Abstract
In the present study we investigated the development of natural killer (NK) cell lytic activity, and its correlation with the appearance of cells with large granular lymphocyte (LGL) morphology after bone marrow transplantation (BMT). NK activity was first found 7 days after bone marrow (BM) reconstitution, simultaneously with the appearance of the first LGLs. The number of LGLs, as well as the lytic activity, increased until Day 16 after BM reconstitution, after which they started to decrease, reaching the normal values of controls in 30 days. These early appearing LGLs differed somewhat from mature-type LGLs; they were larger, blast-like cells (found in the lower density fractions of Percoll gradient) and had a basophilic cytoplasma, in contrast to a pale cytoplasm in mature LGLs, but they expressed the asialo GM 1 (AGM 1) antigen like normal NK cells. Those NK cells that appeared first also tended to be lytically more effective than their mature counterparts. Taken together, these data suggest that the correlation between LGL morphology and NK lytic activity also holds true during the development of NK cells from their non-lytic precursors in the bone marrow.
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- Abo T., Balch C. M. A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1). J Immunol. 1981 Sep;127(3):1024–1029. [PubMed] [Google Scholar]
- Biron C. A., Natuk R. J., Welsh R. M. Generation of large granular T lymphocytes in vivo during viral infection. J Immunol. 1986 Mar 15;136(6):2280–2286. [PubMed] [Google Scholar]
- Biron C. A., Pedersen K. F., Welsh R. M. Purification and target cell range of in vivo elicited blast natural killer cells. J Immunol. 1986 Jul 15;137(2):463–471. [PubMed] [Google Scholar]
- Biron C. A., Welsh R. M. Blastogenesis of natural killer cells during viral infection in vivo. J Immunol. 1982 Dec;129(6):2788–2795. [PubMed] [Google Scholar]
- Hurme M., Sihvola M. Development of natural killer cells: comparison of the maturation rates in different lymphoid compartments. Scand J Immunol. 1985 Feb;21(2):159–165. doi: 10.1111/j.1365-3083.1985.tb01415.x. [DOI] [PubMed] [Google Scholar]
- Hurme M., Sihvola M. High expression of the Thy-1 antigen on natural killer cells recently derived from bone marrow. Cell Immunol. 1984 Apr 1;84(2):276–284. doi: 10.1016/0008-8749(84)90099-6. [DOI] [PubMed] [Google Scholar]
- Hurme M., Sihvola M. Natural killer (NK) cell activity during lymphatic regeneration: early appearance of Thy-1+ NK cells and highly interleukin 2-(IL 2) receptive, Thy-1- cells. J Immunol. 1983 Aug;131(2):658–661. [PubMed] [Google Scholar]
- Itoh K., Suzuki R., Umezu Y., Hanaumi K., Kumagai K. Studies of murine large granular lymphocytes. II. Tissue, strain, and age distributions of LGL and LAL. J Immunol. 1982 Jul;129(1):395–405. [PubMed] [Google Scholar]
- Kasai M., Iwamori M., Nagai Y., Okumura K., Tada T. A glycolipid on the surface of mouse natural killer cells. Eur J Immunol. 1980 Mar;10(3):175–180. doi: 10.1002/eji.1830100304. [DOI] [PubMed] [Google Scholar]
- 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 Feb;5(2):112–117. doi: 10.1002/eji.1830050208. [DOI] [PubMed] [Google Scholar]
- Koo G. C., Jacobson J. B., Hammerling G. J., Hammerling U. Antigenic profile of murine natural killer cells. J Immunol. 1980 Sep;125(3):1003–1006. [PubMed] [Google Scholar]
- Koo G. C., Peppard J. R., Mark W. H. Natural killer cells generated from bone marrow culture. J Immunol. 1984 May;132(5):2300–2304. [PubMed] [Google Scholar]
- Kumagai K., Itoh K., Suzuki R., Hinuma S., Saitoh F. Studies of murine large granular lymphocytes. I. Identification as effector cells in NK and K cytotoxicities. J Immunol. 1982 Jul;129(1):388–394. [PubMed] [Google Scholar]
- Lanier L. L., Le A. M., Civin C. I., Loken M. R., Phillips J. H. The relationship of CD16 (Leu-11) and Leu-19 (NKH-1) antigen expression on human peripheral blood NK cells and cytotoxic T lymphocytes. J Immunol. 1986 Jun 15;136(12):4480–4486. [PubMed] [Google Scholar]
- Lotzová E., Savary C. A., Lowlachi M., Murasko D. M. Cytotoxic and morphologic profile of endogenous and pyrimidinone-activated murine NK cells. J Immunol. 1986 Jan;136(2):732–740. [PubMed] [Google Scholar]
- Luini W., Boraschi D., Alberti S., Aleotti A., Tagliabue A. Morphological characterization of a cell population responsible for natural killer activity. Immunology. 1981 Aug;43(4):663–668. [PMC free article] [PubMed] [Google Scholar]
- Minato N., Reid L., Bloom B. R. On the heterogeneity of murine natural killer cells. J Exp Med. 1981 Sep 1;154(3):750–762. doi: 10.1084/jem.154.3.750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Patel M. R., Linna T. J. Enrichment of mouse splenic natural killer cells using discontinuous polyvinylpyrrolidone silica (Percoll) gradients. Immunology. 1984 Dec;53(4):721–729. [PMC free article] [PubMed] [Google Scholar]
- Perussia B., Starr S., Abraham S., Fanning V., Trinchieri G. Human natural killer cells analyzed by B73.1, a monoclonal antibody blocking Fc receptor functions. I. Characterization of the lymphocyte subset reactive with B73.1. J Immunol. 1983 May;130(5):2133–2141. [PubMed] [Google Scholar]
- Pollack S. B., Tam M. R., Nowinski R. C., Emmons S. L. Presence of T cell-associated surface antigens on murine NK cells. J Immunol. 1979 Oct;123(4):1818–1821. [PubMed] [Google Scholar]
- Renkonen R., Häyry P. Bone marrow transplantation in the rat. I. Histologic correlations and quantitation of cellular infiltrates in acute graft-versus-host disease. Am J Pathol. 1984 Dec;117(3):462–470. [PMC free article] [PubMed] [Google Scholar]
- Reynolds C. W., Timonen T., Herberman R. B. Natural killer (NK) cell activity in the rat. I. Isolation and characterization of the effector cells. J Immunol. 1981 Jul;127(1):282–287. [PubMed] [Google Scholar]
- Santoni A., Piccoli M., Ortaldo J. R., Mason L., Wiltrout R. H., Herberman R. B. Changes in number and density of large granular lymphocytes upon in vivo augmentation of mouse natural killer activity. J Immunol. 1985 Apr;134(4):2799–2810. [PubMed] [Google Scholar]
- Sihvola M. Lymphokine-activated killer cells in mouse bone marrow chimaeras. The relationship to natural killer cells and to alloreactive cytotoxic T cells. Scand J Immunol. 1985 Nov;22(5):479–488. doi: 10.1111/j.1365-3083.1985.tb01906.x. [DOI] [PubMed] [Google Scholar]
- Silvennoinen O., Renkonen R., Hurme M. Characterization of natural killer cells and their precursors in the murine bone marrow. Cell Immunol. 1986 Aug;101(1):1–7. doi: 10.1016/0008-8749(86)90180-2. [DOI] [PubMed] [Google Scholar]
- Suttles J., Schwarting G. A., Stout R. D. Flow cytometric analysis reveals the presence of asialo GM1 on the surface membrane of alloimmune cytotoxic T lymphocytes. J Immunol. 1986 Mar 1;136(5):1586–1591. [PubMed] [Google Scholar]
- Tagliabue A., Befus A. D., Clark D. A., Bienenstock J. Characteristics of natural killer cells in the murine intestinal epithelium and lamina propria. J Exp Med. 1982 Jun 1;155(6):1785–1796. doi: 10.1084/jem.155.6.1785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Timonen T., Saksela E., Ranki A., Häyry P. Fractionation, morphological and functional characterization of effector cells responsible for human natural killer activity against cell-line targets. Cell Immunol. 1979 Nov;48(1):133–148. doi: 10.1016/0008-8749(79)90106-0. [DOI] [PubMed] [Google Scholar]
- Velardi A., Grossi C. E., Cooper M. D. A large subpopulation of lymphocytes with T helper phenotype (Leu-3/T4+) exhibits the property of binding to NK cell targets and granular lymphocyte morphology. J Immunol. 1985 Jan;134(1):58–64. [PubMed] [Google Scholar]
- Wiltrout R. H., Mathieson B. J., Talmadge J. E., Reynolds C. W., Zhang S. R., Herberman R. B., Ortaldo J. R. Augmentation of organ-associated natural killer activity by biological response modifiers. Isolation and characterization of large granular lymphocytes from the liver. J Exp Med. 1984 Nov 1;160(5):1431–1449. doi: 10.1084/jem.160.5.1431. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiltrout R. H., Santoni A., Peterson E. S., Knott D. C., Overton W. R., Herberman R. B., Holden H. T. Reactivity of anti-asialo GM1 serum with tumoricidal and non-tumoricidal mouse macrophages. J Leukoc Biol. 1985 May;37(5):597–614. doi: 10.1002/jlb.37.5.597. [DOI] [PubMed] [Google Scholar]
- Zarling J. M., Clouse K. A., Biddison W. E., Kung P. C. Phenotypes of human natural killer cell populations detected with monoclonal antibodies. J Immunol. 1981 Dec;127(6):2575–2580. [PubMed] [Google Scholar]
- Zöller M., Wigzell H. Normally occurring inhibitory cells for natural killer cell activity. I. Organ distribution. Cell Immunol. 1982 Nov 15;74(1):14–26. doi: 10.1016/0008-8749(82)90002-8. [DOI] [PubMed] [Google Scholar]

