Connective Tissue Flashcards

1
Q

What are the functions of connective tissue?

A

1) Binding and supporting (such as holding skin, gut, lungs)
2) Protecting (such as bone protecting vital organs, eg. fat acting as shock absorber)
3) Insulating
4) Storing reserve fuels and cells (bone marrow and fat tissue)
5) Transporting substances within the body (blood and interstitium)
6) Separation of tissues (fascia and tendons/cartilage)

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2
Q

What is interstitium?

A

Space between tissues and organs of the body

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3
Q

What are the two types of connective tissue proper?

A
  • Loose connective tissue

- Dense connective tissue

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4
Q

What is loose connective tissue also known as?

A

Also known as areolar tissue

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5
Q

What is dense connective tissue also known as?

A

Also known as ‘fibrous’ or collagenous tissue

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6
Q

What are the two types of dense connective tissue?

A

Irregular
- Fibres running in different directions
Regular
- Fibres running in parallel to each other

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7
Q

What are the types of adipocytes?

A
  • Unilocular

- Multilocular

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8
Q

What adipocytes are found in loose connective tissue?

A

White adipocytes (unilocular)

  • Single lipid droplet, with nucleus cytoplasm and organelles all squeezed to one side of the cell
  • Acts as padding and shock absorber, insulation and energy reserve
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9
Q

What are multilocular adipocytes?

A

Brown adipocytes

  • Few of these in an adult
  • Multiple small lipid droplets with the nucleus, cytoplasm and organelles squeezed to the centre of the cell.
  • Provide insulation and energy reserve
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10
Q

What are the differences between white and brown fat tissue?

A

White adipose tissue:

  • Single lipid droplet
  • Normal number of mitochondria
  • Single peripheral nucleus
  • In adults, lipid breakdown is slow and heat is only generated after shivering reflex

Brown adipose tissue:

  • Multiple lipid droplets
  • Increased number of mitachondria
  • Single central nucleus
  • In neonates and young children, lipid breakdown is accelerated, oxidative phosphorylation is uncoupled to generate heat
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11
Q

What is collagen

A

The most common protein in the body

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12
Q

How many types of collagen are there?

A

4

  • Type I
  • Type II
  • Type III
  • Type IV
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13
Q

What is Type I Collagen?

A
  • The most widely distributed type (90%)
  • Fibrils aggregate into fibres and fibre bundles

eg. tendons, capsules of organs and skin dermis

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14
Q

What is Type II Collagen?

A

Fibrils do not form fibres

eg. present in hyaline and elastic cartilage

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15
Q

What is Type III collagen?

A

Fibrils form fibres around muscle and nerve cells and within lymphatic tissues and lymphatic organs (eg. spleen) and in tendons
- Called reticulin

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16
Q

What is Type IV collagen?

A

Unique form present in basement membranes

17
Q

What is extracellular matrix?

A

A term used to describe a complex extracellular structural network that consists of ground substances and fibres

18
Q

What fibres are found in connective tissue?

A

Collagen
- Flexible with high tensile strength
Reticular (absent in areolar tissue)/reticulin
- Provide a supporting framework/sponge
Elastin
- Allows tissues to recoil after stretch or distension

19
Q

How is collagen produced?

A
  • Fibroblasts secrete procollagen that is converted to collagen molecules outside the cell
  • The collagen molecules are then aggregated to form collagen fibrils
  • In some tissues, fibrils group together to form collagen fibres to give strength (bone, tendons, ligaments)
20
Q

What is required for procollagen production?

A

Vitamin C

- Required for intracellular production of procollagen, where it hydroxylates proline and lysine

21
Q

What happens with a vitamin C deficiency?

A

-Disrupts collagen formation leading to scurvy

22
Q

What happens in scurvy?

A
  • The thin collagen fibrils aggregate in some areas to form thicker collagen fibres
23
Q

What are the symptoms and signs of scurvy?

A
  • Gum disease and tooth loss
  • Bruising of the skin and hair loss
  • Bleeding
  • Poor wound healing
  • Weakness and fatigue
  • Impaired bone development in the young
24
Q

What is Marfan’s syndrome?

A
  • Autosomal dominant disorder

- Expression of the fibrillin 1 gene is affected so elastic tissue is abnormal

25
Q

What are signs and symptoms of Marfan’s syndrome?

A
  • Abnormally tall and large wingspan
  • Arachnodactyly (long fingers and toes)
  • Frequent joint dislocation
  • At risk of catastrophic aortic rupture
26
Q

What is the primary component of elastic fibres?

A

Elastin

- Elastin infolds and is surrounded by microfibrils of fibrillin

27
Q

Where are elastin fibres found in the body?

A
  • Dermis
  • Artery walls
  • Lungs
  • Sites bearing elastic cartilage
28
Q

What is Osteogenesis Imperfecta?

A

‘Brittle Bone Disease’

29
Q

What causes Osteogenesis Imperfecta?

A
  • Mostly autosomal dominant

- Due to mutated collagen fibres that do not ‘knit together’