Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-04.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
Natural killer cell activity in mice infected with free-living amoeba with reference to their pathogenicity
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 31(3):1993 > Article

Original Article
Korean J Parasitol. 1993 Sep;31(3):239-248. Korean.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1993.31.3.239
Copyright © 1993 by The Korean Society for Parasitology
Natural killer cell activity in mice infected with free-living amoeba with reference to their pathogenicity
K H Kim,C O Shin and K Im*
Department of Parasitology and Institute of Tropical Medicine, College of Medicine, Yonsei University, Seoul 120-752, Korea.
Received May 29, 1993; Accepted July 31, 1993.

Abstract

The purpose of this observation was to investigate the natural killer cell activities in mice infected with pathogenic free-living amoeba, Naegleria fowleri and Acanthamoeba culbertsoni according to the infection doses, and infected with non-pathogenic free-living amoeba, Naegleria gruberi. The natural killer cell activity was examined by means of target binding capacity, active NK cell and maximum recycling capacity of the mice after inoculating free-living amoebae with low and high doses. The mice infected with 1,103, 1,105 A. culbertsoni trophozoites showed mortality rates of 6.9% and 65.5%, respectively. The mice infected with 1,104, 1,105 N. fowleri trophozoites showed mortality rates of 5.9% and 72.2%, respectively. The NK cell activities in all experimental groups increased significantly on day 1 after infection as compared with control group, and then remarkably declined thereafter, there was no difference of the cytotoxic activity of the NK cells in mice among inoculation doses of pathogenic free-living amoebae. The target binding capacities of NK cells and percentages of activated NK cells in mice infected with pathogenic free-living amoebae were significantly increased a day after infection, as compared with control group. There was no difference of the maximal recycling capacities of NK cells in all experimental groups as compared with control group. There was significant difference in the cytotoxic activity and single cell cytotoxicity of NK cells between the experimental groups infected with pathogenic free-living amoebae and that infected with non-pathogenic free-living amoebae.

Figures


Fig. 1
An example of figures showing Vmax and Km values. (A) Data from Table 1 are used to examplify the calculation of Vmax. Initial number of target cells (T) is plotted against number of dead target cells (V) at the end of the test. The points fit well to the theoretical Michaelis-Menten saturation curve. (B) A Line Weaver-Burk plot is used to calculate Vmax and km. 1/T = X plotted against 1/V = Y. Data are taken from Table 1 and Fig. 1 (A). Regression analysis is used to obtain a straight line (r = 0.92). Vmax equals the reciprocal of the Y intercept and km equals the negative reciprocal of the X intercept.


Fig. 2
Natural killer cell cytotoxic activity against YAC-1 target cells in mice infected with free-living amoebae.***p<0.05 versus control


Fig. 3
Target binding capacity by single cell cytotoxicity in mice infected with free-lining amoeba.***p < 0.05 versus control


Fig. 4
Fraction of dead conjugates by single cell cytotoxicity in mice infected with free-living amoeba.***p < 0.05 versus control


Fig. 5
Active NK cells by single cell cytotoxicity in mice infected with free-living amoeba.***p < 0.05 versus control


Fig. 6
Values of Vmax of natural killer cell in mice infected with free-living amoeba.***p < 0.05 versus control


Fig. 7
Maximal recycling capacity of natural killer cells in mice infected with free-living amoeba.

Tables


Table 1
An experiment showing data used for calculation of Vmax and Kim*


Table 2
Cumulative number of death in mice inculated intranasally with the free-living amoebae


Table 3
Correlation matrix between NK activity, TBC Active NK cells, Vmax and MRC infected with N. fowleri 1 × 105 trophozoites

References
1. Kim MJ, Shin CO, Im KI. [Cell-mediated immunity in mice infected with Acanthamoeba culbertsoni]. Korean J Parasitol 1990;28(3):143–154.
 
2. Lee KR, Shin CO, Im K. [Natural killer cell activity in Naegleria fowleri infected mice]. Korean J Parasitol 1991;29(3):267–277.
 
3. Hyun DK, Shin CO, Im K. [Natural killer cell activity in mice infected with Acanthamoeba culbertsoni]. Korean J Parasitol 1992;30(2):101–112.
 
4. Bradley TP, Bonavida B. Mechanism of cell-mediated cytotoxicity at the single cell level. IV. Natural killing and antibody-dependent cellular cytotoxicity can be mediated by the same human effector cell as determined by the two-target conjugate assay. J Immunol 1982;129(5):2260–2265.
 
5. Cikes M, Friberg S Jr, Klein G. Progressive loss of H-2 antigens with concomitant increase of cell-surface antigen(s) determined by Moloney leukemia virus in cultured murine lymphomas. J Natl Cancer Inst 1973;50(2):347–362.
 
6. Clark IA, et al. Nature 1974;252:318–325.
7. Derrick EH. Trans Roy Soc Med Hyg 1948;42:191–198.
 
8. Duke RC, Chervenak R, Cohen JJ. Endogenous endonuclease-induced DNA fragmentation: an early event in cell-mediated cytolysis. Proc Natl Acad Sci U S A 1983;80(20):6361–6365.
  
9. Grimm EA, Bonavida B. Studies of the induction and expression of T cell mediated immunity. VI. Heterogeneity of lytic efficiency exhibited by isolated cytotoxic T lymphocytes prepared from highly enriched populations of effector-target conjugates. J Immunol 1977;119(3):1041–1047.
 
10. Hatcher FM, Kuhn RE. Destruction of Trypanosoma cruzi by Natural killer cells. Science 1982;218(4569):295–296.
  
11. Hatcher FM, Kuhn RE. Spontaneous lytic activity against allogeneic tumor cells and depression of specific cytotoxic responses in mice infected with Trypanosoma cruzi. J Immunol 1981;126(6):2436–2442.
 
12. Hatcher FM, Kuhn RE, Cerrone MC, Burton RC. Increased natural killer cell activity in experimental American trypanosomiasis. J Immunol 1981;127(3):1126–1130.
 
13. Hauser WE Jr, Sharma SD, Remington JS. Natural killer cells induced by acute and chronic toxoplasma infection. Cell Immunol 1982;69(2):330–346.
  
14. Herberman RB, Nunn ME, Lavrin DH. Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic acid allogeneic tumors. I. Distribution of reactivity and specificity. Int J Cancer 1975;16(2):216–229.
  
15. Herberman RB, Ortaldo JR. Natural killer cells: their roles in defenses against disease. Science 1981;214(4516):24–30.
  
16. Jensen J, et al. Arch Derm Res 1982;272:163–167.
 
17. Kato T, Minagawa T. Enhancement of cytotoxicity of human peripheral blood lymphocytes by interferon. Microbiol Immunol 1981;25(8):837–845.
 
18. Kiessling R, Klein E, Wigzell H. "Natural" killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype. Eur J Immunol 1975;5(2):112–117.
  
19. Leung DY, Siegel RL, Grady S, Krensky A, Meade R, Reinherz EL, Geha RS. Immunoregulatory abnormalities in mucocutaneous lymph node syndrome. Clin Immunol Immunopathol 1982;23(1):100–112.
  
20. Martinez J, Duma RJ, Nelson EC, Moretta FL. Experimental naegleria meningoencephalitis in mice. Penetration of the olfactory mucosal epithelium by Naegleria and pathologic changes produced: a light and electron microscope study. Lab Invest 1973;29(2):121–133.
 
21. Pross HF, Pater J, Dwosh I, Giles A, Gallinger LA, Rubin P, Corbett WE, Galbraith P, Baines MG. Studies of human natural killer cells. III. Neutropenia associated with unusual characteristics of antibody-dependent and natural killer cell-mediated cytotoxicity. J Clin Immunol 1982;2(2):126–134.
  
22. Roder JC, Kiessling R, Biberfeld P, Andersson B. Target-effector interaction in the natural killer (NK) cell system. II. The isolation of NK cells and studies on the mechanism of killing. J Immunol 1978;121(6):2509–2517.
 
23. Serdengecti S, Jones DB, Holdstock G, Wright R. Natural killer activity in patients with biopsy-proven liver disease. Clin Exp Immunol 1981;45(2):361–364.
 
24. Timonen T, Ortaldo JR, Herberman RB. Characteristics of human large granular lymphocytes and relationship to natural killer and K cells. J Exp Med 1981;153(3):569–582.
  
25. Ullberg M, Jondal M. Recycling and target binding capacity of human natural killer cells. J Exp Med 1981;153(3):615–628.
  
Editorial Office
Department of Molecular Parasitology, Samsung Medical Center, School of Medicine, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419, Gyeonggi-do, Korea.
Tel: +82-31-299-6251   FAX: +82-1-299-6269   E-mail: kjp.editor@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © 2024 by The Korean Society for Parasitology and Tropical Medicine.     Developed in M2PI