Pulmonary defense mechanisms + non-resp. functions of lungs Flashcards
What are the 6 primary defense mechanisms of the upper airways and bronchi?
- –Anatomic barriers
- –Cough
- –Mucociliary apparatus
- –Airway epithelium
- –Secretory IgA
- –Dendritic cells, lymphocytes, neutrophils
What are the 4 primary host defense mechanisms of the alveolar spaces?
- –Alveolar macrophages
- –Immunoglobulins, opsonins, and surfactants
- –Lymphocyte-mediated immunity
- –Neutrophils and eosinophils
Why is it important that defenses of the lung limit inflammation?
Causes probrems with gas exchange
What immune cells are present in the lung airways?
Alveolar macros
resp. dendritic cells
virus specific B cells
Memory T cell
What immune cells are found in the lung parenchyma?
Memory T cell
Resp. Dedritic cells
Immune cells in lung draining lymph node?
Memory T cells
Lymph node dendritic cells
naive T cell
Virus specific B cell
•A cough can be triggered by chemicals, mechanical stimulation, inflammation, or be voluntary. Describe the sequence of events in the cough reflex
- Deep inspiration
- Trapping of air by shutting off its exit (glottis in the case of cough)
- Initiation of expiratory effort, raising the intrathoracic pressure
- Build up of pressure
- Sudden release of the trapped air at a high pressure
Airway epithelium has is own complement of defensive mechanisms. Describe them
•Barrier function
•Defense function
–Release of bacteriostatic molecules
–Regulation of the immune response- contain receptors and
produce cytokines
•transport the IgA secreted by plasma cells
What do the bacteriostatic molecules released by airway epithelium do?
Prevent bacterial growth
BALT stands for?
Bronchial associated lymphoid tissue
What defense molecules are contained in mucus?
•IgA, lysozyme, lactoferrin and peroxidases
What particle size range does mucus deal with?
•Particles larger than 2-3 µm and smaller than 10 µm are deposited on the mucus of the upper airways
What are three examples of disease states that alter the mucociliary clearance response?
Asthma
Chronic bronchitis
cystic fibrosis
Mucins can be either…
secreted or attached
What does CF arise from?
•CF arises from a mutation in the gene cystic fibrosis transmembrane conductance regulator (CFTR)