HE 20 & 21 Respiratory System Flashcards

2
Q

Trends of Tracheobronchial Tree

A

Epithelium: pseudostrat column to simple cuboidal-less cleaning cellsWalls: less layers-no more mucosa or cartilageStructure: (cartilage) (sm + cart) (sm + EF)

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3
Q

trachealis muscle

A

smooth muscle bundle posterior to C rings of cartilage in trachea

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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

poorly stain
endocrine cell
enteroendocrine or ENES cell

trachea and bronchi

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5
Q

key features of Trachea

A

cartilage ringsthickest epitheliumTrachealis MuscleNo muscularishigh in mucus from two places-mucosal epithelium-submucosal glandsepithelium/LP/submucosa

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6
Q

Four types of cells in tracheal epithelium

A

goblet: mucus in lumenciliated: move mucusbasal cell: regenerates epitheliumkulchitsky cell: signals and regulates, basally secretes serotonin and peptide hormone, affects goblet, ciliated cells

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7
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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8
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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9
Q

Bronchioles and dysfunction

A

NO cartilagethick muscularis: throws epithelium into folds-NO MUCUS PRODUCTION-simple columnar or cuboidal -ciliated cells present but gradually lostASTHMA: inflammation of bronchi and bronchioles-mast cells degranulation cause sudden constrictions of muscularis, narrowing lumen

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10
Q

epithelial cells of bronchioles

A

ciliated cells present but gradually lostsimple columnar or cuboidal-clara cellsL bulge into lumen: secrete surfactant keeping lumen openterminal bronchiole: mostly clara, few ciliated, no alveoli buds

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11
Q

components and significance of bronchiolar unit

A

respiratory bronchiolealveolialveolar ductalveolar sacmost gas exchange here-appear lacey with islands (resp bronch) in histo

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12
Q

resp bronchiole

A

alveoli budscuboidal clara cellsbronkens islands of smooth muscle(trunk part: beginning of gas exchange)

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13
Q

alveolar duct:

A

leads to alveolar saclacks smooth muscle islandswalls composed of alveolihas sacs as base

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14
Q

alveolus

A

small air capsulsurrounded by thin continuous extremely tight capillaries -Type I and Type II pneumocytes-alveolar macrophagesalveolar wall: simple epithelium +BL

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15
Q

Type I pneumocyte

A

flat wide cell95% of SA of wallcannot regeneratepart of blood/air barrierlook for flat cell with nucleus that bulges into space

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16
Q

type II pneumocyte

A

bubbly look from lamellar bodies (secretory vescicles with surfactant)-different surfactant than claramore abundant but only 5% of surface area of wall. CAPABLE OF REGENERATION

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17
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

18
Q

dust cells

A

alveolar macrophages, phagocytose particulate matter in lumen and septum

19
Q

emphysema

A

too many particulatesdust cells become overactivedust cells release enzymes that break down alveolar septa -less surface area, less gas exchange, less recoil to expire air

20
Q

week 3, 4, 5 conceptualization

A

3: lateral plate mesoderm splits into parietal and visceral4. 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&5canals 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

21
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

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

ESOPHAGUS is the one screwed up

23
Q

lung embryonic origin

A

endoderm: epithelium of resp systemvisceral mesodermL lamina propria, muscularis, submucosa, cartilage, adventitia, visceral pleura

24
Q

week five to early post natal lung development

A

primary-secondary-tertiarybronchopulmonary segmentation-continues after birth (six more divisions)

25
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)

26
Q

pericardioperitoneal canals

A

lateral body folding (all body folding) leaves spaces on either sides of the gut tube, later a place for lungs to grow

27
Q

pleruopericardial membranes/folds

A

one pair of folds from lung budding causing them to divide the lungs and the heart, FUSION at root of lung, divides lungs into two different cavities and heart into a cavity

28
Q

pleuroperitineal membranes/folds

A

second pair of folds from lung budding causes them to move down and attach to the septum transversum (actually two separate ones with a loop division in middle)

-mesoderm plate started from caphalocaudal body folding