PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 68 | 05 |

Tytuł artykułu

Immunobiologia komórek NK

Warianty tytułu

EN
Immunobiology of NK cells

Języki publikacji

PL

Abstrakty

EN
NK (natural killer) cells are lymphoid, often granular, cells that are an important component of natural immunity, along with the complement system and phagocytic activity. NK cells are defined as cells of the innate immune response. Recent studies, however, demonstrate that specific subsets of mouse NK cells can develop specific immunological “memory” to a variety of antigens. NK cells do not require prior contact with foreign (i.e. viral or tumor) antigens and are not MHC-restricted. NK cells are involved in antibody- -dependent cell-mediated cytotoxicity (ADCC) and are thus able to destroy target cells coated with antibodies. NK cells express strong cytotoxicity against neoplastic and virus-infected cells after the activation of the perforin/granzyme system. They express stimulatory and inhibitory receptors on cell surface that recognize self-MHC proteins and regulate their activation. Mice NK cells express a large number of receptors, such as Ly49 receptors, which can inhibit the activity of MHC class I molecules. This short review shows an important role of NK cells as the effector arms of the immune system.

Wydawca

-

Rocznik

Tom

68

Numer

05

Opis fizyczny

s.274-279,tab.,bibliogr.

Twórcy

autor
  • Zakład Immunologii, Katedra Nauk Przedklinicznych, Wydział Medycyny Weterynaryjnej, Szkoła Główna Gospodarstwa Wiejskiego, ul.Ciszewskiego 8, 02-786 Warszawa
autor
autor

Bibliografia

  • 1. Antoniou C. E., Andrews D. M., Degli-Esposti M. A.: Natural killer cells in viral infection: more than just killers. Immunol. Rev. 2006, 214, 239-250.
  • 2. Arase H., Lanier L. L.: Virus-driven evolution of natural killer cell receptors. Microb. Infect. 2002, 15, 1505-1512.
  • 3. Billadeau D. D., Leibson P. J.: ITAMs versus ITIMs: strikin a balance during cell regulation. J. Clin. Invest. 2002, 109, 161-168.
  • 4. Björkström N. K., Ljunggren H. G., Sandberg J. K.: CD56 negative NK cells: origin, function, and role in chronic viral disease. Trends Immunol. 2010, 31, 401-406.
  • 5. Chiesa S., Tomasello E., Vivier E., Vely F.: Coordination of activating and inhibitory signals in natural killer cells. Mol. Immunol. 2005, 42, 477-484.
  • 6. Chlewicki L. K., Velikovsky C. J., Balakrishnan V., Mariuzza R. A., Kumar V.: Molecular basis of the dual functions of 2B4 (CD244). J. Immunol. 2008, 180, 8159-8167.
  • 7. Dokun A. O., Kim S., Smith H. R., Kang H. S., Chu D. T., Yokoyama W. M.: Specific and nonspecific NK cell activation during virus infection. Nat. Immunol. 2001, 2, 951-956.
  • 8. Eriksson M., Leitz G., Fallman E., Axner O., Ryan J. C., Nakamura M. C., Sentman C. L.: Inhibitory receptors alter natural killer cell interactions with target cells yet allow simultaneous killing of susceptible targets. J. Exp. Med. 1999, 190, 1005-1012.
  • 9. Fahlen L., Lendahl U., Sentman C. L.: MHC class I-LY49 interactions ahape the LY49 repertoire on murine NK cells. J. Immunol. 2001, 166, 6585-5492.
  • 10. Farag S. S., Fehniger T. A., Ruggeri L., Velardi A., Caligiuri M. A.: Natural killer cell receptors: new biology and insights into the graft-versus-leukemia effect. Blood 2002, 100, 1935-1947.
  • 11. Fodil-Cornu N., Loredo-Osti J. C., Vidal S. M.: NK cell receptor/H2-Dk - dependent host resistance to viral infection is quantitatively modulated by H2q inhibitory signals. PLoS Genet. 2011, 7, e1001368.
  • 12. García-Sastre A., Biron C. A.: Type 1 interferons and the virus-host relationship: a lesson in detente. Science 2006, 312, 879-882.
  • 13. Gillard G. O., Bivas-Benita M., Hovav A.-H., Grandpre L. E., Panas M. W., Seaman M. S., Haynes B. F., Letvin N. L.: Thy1⁺ NK cells from vaccinia virus-primed mice confer protection against vaccinia virus challenge in the absence of adaptive lymphocytes. PloS Pathog. 2011, 7, e1002141.
  • 14. Gonzalez V. D., Falconer K., Björkström N. K., Blom K. G., Weiland O., Hans-Ljunggren G., Alaeus A., Sandberg J. K.: Expansion of functionally skewed CD56-negative NK cells in chronic hepatitis C virus infection: correlation with outcome of pegylated IFN-á and ribavirin treatment. J. Immunol. 2009, 183, 6612-6618.
  • 15. Held W., Coudert J. D., Zimmer J.: The NK cell receptor repertoire formation, adaptation and exploitation. Curr. Opin. Immunol. 2003, 15, 233-237.
  • 16. Iannello A., Debbeche O., Samarani S., Ahmad A.: Antiviral NK cell responses in HIV infection: II. viral strategies for evasion and lessons for immunotherapy and vaccination. J. Leukoc. Biol. 2008, 84, 27-49.
  • 17. Kärre K.: Natural killer cell recognition of missing self. Nat. Immunol. 2008, 9, 477-480.
  • 18. Khakoo S. I., Brooks C. R.: MHC class I receptors on natural killer cells: on with the old and in with the new. Clin. Sci. (Lond). 2003, 105, 127-140.
  • 19. Kubota A., Kubota S., Lohwasser S., Mager D. L., Takei F.: Diversity of NK cell receptor repertoire in adult and neonatal mice. J. Immunol. 1999, 163, 212-216.
  • 20. Lanier L. L.: Evolutionary struggles between NK cells and viruses. Nat. Rev. Immunol. 2008, 8, 259-268.
  • 21. Lanier L. L.: Natural killer cell receptor signaling. Curr. Opin. Immunol. 2003, 15, 308-314.
  • 22. Lanier L. L.: NK cell recognition. Annu. Rev. Immunol. 2005, 23, 225-274.
  • 23. Lanier L. L.: Turning on natural killer cells. J. Exp. Med. 2000, 17, 1259-1262.
  • 24. Mack E. A., Kallal L. E., Demers D. A., Biron C. A.: Type 1 interferon induction of natural killer cell gamma interferon production for defense during lymphocytic choriomeningitis virus infection. MBio. 2011, 2, e00169-11.
  • 25. Makrigiannis A. P., Anderson S. K.: The murine LY49 family: form and function. Arch. Immunol. Ther. Exp. 2001, 49, 47-50.
  • 26. Martin-Fontecha A., Carbone E.: The social life of NK cells. Arch. Immunol. Ther. Exp. 2001, 49 Suppl 1:S33-S39.
  • 27. Mian M. F., Lauzon N. M., Stämpi M. R., Mossman K. L., Ashkar A. A.: Impairment of human NK cell cytotoxic activity and cytokine release by cigarette smoke. J. Leukoc. Biol. 2008, 83, 774-784.
  • 28. Miller-Kittrell M., Sparer T. E.: Feeling manipulated: cytomegalovirus immune manipulation. Virol. J. 2009, 6, 4.
  • 29. Mselle T. F., Meadows S. K., Eriksson M., Smith J. M., Shen L., Wira C. R., Sentman C. L.: Unique characteristics of NK cells throughout the human female reproductive tract. Clin. Immunol. 2007, 124, 69-76.
  • 30. Nakamura M. C., Niemi E. C., Fisher M. J., Shultz L. D., Seaman W. E., Ryan J. C.: Mouse LY-49A interrupts early signaling events in natural killer cell cytotoxicity and functionally associates with the SHP-1 tyrosine phosphatase. J. Exp. Med. 1997, 185, 673-684.
  • 31. Orange J. S., Fassett M. S., Koopman L. A., Boyson J. E., Strominger J. L.: Viral evasion of natural killer cells. Nat. Immunol. 2002, 3, 1006-1012.
  • 32. Ortaldo J. R., Bere E. W., Hodge D., Young H. A.: Activating LY-49 NK receptors: central role in cytokine and chemokine production. J. Immunol. 2001, 166, 4994-4999.
  • 33. Ortaldo J. R., Young H. A.: Mouse LY49 NK receptors: balancing activation and inhibition. Mol. Immunol. 2005, 42, 445-450.
  • 34. Proteau M. F., Rousselle E., Makrigiannis A. P.: Mapping of the BALB/C LY49 cluster defines a minimal natural killer cell receptor gene repertoire. Genomics 2004, 84, 669-677.
  • 35. Pyzik M., Gendron-Pontbriand E.-M., Vidal S. M.: The impact of Ly49-NK cell-dependent recognition of MCMV infection on innate and adaptive immune responses. J. Biomed. Biotechnol. 2011, 641702.
  • 36. Ravetch J. V., Lanier L. L.: Immune inhibitory receptors. Science 2000, 290, 84-89.
  • 37. Russell J. H., Ley T. J.: Lymphocyte-mediated cytotoxicity. Annu. Rev. Immunol. 2002, 20, 323-370.
  • 38. Sène D., Levasseur F., Abel M., Lambert M., Camous X., Hernandez C., Pène V., Rosenberg A. R., Jouvin-Marche E., Marche P. N., Cacoub P., Caillat-Zucman S.: Hepatitis C virus (HCV) evades NKG2D-dependent NK cell responses through NS5A-mediated imbalance of inflammatory cytokines. PLoS Pathog. 2010, 6, e1001184.
  • 39. Silver E. T., Gong D. E., Chang C. S., Amrani A., Santamaria P., Kane K. P.: LY-49P activates NK-mediated lysis by recognizing H-2DD. J. Immunol. 2000, 165, 771-781.
  • 40. Smith H. R., Chuang H. H., Wang L. L., Salcedo M., Heusel J. W., Yokoyama W. M.: Nonstochastic coexpression of activation receptors on murine natural killer cells. J. Exp. Med. 2000, 191, 1341-1354.
  • 41. Smith K. M., Wu J., Bakker A. B., Phillips J. H., Lanier L. L.: LY-49D and LY-49H associate with mouse DAP12 and form activating receptors. J. Immunol. 1998, 161, 7-10.
  • 42. Sun J. C., Beilke J. N., Lanier L. L.: Adaptive immune features of natural killer cells. Nature 2009, 457, 557-561.
  • 43. Tay C. H., Yu L. Y., Kumar V., Mason L., Ortaldo J. R., Welsh R. M.: The role of LY49 NK cell subsets in the regulation of murine cytomegalovirus infections. J. Immunol. 1999, 162, 718-726.
  • 44. Trapani J. A., Smyth M. J.: Functional significance of the perforin/granzyme cell deth pathway. Nat. Rev. Immunol. 2002, 2, 735-747.
  • 45. Voigt S., Mesci A., Ettinger J., Fine J. H., Chen P., Chou W., Carlyle J. R.: Cytomegalovirus evasion of innate immunity by subversion of the NKR-P1B:Clr-b missing-self axis. Immunity 2007, 26, 617-627.
  • 46. Voigt V., Forbes C. A., Tonkin J. N., Degli-Esposti M. A., Smith H. R., Yokoyama W. M., Scalzo A. A.: Murine cytomegalovirus M157 mutation and variation leads to immune evasion of natural killer cells. PNAS USA 2003, 100, 13483-13488.
  • 47. Webb J. R., Lee S. H., Vidal S. M.: Genetic control of innate immune responses against cytomegalovirus: MCMV meets its match. Genes Immun. 2002, 3, 250-262.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-ab74c1d6-a36f-4746-a7f9-92ba05148b4b
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.