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Cell tissue and structure - lecture II

Anna Hogarth Fudamentals of Medicine Inglés 67 fichas

Cell tissue and structure - lecture II

Fichas del conjunto (67)

  1. 1Define connective/supportive tissueA tissue that lies between two other tissues, consists of cells and ECM
  2. 2What are the four kinds of connective tissue?1) Loose connective tissue - e.g. serous membranes, blood and adipose.
    2) Dense connective tissue - dermis of skin
    3) Bone
    4) Cartilage
  3. 3What are the five different cells which synthesis ECM?1) Fibroblast
    2) Adipocyte
    3) Chondrocytes
    4) Osteocytes
    5) Haemopoeitc
  4. 4What does the ECM determine?Physical properties of tissue
  5. 5List the five roles of ECM?1) Cell migration
    2) Shape
    3) Proliferation
    4) Survival
    5) Tissue development
  6. 6Describe the secretion of ECMConstitutive secretion - not tightly controlled
  7. 7How is the nature of a tissue changed?ECM is altered with development.
  8. 8What are the qualities of the dermis and why is this important?Elastic and strong so that shearing forces don't cause damage.
  9. 9Describe the ECM of: 1) Bone 2) Neural tissue 3) Tendons 4) Dermis1) Abundant calcified ECM
    2) Almost no ECM
    3) Tough, rope-like ECM
    4) Pliable, acts as a shock absorber
  10. 10LIst the components you would expect to find in the dermis (6)1) Collagen fibres
    2) Macrophages
    3) Capillaries
    4) Mast cells
    5) Elastic fibres
    6) Fibroblast
  11. 11What separates the dermis from the epithelial layer (epidermis)?Basement membrane
  12. 12What is a proteoglycan? Where are they assembled and how are they secreted?1) A proteoglycan monomer consists of a protein core with many glycosaminoglycans attached
    2) Proteoglycans are assembled in the ER and Golgi and are delivered to the ECM via secretory bodies (constitutive secretion)
  13. 13What is the primary function of GAGs and proteoglycans?They can bind water and form hydrated gels, filling the space between cells. This can function to lubricate joint cavities as well as resisting compressive forces.
  14. 14Other than resisting compressive forces and lubricating joint cavities, what do GAGs ad proteoglycan gels facilitate?Permit the rapid diffusion of nutrients, hormones and metabolites.
  15. 15What is a glycosaminoglycan (GAG)?A linear chain of 20-100 dissaccharides
  16. 16What modification has usually been made to disachharides?Usually sulfated
  17. 17Give three examples of GAGs1) Chondroitin sulfate
    2) Heparin sulfate
    3) Dermatan Sulfate
  18. 18Give two examples disaccharides which are found in GAGs1) Iduronic acid
    2) N-acetylgalactosamino-4-sulfate
  19. 19What is hyaluronic acid?A glycosaminoglycan which consists of 25,000 disaccharides
  20. 20Why is it important that cells can migrate through hyaluronic acid? How can this be exploited clinically?1) Important for wound healing
    2) Can use a synthetic dermis consisting of HA to encourage cell migration and dermal healing
  21. 21Give three examples of proteoglycans1) Biglycan
    2) Syndecan
    3) Aggrecan
  22. 22Of the three examples listed previously, which is the longest? Which is attached to the plasma membrane?1) Aggrecan is much longer than biglycan and syndecan
    2) Syndecan
  23. 23Which GAGs make up: 1) Aggrecan 2) Syndecan 3) Biglycan1) Chondroitin sulfate chains and keratin sulfate chains. Can attach through a linker protein to hyaluronan
    2) Heperin sulfate chains
    3) Dermatan sulfate chains
  24. 24Which is the most abundant protein in the human body? What is its primary function?Collagen - makes up 1/3 to 1/4 of protein in the body.
    Provides tensile strength
  25. 25How many different types of collagen are there? Which is the most common?1) 20
    2) Type 1
  26. 26What makes up the basement membrane?Type III collagen (reticulin), type IV collagen, laminin, fibrin and ground substance.
  27. 27What is orthogonal collagen?Collagen which runs in perpendicular bundles to increase tensile strength.
  28. 28What is elastin? What does it form? Where is it commonly found?1) A fibrous protein: polymer of tropoelastin associated with fibrillin (glycoprotein)
    2) Elastic fibres
    3) Arteries
  29. 29What is Marfin syndrome?1) Fibrillin gene mutation which results in ruptured arteries.
  30. 30What is Ehlers-Danlos syndrome?Can be inherited (autosomal dominant or recessive) or occur due a mutation during the early years. Can affect more than a dozen of genes - usually affects the structure, productions, or processing of collagen or proteins associate with collagen. Results in elasticated skin, loose joints, abnormal scar production, chronic pain, or early osteoarthritis.
  31. 31What causes wrinkles?Breakdown of collagen and elastin, often as a result of sun damage.
  32. 32Where are fibronectin fibres found in the body?In the ECM: circulating soluble fibronectin fibres in plasma and body fluid
  33. 33What are the functions of fibronectin? (3)1) Binds cells (integrins) and ECM (collagen)
    2) Cell attachment and matrix organisation
    3) Guides cell migration - important for development and wound healing
  34. 34What does the basement membrane underlie?1) Epithelial and endothelial cells
  35. 35What is the function of the basement membrane?Separates epithelial/endothelial cells from underlying connective tissue.
  36. 36What two components make up the basement membrane? How does the basement membrane connect to epithelial cells?1) Lamina lucida and lamina densa
    2) Hemidesmosome
  37. 37What roles does the basement membrane have? (6)Supportive, anchoring, protective role, selective cell movement, molecular filtering, signalling, and helps to prevent oncogenesis (Prevents contact with the underlying connective tissue).
  38. 38What is the underlying connective tissue under the basal lamina?Reticular tissue
  39. 39What makes up the basal lamina/basement membrane?Type IV collagen, heparan sulfate proteoglycan, laminin, and nidogen (entactin).
  40. 40Which laminin in the basal lamina connects to integrin in the epithelial cells?Laminin 10
  41. 41What is Junctional Epidermolysis Bullosa?A genetic disease which effects laminin in the basement membrane. Causes the skin to blister as the epidermis and the dermis separate. N.B. this is similar to epidermolysis bullosa where the mutation is within keratin.
  42. 42How does a carcinoma in situ turn to malignant cancer?Cancerous cells pass through the basement membrane and enter the bloodstream - metastases
  43. 43What are the different types of junctions (and their functions)? (superior to inferior)Between adjacent epithelial cells
    1) Tight/separate - prevents the passage of molecules across the epithelium
    2) Adherens - Tether adjacent cells together
    3) Desmosomal - Resist mechanical stress (strongest junction, abundant in the skin)
    4) Gap - allow passage of small molecules between adjacent cells
    Between epithelial cells and basement membrane
    1) Hemidesmosome/focal adhesion - Anchor epithelium to basal lamina
  44. 44In histology exams which tissue will usually be used to demonstrate junctions?Gut epithelia - easiest to see
  45. 45Why is it important that there is a seal between epithelial cells?Transfer from lumen into organ is ideally through a cell as this is a controlled process
  46. 46—1) Tight junction by villi
    2) Adherens - gap and reasonably dense borders
    3) Desmosome - very dense border
    1) Tight junction by villi 2) Adherens - gap and reasonably dense borders 3) Desmosome - very dense border
  47. 47—Gap junctions - note that it looks like 3 linesGap junctions - note that it looks like 3 lines
  48. 48—HemidesmosomeHemidesmosome
  49. 49What does desmosome related disease result in?Compromised cardiac and/or cardiac function
  50. 50Give an example of an infectious disease targeted at desmosomesStaphylococcus - scalded skin syndrome, bacterial proteases directed as desmosomal cadherins causing epidermal blisters.
  51. 51Give an example of an autoimmune disease directed at desmosomesPemphigus vulgaris - antibodies directed against desmosomal cadherins causing epidermal blisters.Give an example of an autoimmune disease directed at desmosomes
  52. 52What is desmoplakin? Which genetic disease can it contribute to?Protein which contributes to desmosome structures in cardiac muscle and epidermal cells. Mutation in Naxos disease - causes skin blisters, 'wooly' hair and cardiomyopathy.
  53. 53Where are primary (non-motile) cilia found? What is there function?1) Nearly all cells (usually one long cilia).
    2) Function as sensory antennae - chemosensors, photosensors, mechanosensors; signalling - Hedgehog and wnt signalling are involved in cancer developement
  54. 54Where are motile cilia found?Trachea and fallopian tubes - help move mucus and germinal cells respectively
  55. 55How do flagella compare to cillia?Flagella - much longer than cilia, propel sperm cells
  56. 56Describe the cytoskeleton of cilia and flagellaMicrotubule based cytoskeleton - axoneme (circular structure, for primary cilia this a ring of 9 microtubule doublets; for motile cilia this consists of 9 outer microtubule doublets with two central microtubules - 9+2 axoneme)
  57. 57Give three examples of genetic ciliopathies1) Bardet-Biedl Syndrome - characterised principally by obesity, retinitis pigmentosa, polydactyly, hypogonadism and renal failure in some cases
    2) Polycystic kidney disesae
    3) Lack of cilia in fallopian tubes - ectopic pregnancy
  58. 58What are psuedopodiaCell protrusions - actin polymerisation for movement. Found on neutrophils.
  59. 59What affect do amoeboid cancerous cells have on cancer prognosis?These are highly migratory and greatly worsen the prognosis
  60. 60What are lamellipodia and filopodia important for?Cell movement, contact and environmental sensing
  61. 61What are the structures that lamellipodia generally referred to as? What type of cells use them?1) Ruffles
    2) Fibroblast cell migration (wound healing) and epithelial cells
  62. 62What are the structures that filopodia form commonly referred to? Which cells use them? What are they predominantly for? When are they abundant?1) Spikes
    2) Migrating neural growth cones (if the filopodia don't make contact the cells tend to die) and fibroblasts
    3) Environmental sensing
    4) Abundant filopodia are found in invasive cancer cells
  63. 63What are microvilli? Where are they commonly found?1) Cell surface extension of secretory and absorptive cells
    2) Kidney and intestinal cells
  64. 64How many microvilli are found on the apical surface of a single small intestinal cell? What affect does this have on surface area?1) Several thousand
    2) ~600 fold
  65. 65Describe the structure of microvilliAmorphous densely staining region-digestive enzymes, outer plasma membrane and polymerised actin filament bundles within. Terminal web at the base. Much more of an internal structure than cilia.
  66. 66What causes persistent osmotic diarrheaInfection by enteropathogenic Escherichia coli, leads to malabsorption and consequently persistent osmotic diarrhea.
  67. 67What effect do toxins have on intestinal microvilli?Leads to destruction of intestinal microvilli and intestinal tight junctions resulting in the inhibition of water re-absorption.

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Professor Mike Philpott 03.10.17
Creado por
Anna Hogarth
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