HE 20 21: Lung Flashcards

1
Q

Trends of Tracheobronchial Tree

A

Epithelium: pseudostrat column to simple cuboidal
-less cleaning cells

Walls: less layers
-no more mucosa or cartilage

Structure: (cartilage) (sm + cart) (sm + EF)

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2
Q

trachealis muscle

A

smooth muscle bundle posterior to C rings of cartilage in trachea

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3
Q

key features of Trachea

A

cartilage rings

thickest epithelium

Trachealis Muscle

No muscularis

high in mucus from two places

  • mucosal epithelium
  • submucosal glands

epithelium/LP/submucosa

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4
Q

kulchitsky cell

A

signals and regulates

  • secretes basally serotonin and peptide hormone
  • may affect nerve endings, goblet, & ciliated cells
  • regulated secretion
  • related to enteroendocrine of the gut
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5
Q

Four types of cells in tracheal epithelium

A

goblet: mucus in lumen
ciliated: move mucus

basal cell: regenerates epithelium

kulchitsky cell: signals and regulates, basally secretes serotonin and peptide hormone, affects goblet, ciliated cells

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6
Q

mucocilliary escalator and dysfunction

A

combination of ciliated cells that sweep mucosa out of the airway (mucosa contains particles trapped)

Cystic Fibrosis caused by mutation of Cl- channel in respiratory epithelium. Ion gradient becomes unbalances and luminal mucus dehydrates. This thick mucus impedes mucocilliary escalator, making this area prone to infection

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7
Q

Intrapulmonary Bronchi Characteristics

A

Lobar and segmental
-hyaline cartilage plates

-continuous muscularis (corresponds to increasing role of bronchioconstriction)

segmental bronchus >bronchiole> lobule

lobule: independent blood drainage)

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8
Q

Bronchioles and dysfunction

A

NO cartilage

thick muscularis: throws epithelium into folds

  • NO MUCUS PRODUCTION
  • simple columnar or cuboidal
  • ciliated cells present but gradually lost

ASTHMA: inflammation of bronchi and bronchioles
-mast cells degranulation cause sudden constrictions of muscularis, narrowing lumen

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9
Q

epithelial cells of bronchioles

A

ciliated cells present but gradually lost

simple columnar or cuboidal

-clara cellsL bulge into lumen: secrete surfactant keeping lumen open

terminal bronchiole: mostly clara, few ciliated, no alveoli buds

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10
Q

components and significance of bronchiolar unit

A

respiratory bronchiole
alveoli
alveolar duct
alveolar sac

most gas exchange here
-appear lacey with islands (resp bronch) in histo

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11
Q

resp bronchiole

A

alveoli buds

cuboidal clara cells

bronkens islands of smooth muscle

(trunk part: beginning of gas exchange)

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12
Q

alveolar duct:

A

leads to alveolar sac

lacks smooth muscle islands

walls composed of alveoli

has sacs as base

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13
Q

alveolus

A

small air capsul

surrounded by thin continuous extremely tight capillaries

  • Type I and Type II pneumocytes
  • alveolar macrophages

alveolar wall: simple epithelium +BL

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14
Q

Type I pneumocyte

A

flat wide cell

95% of SA of wall
cannot regenerate

part of blood/air barrier

look for flat cell with nucleus that bulges into space

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15
Q

type II pneumocyte

A

bubbly look from lamellar bodies (secretory vescicles with surfactant)
-different surfactant than clara

more abundant but only 5% of surface area of wall.

CAPABLE OF REGENERATION

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16
Q

blood/air barrier

A

thin: gas exchange- continuous with blood vessels along alveolar septum (two alveolar walls)

thick areas: contain fibroblasts/elastic fibers, macrophages- serve to support

17
Q

dust cells

A

alveolar macrophages, phagocytose particulate matter in lumen and septum

18
Q

emphysema

A

too many particulates

dust cells become overactive

dust cells release enzymes that break down alveolar septa

-less surface area, less gas exchange, less recoil to expire air

19
Q

week 3, 4, 5 conceptualization

A

3: lateral plate mesoderm splits into parietal and visceral

  1. lateral body folding
    -creates gut tube in embryonic cavity (coelom)
    cephalocaudal folding: pushes thick plate (septum transversum) between thoracic cavity and yolk sac
    -creates large openings (pericardioperitoneal canals)

4&5
canals compressed by lung buds to make two pairs of folds
-pleurocardial membranes (fuse witheachother and root of lunch to form pericardial and two pleural cavities

-lung budding also causes pleuroperitoneal folds to extend btween thor and ab. cavities creating thoracic diaphragm

20
Q

congenital diaphragmatic hernia

A

incomplete closure of one or both pleuroperitoneal membranes.

abdominal gut tube herniates into the pleural cavity compressing the lungs and prevents full development in infants

21
Q

lung embryonic origin

A

endoderm: epithelium of resp system

visceral mesodermL lamina propria, muscularis, submucosa, cartilage, adventitia, visceral pleura

22
Q

Respiratory Diverticulum and dysfunction

A

buds off ventral aspect of foregut: is the beginning of trachea and esophagus

-driven by Retinoic acid expression of adjacent visceral mesoderm driving TBX4

Esophageal atresia/tracheoesophageal fistulae- incorrect partitioning of the trachea and esophagus

  • choking and regurg of food, pneumonitis, polyhydramnios
  • most common (90)-atretic esophagus
23
Q

week five to early post natal lung development

A

primary-secondary-tertiary

bronchopulmonary segmentation

-continues after birth (six more divisions)

24
Q

month 7 to prenatal (10yrs)

A

at seven months, TRUE barrier for gas exchange is formed. continue to develop to 10 yrs.

see figure of capillaries micrating to alveoli (month 6)