Specialised tissues Flashcards

1
Q

State the function of hair

A

-Protection -Sensation -Thermoregulation

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2
Q

Outline the differences between lanugo, terminal and vellus hair

A

LANUGO >fine and long, foetus at 20 weeks >shed before birth >premature babies and anorexics TERMINAL >long, thick dark >scalp, brows/lashes, pubic, axillary, beard >begin as vellus, differentiation triggered by androgens during puberty VELLUS >short, fine, light >covers body

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3
Q

Describe the structure of a hair follicle

A
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4
Q

What is the development of hair throughout life?

A
  1. Anagen = Growth, 85% of hair, higly vascularised and energy intensive
  2. Catagen = Cell division slows/stops, end of shaft keratinises +forms club shape, dermal papilla/club moves towards base of muscle insertion
  3. Telogen = Shedding hair, club hair takes 4-6 weeks to be released
  4. Anagen begins again

ACT!!

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5
Q

How does testosterone effect hair follicles?

A

Changes vellus into terminal hair

Pubic/axillary, then beard and chest, then (in elderly) nose and ear.

Scalp has androgen sensitive hair = determines balding pattern

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6
Q

What are the functions of nails?

A
  • Protection
  • Touch
  • Communication
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7
Q

Outline the structure of nails

A

Longitudinal ridging

Grow from germinal matrix

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8
Q

Describe the growth of the nail plate

A
  1. Nail produced by proximal nailbed
  2. grows out due to adhesion
  3. Top of plate = produced by proximal portion of matrix
    * can grow up to 1 week post-mortem*
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9
Q

List the cells of the nervous system (BUMP)

A

BIPOLAR = 2 axonal projections from the cell body

UNIPOLAR = 1 axonal projection

MULTIPOLAR = Pyramidal - pyramid shaped cell body, Purkinje, GABA neurons in the cerebellum, Golgi - GABA neurons in the cerebellum

PSEUDOUNIPOLAR = 1 axonal projection that divides in 2

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10
Q

Recall the main components of a neurone

A

Cell body/soma

>Nucleus and ribosomes

>Neurofilaments for transport and structure

Dendrites

>Non-myelinated

>receives signals + highly branched

Axon

>Origionats from axon hillock at soma

>covered in myelin

>can branch into collaterals

Terminal buttons

Myelin sheath

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11
Q

State some cells of the central nervous system

A

Astrocytes = Most abundant cell, repair/homeostasis/immunity proliferation

Oligodendrocyte = Myelinates many axons

Schwann cell = Myelinates 1 axon (peripheral nerves)

Microglial cells = immunological surveillance of the CNS

Ependymal cells = line fluid-filled ventricles, regulation and production of CSF

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12
Q

How is the resting potential maintained?

A

Transportation of ions in regulated by channels and pumps.

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13
Q

Describe the creation of an action potential

A

RMP = voltage-gated channels closed

Depolarisation = Na+ channel opens, influx

Repolarisation = K+ opens at slower rate, efflux from cell

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14
Q

Explain what happens at a synapse and the 2 fates of neurotransmitters

A
  1. action potential reaches the presynaptic terminal
  2. Ca2+ channel opens
  3. Neuro vesicles exocytosis
  4. Bind to post-synaptic receptors

FATE OF NEUROTRANSMITTER: enzyme metabolism, recycled by transporter protein

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15
Q

Recall the ultrastructure of skeletal muscle

A

Z line = made up of a-actinin and CapZ

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16
Q

Explain the process of excitation-contraction coupling

A
  1. Action potential prpagates along sarcolemma and T-tubules
  2. Depolarisation activates DHPR (Dihydropyridine receptors = conformational changes
  3. change is transmitted to RyR (ryanodine receptors) on sarcoplasmic reticulum
  4. Opening of RyR and Ca2+ release = depolarisation = increase in Ca2+
17
Q

What are the components of myofibres?

A

T-tubules = membrane invaginations that contactwith extrcellular fluid

Sarcoplasmic reticulum = Network of Ca2+ stores surrounding myofibrils

18
Q

Outline the components of a sarcomere

A

z line = lateral boundaries of sarcomere

Actin = polymeric thin filaments composed of 2 twisted a helices (displays polarity)

Myosin = Thick filaments, motor proteins with globular heads

Titin = spring-like filaments anchoring myosin to z line

Nebulin = large filaments associated with actin

Tropomyosin = elongated protein bound to actin

Capz(+) and tropomodulin(-) charged ends of actin

19
Q

Describe the cellular mechanism of a contraction (sliding filament theory)

A

IN THE PRESENCE OF Ca2+

  1. Movement of troponin exposes myosin binding site on actin chain
  2. charged myosin headbinds to site
  3. Powerstroke due to binding and discharge of ADP. Pull actin towards the centre of sarcomere
  4. ATP binds = release of myosin head
  5. ATP hydrolysis = energy for myosin head
20
Q

Explain the function of skeletal muscle

A

Interaction with external environment

Antagonist pairs have flexor and extensor

myofibre bundles (cylindrical and multimucleated)

Isotonic contraction: change length, tension is the same

>Concentric = shortening

>Eccentric = Lengthening

Isometric contraction: Increase tension, length is unchanged

21
Q

Explain the structure and function of cardiac muscle

A
  • Pumps blood around the body
  • composed of cardiomyocytes (striated muscle)

>Intercalated disks: specialised regions connecting cardiomyocytes. Gap junctions to allow AP to spread

>Sarcomeres: contractile units of cardiomyocytes, contraction is the same as skeletal muscle

22
Q

Describe cardiac excitation-contraction coupling

A
  1. AP propagates along scarcolemma and t-tubules
  2. Depolarisation opens VGCC = Ca2+ influx
  3. Ca2+ = depolarisation - initiate contraction by binding to troponin - CICR (Ca2+ induced Ca2+ release) by binding to RyR on SR
  4. Depolarisation = increase in intracellular Ca2+ = contract
23
Q

Explain the structure and E-C coupling of smooth muscle

A
  • Spindle shaped cells
  • Irregular arrangment of actin/myosin
  • Present in walls of hollow organs (blood vessels, GI tract)
    1. Depolarisation activates VGCC
    2. CaM complex = activates myosin light chain kinase (MLCK)
    3. MLCK phosphorylates myosin light chains (MLC20)
    4. Cross-bridges with actin filaments = contraction
24
Q

Summarise the functions of the skin

A
  • Protection against injury and pathogenic organisms
  • waterproofing and fluid conservation
  • Thermoregulation
  • Protection agaisnt radiation, sbsorption or UV and vit D production
  • Surface for grip
  • Sensory organ
25
Outline the structure of the skin
EPIDERMIS: - Stratum Corneum = corneocytes (flat + no nuclei), defects=eczema (filagrin mutation) - Stratum Granulosum - Stratum Spinosum = Prickle (spinous, keratin producing) cell, desmosomes - Stratum Basale = Basale cells, connect to basement membrane, keratinocytes - Stratum Lucidum
26
Explain the development, function and control of melanocytes
- Originates from neural crest - surround keratinocyte in stratum basale 1 melanocyte + 36 keratinocyte -melanocytes = melanin = melanosomes
27
Summarise the components of the dermis
SUPPORTIVE CONNECTIVE TISSUE MATRIX \>Collagen (70%), elastin, glycosaminoglycans (GAGs) \>Fibroblasts \>Immune cells \>Blood vessels, lymphatics
28
Outline epithelial organisation
- create an organised, stable cell to cell junctions = continuous, cohesive layers - layers line internal and external surfaces (function: transport, absorption, secretion, protection
29
Describe cell-cell junctions in epithelia
- Arranged as continuous belts (zonulae) or discrete spots (maculae) - apical junctional complex with a tight junction nearest the apex then adhesion belt, then desmosomes throughout the lateral membrane - gap junctions are regions of direct communication with adjacent cells
30
Explain the classification of epithelia
- Simple squamous (single flat layer) e.g. lung alveolar epithelium, mesothelium + endothelium - simple cuboidal e.g. lining kidney collecting duct - simple columnar (pillar shaped) e.g. enterocytes, intestinal absorptive - stratified squamous (multiple flattened layers) e.g. keratinising - epidermis of skin, no nuclei, non keratinising - lining of mouth oesophagus and anus, viasble nuclei - psudostratified (falsely stratified) e.g. airway epithelium, urinary and reproductive ducts (often ciliated)
31
How does epithelia function?
- Requires plasma membrane polarity to give direction Apical and basolateral domains are biochemically and functionally distinct \>have different lipid and protein compositions \>separated by belt junctions
32
What is the importance of epithelial polarity in transport?