5- Cell Biology Of The Lungs Flashcards

1
Q

How many generations of dichotomous branching are there and which make up the 3 sections of the airways

A

23
0-16 conducting
17-19 transitional
20-23 respiratory

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2
Q

What fraction of epithelial cells are goblet cells

A

1/5

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3
Q

What does mucous contain

A

Mucin proteins, proteoglycans and glycosaminoglycans released
from goblet cells and seromucous glands. Give mucus viscoelasticity
• Serum-derive proteins, such as albumin and alpha 1-antitrypsin
also called alpha 1-proteinase inhibitor, an inhibitor of polymorphonuclear neutrophil proteases. Combats microorganism and phagocyte proteases.
• Antiproteases synthesised by epithelial cells r. Combats microorganism and phagocyte proteases.
• Antioxidants from the blood and synthesised by epithelial cells and phagocytes. Combats inhaled oxidants e.g. cigarette smoke, ozone. Also counteracts excessive oxidants released by activated phagocytes.

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4
Q

What happens to goblet cells in smokers

A

Goblet cell number at least doubles (hyperplasia)
• Secretions increase in quantity
• Secretions are thicker

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5
Q

What happens to ciliates cells in smokers

A

Ciliated cells are severely depleted
• Cilia beat asynchronously
• Ciliated cells found in bronchioles (even though reduced in airways)
• Cilia unable to transport thickened mucus - reduced mucus
clearance

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6
Q

What are 2 features of the small airways

A

<2 mm in diameter Not cartilagenous

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7
Q

What are Clara cells

A

Clara Cells = non-ciliated secretory epithelial cells found in large, central, and small airways and bronchi and bronchioles
A major role is XENOBIOTIC METABOLISM
Contain phase 1 and 2 enzymes

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8
Q

Describe type 2 pneumocytes

A

Contain lamellar bodies that store surfactant prior to release onto the air-liquid interface
Synthesise and secrete antiproteases
Positioned in the corners of the alveoli and are embedded in the interstitium with the apical membranes facing the air
Type II cells are very close to capillaries
Type II cells are a precursor for alveolar epithelial type I cells - they divide and differentiate to replace damaged type I cells

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9
Q

Decreased type 1 pneumocytes

A

95% of alveolar surface

Thin and strong

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10
Q

What is the ration of t2:t1

A

2:1

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11
Q

Describe alveolar macrophages

A

Form about 70% of total phagocytic cells in a normal lung
• Macrophages INCREASE 5-10 fold in smokers lungs
Send ‘messages’ to blood/lymphatic system to sequester other inflammatory cells (e.g. neutrophils/lymphocytes) to lungs during infection or as a result of toxicant deposition/inhalation

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12
Q

Polymorphonuclear Neutrophils:

A

found throughout the airways
• Usually only about 5% of lower respiratory tract phagocytes
• INCREASE significantly in number (5-10 fold) and proportionally (up to 30% of
total phagocytes) in smokers and more so during infection

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13
Q

Describe the histopathology of emphysema

A

Infection –> Chronic Damage (T1 cell death) –> Alveolar Fibrosis (repair mechanism)
Increased type II epithelial cells
Increased number of fibroblasts - make a lot of connective tissue (fibrosis)

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14
Q

Summarise the effects of smoking

A

Blocks proliferation and differentiation of Type II cells into Type I cells - and
stimulates apoptosis and necrosis of Type I and Type II cells
Also blocks communication between TII cells and fibroblasts - therefore
blocking repair mechanisms
• INCREASES 10-FOLD NUMBER OF MACROPHAGES AND NEUTROPHILS
Secrete serine proteases (e.g. neutrophil elastase) and metalloproteases (e.g. MMP9), which activate other proteinases and activate cytokines/ chemokines and other pro-inflammatory mediators therefore increasing the number of inflammatory molecules within alveoli —> alveolar inflammation
Also release antimicrobial oxidants - which generate highly reactive peroxides, interacting with proteins and lipids fragmenting connective tissue –> damage
Macrophages also secrete mediators - growth factors + proteases trigger growth and repair by other cells
• Contains Procarcinogens which are activated by phase I enzymes
In normal metabolism, phase II enzymes make these water soluble so that they can be metabolised and excreted
Smoking overloads the pathway, and may inactivate the enzyme, therefore the carcinogen may undergo DNA binding, adduct formation, no repair and mutation

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