02: Lung History & Embryology Flashcards

1
Q

Describe the components of the conducting zone.

A
  • Trachea
  • Bronchi: ciliated & goblet cells, elastic tissue, smooth muscle, glands, cartilage
  • Bronchioles (1 mm): no cartilage or bronchial glands, ciliated lining, no goblet cells, smooth muscle
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2
Q

Basal cell

A

Reserve cell; undifferentiated epithelial cell; divides when injury

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3
Q

Kulchitsky cell

A

Neuroendocrine cells; contain serotonin (5-HT)

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4
Q

Lactoferrin

A

Antioxidant in airway epithelium; bacterio/fungicide

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5
Q

Describe the components of the respiratory zone.

A
  • Terminal bronchiole to respiratory bronchiole
    • Lined by ciliated and clara cells (transitional zone to respiratory bronchiole: all clara cells)
  • Alveolar ducts/sacs
    • Type I & II cells
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6
Q

Clara cells

A

Produce component of surfactant; bronchiolar reserve cell.

Increase in number distally in conducting bronchiole.

P450 (CYP4, CYP1A1): chemical detoxification.

Secrete **CCSP **(antioxidant effect) and surfactant protein B.

Encodes SLPI, a neutrophil protease inhibitor.

Progenitor cell for ciliated bronchiolar cells and other Clara cells.

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7
Q

Type I cells

A

Thin lining cell for gas exchange.

90% of alveolar surface.

Terminally diferentiated.

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8
Q

Type II cells

A

Releases surfactant proteins and lipid.

Regeneration of alveolar epithelial cells (type I & II).

Sodium transport.

Recycle surfactant.

Source of PDGF, TGF B, TGF A, ET-1.

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9
Q

Describe laryngeal development.

A
  • Occurs during week 4
  • Respiratory primordium arises from distal/caudal pharynx: laryngo-tracheal groove.
  • Endodermal derivative of epithelium of larynx, trachea and bronchi.
  • Connective tissue, smooth muscle and cartilage from splanchnic mesenchyme surrounding the foregut.
  • Formation of proximal larynx: cranial tube.
    • Arytenoid swellings grow towards tongue.
    • Airway gets closed off, eventually recanalizes.
  • LT groove evaginates to form LT diverticulum.
    • Becomes invested with splanchnic mesoderm to form lung bud.
    • Maintains a laryngeal inlet.
  • Septum that forms by folds and fusion keeps a septate inlet that becomes the trachea and esophagus.
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10
Q

Laryngeal webs

A

Incomplete recanalization of larynx

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11
Q

Laryngeal atresia

A

Complete upper airway obstruction.

Ascites (hydrops)

Improper lung formation (hypoplasia)

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12
Q

Polyhydramnios

A

Excess intrauterine amniotic fluid 2/2 tracheoesophageal fistula.

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13
Q

Describe early budding/branching.

A
  • By 4 weeks: endodermal buds grow along with splanchnic mesenchyme.
  • By 5 weeks: second degree bronchi, upper middle and lower on right, upper and lower on left.
  • By 6 weeks: tertiary bronchopulmonary segments, 10 on right and 8-9 on left
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14
Q

Describe the stages of lung maturation.

A
  1. **Pseudoglandular **(5-17 wks)
    • No gas exchange zones
    • Lung resembles exocrine gland
  2. **Canalicular **(17-25 wks)
    • Terminal bronchioles enlarge and branch
    • 2-3 respiratory bronchioles then 3-6 alveolar ducts
    • Terminal sacs begin to form
      • Vascularized (caudal slower than cranial)
  3. **Terminal sac/saccular **(25-34 wks)
    • Epithelium thins to become type I like
    • Capillaries grow in
    • Blood air barrier forms: Type I & II cells
      • Surfactant
  4. **Alveolar period **(late fetal - childhood)
    • Surfactant & gas exchange present
    • Pulmonary vs. systemic circulation
    • Alveoli continue maturing from ages 3-8; increase in number from 50 million (birth) to 300 million (age 8; adult number)
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15
Q

Describe the three major congenital malformations of the lungs.

A
  • Cystic adenomatoid malformations: maturation arrest in lung segments
  • Azygos lobe: superior apical bronchus grows medially instead of laterally; vein at bottom of superior lobe fissure
  • Sequestration: accessory piece of lung that becomes disconnected from tracheobronchial tree and parasitizes systemic circulation from diaphragm
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16
Q

Describe breathing exercise in the development of the lungs.

A
  • Begins pre-natally, allows branching to continue
    • Fluid expelled from lungs into capillaries and lymphatics at birth by vaginal pressure
  • Fluid needed for proper lung development
    • Insufficient fluid –> decreased lung development
    • Insufficient breathing movements –> decreased neurological lung development
17
Q

Lung hypoplasia

A

Diminished lung development due to:

  • Oligohydramnios: insufficient amniotic fluid
  • Compression:
    • Congenital diaphragmatic hernia: intestinal contents compress left hemithorax
    • **Intrathoracic fluid **or thoracic wall abnormality
18
Q

Respiratory Distress Syndrome (RDS)

A
  • Low surfactant 2/2 pre-maturity or surfactant protein deficiency (rare)
  • Leads to alveolar collapse upon expiration, difficulty re-inflating
  • Alveolus damage –> cellular injury and exudation of proteins known as hyaline membranes
    • Continued injury can lead to bronchopulmonary dysplasia
  • Administer steroids (accelerate lung development and surfactant production) and surfactant.