophages, neutrophils)

Process:

  • The cell extends arm-like projects (AKA pseudopods) around the target
  • Cell membrane slowly engulfs target, invaginates to form a vesicle
  • Vesicle separates from cell membrane to form a phagosome
  • Phagosome fuses with lysosome, target is digested
  • Debris released by exocytosis
52
Q

What is pinocytosis

A

Aka cell drinking

Edges of invagination come together to form a vesicle

Motor proteins use ATP to carry vesicles into the cytosol

53
Q

What is receptor-mediated endocytosis?

A

Used by cells to take in specific molecules (e.g. iron, cholesterol)

Process

  • Clathrin-covered pits/coated pits with receptors bind certain molecules
  • Edges of put come together, clathrin proteins link up
  • Vesicle pinches off; clathrin detaches, return to the cell membrane
  • Vesicle merges with endosome to separate receptors into the second vesicle
54
Q

What is Exocytosis?

A

Cells expel material into extracellular space (e.g. neurotransmitters, hormone)

Last phagocytosis step

Process

  • Golgi apparatus creates vesicle from various proteins, lipids, hormones
  • Motor proteins use ATP to carry vesicle along cytoskeleton
  • Vesicle pressed against cell membrane until rupture -> spills contents into extracellular space.
55
Q

What is Osmosis?

A

Passive water-flow across selectively permeable (semipermeable) cellular membrane; primarily determined by solute concentration differences (osmotic pressure)

56
Q

Factors affecting water movement across the membrane?

A
  • Molecules (e.g. water molecules, ions) tend to move around kinetic energy) + movement is disordered, random (entropy) → larger solutes tend to block openings in a semipermeable membrane
  • If solute ions positively charged, they attract slightly negatively charged oxygen atoms in water molecule; if solute ions are negatively charged they attract slightly positively charged hydrogen atoms in water molecule

→ water molecules partially attached to the ion

→ movement through membrane impeded

  • Water molecules tend to move from hypotonic side (more water/less solutes) to hypertonic side (less water/more solute)
57
Q

What relation does the selectively permeable membrane have on Osmosis?

A

Allows small molecules (e.g. water) across, but not larger molecules/ions

58
Q

In an isotonic solution..

A

Side A= Side B

If solute concentration is the same on each side of membrane -> net water movement across membrane is zero (equilibrium)

59
Q

In Hypertonic/hypotonic solution….

A

Side a> side B or Side B >Side A

If the solute concentration is greater on one side (hypertonic) -> net water migration across the membrane is from the hypotonic side toward the hypertonic side

60
Q

Cellular effects on hypertonic, hypotonic solution

A

Red blood cells in hypertonic solution → net movement of water molecules out of cell → cell shrinks (cremation)

Red blood cell in hypotonic solution→ net movement of water molecules into cell → cell swells may burst (lyses)

61
Q

Resting membrane potential: Electric potential across cell membrane

A
  • Given weighted (based on membrane permeability) sum of equilibrium potentials for all ions.
  • High concentrations of Na+, -Cl, Ca+ outside the cell; high concentrations of k+, -A (various anions) inside cell -> concentration gradients are established Sodium-potassium pump uses ATP to move two K+ ions into cell, three Na+ ions out.
  • Potassium concentration = 150mMol/L inside cell, 5mMol/L outside cell.
62
Q

Resting membrane potential: Concentration gradients

A

Concentration gradients establish electrostatic gradients

  • Concentration gradient pushes potassium out through potassium leaky channels, inward rectifier channels
  • Anions remain in cells -> negative charge builds up -> potassium is pulled back into cell.
63
Q

Resting membrane potential: Equilibrium (Nernst) potential:

A

Equilibrium (Nernst) potential: electrostatic gradient equal to concentration gradient (-92mV for potassium)

Value is flipped for negative ions

Resting membrane potential is sum of equilibrium potentials of major ions multiplied by their membrane permeabilities.

64
Q

Cell signalling pathway stages

A

Cell signalling pathway stages

  • Reception: ligand binds to receptor
  • Transduction: receptor changes activating intracellular molecules
  • Response: signal triggers a response in target cell
65
Q

Ion channel receptors

A

Ion channels that open specific ligands bind

Allow ions (e.g. chloride, calcium, sodium, potassium) to flow through

The resulting shift in electrical charge distribution triggers a response

66
Q

cytoskeleton & intracellular motility

A

Non-membrane bound organelles comprising complex protein filament network

Provide structural stability, shape, organisation, intracytoplasmic motility, cell motility

67
Q

Cytoskeleton protein filament network Types

A

Microfilaments

Microtubules

Intermediate filaments

68
Q

Nuclear Envelope

A
  • Encloses separates the nucleus from the cytoplasm
  • Composed of the selectively permeable membrane phospholipid bilayer

Consists of:

  • Nuclear pores
  • Outer membrane
  • Inner membrane
69
Q

Nuclear pores:

A
  • Form where membranes fuse together at various intervals
  • Each pore is lined with a nuclear pore complex (nucleoporin) to facilitate communication between the nucleus, cytoplasm
  • Allow bidirectional macromolecule movement
70
Q

Outer membrane

A

Anchoring proteins that hold nucleus in place with cytoplasm

Continuous with rough endoplasmic reticulum

71
Q

Inner membrane

A

Covered by the nuclear lamina

Thin filamentous protein network, creates web within the nucleus; provide support for chromatin

72
Q

Nucleosome

A

Eight histones packed together in four stacks of two; DNA wraps around them twice

Strung on strand of DNA-like “beads on string”

73
Q

Two chromatin types

A

Euchromatin: loosely packed DNA, actively being transcribed into RNA

Heterochromatin: densely packed DNA, inactive (not being transcribed)

74
Q

Nucleolus

A
  • Dense non-membrane-bound structure; some cells have more than one nucleolus
  • Contains rDNA -> transcribes into rRNA
  • Assembles ribosomal subunits
75
Q

Nucleoplasm

A
  • Protoplasmic material
  • Composed of complex water, molecule, ion mixture
  • Contains nucleolus, chromatin
76
Q

Chromatin

A
  • Helical fibre
    • Composed of 46 DNA molecules wrapped around proteins (histones)
  • Histones help regulate DNA, gene expression
  • Chromosomes become visible as chromatin fibres become tightly coiled during cellular division
77
Q
A