1. Hal Hawkins, Ph.D.,M.D. Fundamentals of Inflammation Course, BBSC 6210 June 25, 2012

2. Vasodilation and vascular leakage Cellular: recruitment activation functions tissue Injury

10. » Tumor – edema due to plasma leakage » Rubor – dilation of arterioles and engorgement of microvasculature » Calor – increased local temperature » Dolor –probably due to stretching and prostaglandins

15. MARGINATION ADHERENCE EMIGRATION AND CHEMOTAXIS

17. The tongue of the frog provides an opportunity to see the microcirculation and the movements of neutrophils.

18. “With the slowing of blood flow in the dilated venules leukocytes appear in the marginal stream and tend to stick to the vessel walls. At first the leukocytes stick momentarily and are then displaced to be washed away by the blood stream.“

19. “As they begin to adhere more closely some are pushed slowly along by the blood stream, becoming flattened and elongated in the direction of the flow so that they have the appearance of blobs of jelly being pushed along over a sticky surface.”

20. “Gradually some of the cells adhere more firmly until even a relatively swift stream of plasma and red corpuscles cannot dislodge them. With an adequate injury some of the leukocytes sticking to the wall begin to make their way through it by active movements, taking 2 to 12 minutes to do so. “

27. Armond Goldman’s discovery of neutrophil integrins

29. » http://www.youtube.com/watch?v=9wxK6oLA5 oc http://www.youtube.com/watch?v=9wxK6oLA5 oc

30. » http://www.youtube.com/watch?v=DMvixApKz Ks http://www.youtube.com/watch?v=DMvixApKz Ks

32. (from Marchesi and Florey)

33. » Receptors (complement, IgG, etc.) » PAF (platelet activating factor) » Phospholipase  Inositol triphosphate  Ca++ release Diacylglycerol  Protein kinase C

36. http://www.youtube.com/watch?v=ZUUfdP87Ssg

37. » Complement fragment C5a » Bacterial formylated peptides » Arachidonic acid products, e.g. Leukotriene B4 » Cytokines called chemokines, e.g. IL-8

43. » PHAGOCYTOSIS » FUSION OF GRANULES » BACTERIAL KILLING

47. » O 2 -, superoxide » H 2 O 2, peroxide » HOCl, hypochlorous acid  » OH, hydroxyl radical » Acid hydrolases (enzymes) » Bactericidal proteins, defensins, lactoferrin, lysozyme

48. Pneumonia

49. »Plasma proteases, e.g. complement »Vasoactive amines, e.g. histamine »Platelet-activating factor PAF »Arachidonic acid metabolites, e.g. prostaglandin E3 »Reactive oxygen and nitrogen species »Cytokines and chemokines, e.g. IL-8 »Neuropeptides and endothelin

51. »Products of arachidonic acid metabolism »Potent vasodilators/vasoconstrictors »Cyclo-oxygenase (COX), needed for prostaglandin synthesis, is inhibited by aspirin and selective COX2 inhibitors including the notorious Vioxx »Important in fever and pain »Lipoxygenase leads to leukotrienes, proinflammatory lipids active in asthma

52. » O 2 -, superoxide » H 2 O 2, peroxide » HOCl, hypochlorous acid » OH, hydroxyl radical » ONOO -, peroxynitrite (all reactive oxygen and nitrogen species) »Lysosomal neutral hydrolases

53. »Follows emigration and phagocytosis »Minimizes tissue injury

54. » DELAY: ˃GM-CSF G-CSF ˃LPS, IL-1, IL-2 ˃IFN-gamma » STIMULATE: ˃IL-6 ˃Phagocytosis ˃Oxidative burst

55. » Cellular contents may not be released » Clearance by macrophages stimulates activation of macrophages to secrete factors favoring wound healing Neutrophil apoptosis is the key to prevention of tissue injury.

56. Recognition of Pathogen Activated Molecular Pathways (PAMPs) including Toll Like Receptors (TLRs) and Damage Activated Molecular Pathways (DAMPs) (together sometimes called Alarmins). TLRs stimulate release of multiple pro-inflammatory peptides. DAMPs lead to assembly of inflammasomes, activation of caspase-1, and production of IL-1beta.