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Ch. 12 Cytokines- essential for cell-to-cell communication

Ch. 12 Cytokines- essential for cell-to-cell communication. Properties of cytokines Receptors Agonists and antagonists Secreting cells Cytokine-related diseases Therapeutics. p. 303. p. 304. Activity was noted long before cytokines could be isolated Present in very small amounts

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Ch. 12 Cytokines- essential for cell-to-cell communication

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  1. Ch. 12 Cytokines- essential for cell-to-cell communication Properties of cytokines Receptors Agonists and antagonists Secreting cells Cytokine-related diseases Therapeutics

  2. p. 303

  3. p. 304

  4. Activity was noted long before cytokines could be isolated Present in very small amounts Hard to characterize Process was helped along by: gene cloning technology cytokine-dependent cell lines monoclonal antibodies

  5. General structure of cytokines Small (<30 kD) Proteins or glycoproteins Are assigned to families based on structure; four families identified so far

  6. p. 305

  7. p. 305

  8. Summary of (some) functions: • Regulate hematopoiesis • Colony-stimulating factors • IL-3 can cause many types of cells to divide • IL-7 differentiation into pre-B and pre-T cells 2. Innate immune responses IL-1, IL-6, TNF-, INF- and INF- produced mostly by macrophages and neutrophils fever, acute-phase response, recruit leukocytes to site of damage

  9. 3. Inflammation all of the above (part 2) IFN-- activates macrophages TGF-- terminates inflammatory response 4. Specific immune responses IL-2 T cell growth factor IL-4 T and B cells IL-5 and IL-6 B cell proliferation and differentiation 5. Chemokines: attract leukocytes IL-8 RANTES (see Ch. 12 for more extensive list)

  10. p. 307

  11. Be advised: Most of these activities were described in non-physiological conditions and at non-physiological concentrations No cytokine acts alone Many act in cascades; not always clear which is the real effector Many are pleiotropic How is this activity regulated?

  12. Cytokine receptors Cytokines must bind to specific receptors to activate cells A particular type of receptor may be expressed on many cells Families of receptors:

  13. Immunoglobulin Class I cytokine receptor Class II TNF receptor Chemokine

  14. These vary in: Structure Distribution Can be sorted into categories because they have characteristic structures Many cytokines involved in immune and hematopoietic function are class I

  15. Class I and class II receptors tend to have multiple subunits: one involved in binding and one in signal transduction Signal transduction subunit may be common to many

  16. p. 309

  17. p. 311

  18. p. 312

  19. Cytokine antagonists- two mechanisms Inhibitor binds to receptor and blocks it (e.g., IL-1Ra) Soluble receptors bind to cytokines so they can’t bind to membrane-bound receptors (soluble IL-2 receptor among many others; released in chronic T-cell activation)

  20. p. 314

  21. TH1 and TH2 subsets secrete different cytokines TH1- cell-mediated functions; inflammation TH2- humoral immunity

  22. p. 315

  23. TH1 and TH2 subsets regulate each other

  24. p. 316

  25. p. 317

  26. Cytokine-related diseases Bacterial septic shock endotoxins (cell walls) stimulate production of IL-1 and TNF- Cancers of lymphoid system- overproduction of cytokines such as IL-6 (B-cell) or IL-5 (Hodgkin’s disease) or IL-2 (adult T-cell leukemia) Chagas’ disease (parasitic)- suppression of -subunit of IL-2 receptor

  27. Cytokine therapies Interferons IFN-- certain types of tumors IFN-- multiple sclerosis these are antiviral IFN-- chronic granulomatous disease IL-2- certain types of cancer infusion LAK (lymphokine-activated killer) cells TILs (tumor-infiltrating lymphocytes) GM-CSF- immune deficiencies

  28. TNF (tumor necrosis factors) TNF- and  In some cases inhibit proliferation of tumor cells but not normal cells May damage vascular endothelial cells in tumors, thus inhibiting blood supply to the tumor

  29. p. 320

  30. Toxin-conjugated cytokines: kill TH cells and prevent graft rejection Problems: rapidly cleared from system can be very toxic doses are hard to control Possible solutions: ex vivo cell culture conjugate cytokines to other molecules modify cytokines? p. 323: Cytokine therapies in clinical use

  31. p. 324

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