New data on the cytolytic effects of natural killer cells (Kurloff cells) on a leukemic cell line (guinea pig L2C)

Leukemia Research

Volumn 23, Issue 2, 1999, Pages 137-147

  Debout, Claire ^a   Quillec, Michèle ^a   Izard, Jacques ^a  

^a UNIVERSITÉ DE CAEN   (France)

Author keywords

Apoptosis; Effector target conjugate; Kurloff cell; Leukemia; Natural killer; Necrosis

Indexed keywords

ANIMAL CELL; APOPTOSIS; ARTICLE; CANCER CELL CULTURE; CONTROLLED STUDY; CYTOLYSIS; DNA DEGRADATION; ENZYME ACTIVITY; GUINEA PIG; LEUKEMIA CELL; LEUKEMOGENESIS; NATURAL KILLER CELL; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; APOPTOSIS; DEXAMETHASONE; DNA FRAGMENTATION; GUINEA PIGS; KILLER CELLS, NATURAL; LEUKEMIA, EXPERIMENTAL; MICROSCOPY, ELECTRON; NECROSIS; PHOSPHATIDYLSERINES; TUMOR CELLS, CULTURED;

EID: 0032927389     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(98)00155-6     Document Type: Article

References (39)

1. Trinchieri G. Biology of natural killer cells. Adv. Immunol. 47:1989;187.
2. Herberman R.B., Reynolds C.W., Ortaldo J.R. Mechanism of cytotoxicity of natural killer cells. Ann. Rev. Immunol. 4:1986;651.
3. Lanier L.L. Follow the leader: NK cell receptors for classical and nonclassical MHC class I. Cell. 92:1998;705.
4. Valiante N.M., Lienert K., Shilling H. G., Smits B. J., Parham P. Killer cell receptors: keeping pace with MHC class I evolution. Immunol. Rev. 155:1997;155.
5. Khar A., Pardhasaradhi B.V.V., Varalakshmi Ch. Mubarak A., Kumari A.L. Natural killer cell as the effector which mediates in vivo apoptosis in AK-5 tumor cells. Cell. Immunol. 177:1997;86.
6. Landemore G., Quillec M., Letaief S.E., Izard J. The proteoglycan squeleton of the Kurloff body as evidenced by cuprolinic blue staining. Histochem. J. 26:1994;571.
7. Taouji S., Buat M.L., Izard J., Landemore G. Kurloff cell lysosomal arylsulfatases: presence of both cationic and highly anionic isoforms of the sole B class. Biol. Cell. 80:1994;43.
8. Debout C., Quillec M., Izard J. Natural killer activity of Kurloff cells: a direct demonstration on purified Kurloff cell suspensions. Cell. Immunol. 87:1984;674.
9. Pouliot N, Magni K, Sirois P, Rolapleszczynki M. FASEB J. 1990:4;A-1892 (abstract).
10. Debout C., Birebent B., Griveau A.M., Izard J. In vitro effect of guinea pig natural killer (Kurloff cells) on homologous leukemic cells (L2C). Leukemia. 7:1993;733.
11. Murphy S.G., Lobuglio A.F. L2C leukemia: a model of human acute leukemia. Fed. Proc. Fedn Am. Soc. Exp. Biol. 36:1977;2281.
12. - lymphocyte with natural killer activity. Nat. Immun. Cell Growth Regul. 10:1991;327.
13. ++ dependency. Inflammation. 20:1996;647.
14. Debout C., Taouji S., Izard J. Increase of a guinea pig natural killer cell (Kurloff cell) during leukemogenesis. Cancer Lett. 97:1995;117.
15. Taouji S., Debout C., Izard J. Arylsulfatases B in Kurloff cells: increasing activity of anionic isoforms in guinea pig acute lymphoblastic leukemia. Leukemia Res. 20:1996;259.
16. Darzynkiewicz Z., Bruno S., Del Bino G., Gorczyca W., Hotz M.A., Lassota P., Traganos F. Features of apoptotic cells measured by flow cytometry. Cytometry. 13:1992;795.
17. Kang H.Y., Carl M., Watson L.P., Yaffe L. Immunoultrastructural studies of human NK cells: II. Effector-target cell binding and phagocytosis. Anat. Rec. 217:1987;290.
18. 35S-methionine of these cells. Biol. Cell. 50:1984;121.
19. Miller S.A., Dykes D.D., Polesky H.F. A simple salting out procedure for extraction DNA from human nucleated cells. Nucleic Acids Res. 16:1988;1215.
20. Mc Kelvey-Martin V.J., Green M.H.L., Schmezer P., Pool-Zobel B.L., De Meo M.P., Collins A. The single cell gel electrophoresis assay (comet assay): a european review. Mutation Res. 288:1993;47.
21. Fairbairn D.W., Olive P.L., O'Neill K.L. The comet assay: a comprehensive review. Mutation Res. 339:1995;37.
22. Gavrieli Y., Sherman Y., Ben-Sasson S.A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J. Cell Biol. 119:1992;493.
23. Vermes I., Haanen C., Steffens-Nakken H., Reutelingsperger C. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labeled Annexin V. J. Immunol. Methods. 184:1995;39.
24. Hertveldt K., Philippé J., Thierens H., Cornelissen M., Vral A., De Ridder L. Flow cytometry as a quantitative and sensitive method to evaluate low dose radiation induced apoptosis in vitro in human peripheral blood lymphocytes. Int. J. Radiat. Biol. 71:1997;429.
25. Knapp D.W., Turek J.J., DeNicola D.B., Chan T.C.K., Carter W.O., Snyder P.W., Robinson J.P. Ultrastructure and cytochemical staining characteristics of canine natural killer cells. Anat. Rec. 243:1995;509.
26. Khar A. Mechanisms involved in natural killer cell mediated target cell death leading to spontaneous tumour regression. J. Biosci. 22:1997;23.
27. Neighbour P.A., Huberman H.S., Kress Y. Human large granular lymphocytes and natural killing: ultrastructural studies of strontium-induced degranulation. Eur. J. Immunol. 12:1982;588.
28. Mahdi T., Tanzer J., Brizard A., Guilhot F., Babin P., Kitzis A. Cell-mediated cytotoxicity can be regulated by p53 tumor suppressor gene activity in vitro. Biol. Cell. 84:1995;175.
29. Geiger B., Rosen D., Berke G. Spatial relationships of microtubule-organizing centers and the contact area of cytotoxic T lymphocytes and target cells. J. Cell Biol. 95:1982;137.
30. Kupfer A., Dennert G., Singer S.J. The reorientation of the Golgi apparatus and the microtubule-organizing center in the cytotoxic effector cell is a prerequisite in the lysis of bound target cells. J. Mol. Cell Immunol. 2:1985;37.
31. Dive C., Gregory C.D., Phipps D.J., Evans D.L., Milner A.E., Wyllie A.H. Analysis and discrimination of necrosis and apoptosis (programmed cell death) by multiparameter flow cytometry. Biochem. Biophys. Acta. 1133:1992;275.
32. Berendsen P.B. Phagocytic inability of Kurloff cells in the lung and spleen of the guinea pig. Cell Tissue Res. 204:1979;513.
33. Izard J., Barrelier M.T., Quillec M. No relationship between Foà's anf Kurloff's body and erythrophagocytosis. Anat. Rec. 178:1974;516.
34. Cohen G.M., Sun X.M., Snowden R.T., Dinsdale D., Skilleter D.N. Key morphological features of apoptosis may occur in the absence of internucleosomal DNA fragmentation. Biochem. J. 286:1992;331.
35. Fadok V.A., Voelker D.R., Campbell P.A., Cohen J.J., Bratton D.L., Henson P.M. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J. Immunol. 148:1992;2207.
36. Van den Eijnde S.M., Boshart L., Reutenlingsperger C.P.M., De Zeeuw CI., Vermeij-Keers C. Phosphatidylserine plasma membrane asymetry in vivo: a pancellular phenomenom which alters during apoptosis. Cell Death Differentiation. 4:1997;311.
37. Wyllie A.H. Glucocorticoid-induced apoptosis is associated with endogenous endonuclease activation. Nature (London). 284:1980;555.
38. Curnow S. J., Glennie M. J., Stevenson G. T. The role of apoptosis in antibody-dependent cellular cytotoxicity. Cancer Immunol. Immunother. 36:1993;149.
39. Grasl-Kraupp B., Ruttkay-Nedecky B., Koudelka H., Bukowska K., Bursch W., Schulte-Hermann R. In situ detection of fragmented DNA (Tunel assay) fails to discriminate among apoptosis, necrosis, and autolytic cell death: a cautionary note. Hepatology. 21:1995;1465.