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. 1978 Jul 1;148(1):32–45. doi: 10.1084/jem.148.1.32

In vitro maturation of immature thymocytes into immunocompetent T cells in the absence of direct thymic influence

C Irle, P-F Piguet, P Vassalli
PMCID: PMC2184919  PMID: 78962

Abstract

Peanut lectin (PNL) binds to a majority of mouse thymocytes (Thc) in suspension. By using cell affinity chromatography on a column of anti-PNL antibody, Thc populations at least 96 percent pure in PNL + or - cells, as judged by immunofluorescence, were obtained. PNL(+) cells are rich in Thy 1 and poor in H(2) antigens, cortisone sensitive, unresponsive to phytohemagglutinin (PHA), and immunologically incompetent, as judged by mixed lymphocyte reaction, popliteal lymph node graft-versus-host assay, and by testing helper activity in a primary in vitro antibody response to sheep erythrocytes; the converse is true of PNL(-) cells. Thus, PNL(+) and (-) cells appear to correspond to cortical and medullary Thc, respectively, as previously suggested. In culture, PNL(+) Thc show poor viability and a weak proliferative response to concanavalin A (Con A), except when supernate (SUP) of 24 h Con A stimulated lymph node lymphocyte cultures, or irradiated lymph node cells, are added, in which cases a strong proliferative response to the mitogen is observed. A variety of control experiments showed that the proliferating cells did not result from preferential stimulation of a few contaminating PNL(-) Thc present in the PNL(+) Thc cultures. The blasts resulting from PNL(+) Thc proliferation display mitogen-induced cytotoxicity, and give rise to a population of medium-sized lymphocytes, mostly PNL(-), poor in Thy 1 and rich in H(2) antigens, PHA responsive, and immunologically competent in the above-mentioned assays. Fresh PNL(+) Thc responded in mixed lymphocyte reaction in the presence of SUP (lectin depleted) and since incubation in SUP alone did not confer reactivity on PNL(+) Thc, it appears therefore that (a) immature Thc possess alloantigen and mitogen-specific surface receptors but lack the capacity to respond by proliferation to receptor triggering without the help of extracellular factor(s) released by mature lymphoid cells stimulated by mitogens (b) cell division is associated with the acquisition of immunological responsiveness, characteristic of mature T lymphocytes. The implications of these findings for the ontogenesis of thymus-derived lymphocytes, and for the possible traffic of Thc within and from the thymus, are discussed.

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Selected References

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  1. Bevan M. J., Cohn M. Cytotoxic effects of antigen- and mitogen-induced T cells on various targets. J Immunol. 1975 Feb;114(2 Pt 1):559–565. [PubMed] [Google Scholar]
  2. Blomgren H., Andersson B. Evidence for a small pool of immunocompetent cells in the mouse thymus. Exp Cell Res. 1969 Oct;57(2):185–192. doi: 10.1016/0014-4827(69)90140-2. [DOI] [PubMed] [Google Scholar]
  3. Brunner K. T., Mauel J., Rudolf H., Chapuis B. Studies of allograft immunity in mice. I. Induction, development and in vitro assay of cellular immunity. Immunology. 1970 Apr;18(4):501–515. [PMC free article] [PubMed] [Google Scholar]
  4. Bryant B. J. Renewal and fate in the mammalian thymus: mechanisms and inferences of thymocytokinetics. Eur J Immunol. 1972 Feb;2(1):38–45. doi: 10.1002/eji.1830020109. [DOI] [PubMed] [Google Scholar]
  5. Calderon J., Kiely J. M., Lefko J. L., Unanue E. R. The modulation of lymphocyte functions by molecules secreted by macrophages. I. Description and partial biochemical analysis. J Exp Med. 1975 Jul 1;142(1):151–164. doi: 10.1084/jem.142.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cantor H., Weissman I. Development and function of subpopulations of thymocytes and T lymphocytes. Prog Allergy. 1976;20:1–64. [PubMed] [Google Scholar]
  7. Click R. E., Benck L., Alter B. J. Immune responses in vitro. I. Culture conditions for antibody synthesis. Cell Immunol. 1972 Feb;3(2):264–276. doi: 10.1016/0008-8749(72)90165-7. [DOI] [PubMed] [Google Scholar]
  8. Davidson W. F., Parish C. R. A procedure for removing red cells and dead cells from lymphoid cell suspensions. J Immunol Methods. 1975 Jun;7(2-3):291–300. doi: 10.1016/0022-1759(75)90026-5. [DOI] [PubMed] [Google Scholar]
  9. Di Sabato G., Chen D. M., Erickson J. W. Production by murine spleen cells of an activity stimulating the PHA-responsiveness of thymus lymphocytes. Cell Immunol. 1975 Jun;17(2):495–504. doi: 10.1016/s0008-8749(75)80053-0. [DOI] [PubMed] [Google Scholar]
  10. Elliott E. V. A persistent lymphoid cell population in the thymus. Nat New Biol. 1973 Apr 4;242(118):150–152. doi: 10.1038/newbio242150a0. [DOI] [PubMed] [Google Scholar]
  11. Fathman C. G., Small M., Herzenberg L. A., Weissman I. L. Thymus cell maturation. II. Differentiation of three "mature" subclasses in vivo. Cell Immunol. 1975 Jan;15(1):109–128. doi: 10.1016/0008-8749(75)90169-0. [DOI] [PubMed] [Google Scholar]
  12. Ford W. L., Burr W., Simonsen M. A lymph node weight assay for the graft-versus-host activity of rat lymphoid cells. Transplantation. 1970 Sep;10(3):258–266. doi: 10.1097/00007890-197009000-00007. [DOI] [PubMed] [Google Scholar]
  13. Gery I., Gershon R. K., Waksman B. H. Potentiation of cultured mouse thymocyte responses by factors released by peripheral leucocytes. J Immunol. 1971 Dec;107(6):1778–1780. [PubMed] [Google Scholar]
  14. Gery I., Gershon R. K., Waksman B. H. Potentiation of the T-lymphocyte response to mitogens. I. The responding cell. J Exp Med. 1972 Jul 1;136(1):128–142. doi: 10.1084/jem.136.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Habu S., Raff M. C. Accessory cell dependence of lectin-induced proliferation of mouse T lymphocytes. Eur J Immunol. 1977 Jul;7(7):451–457. doi: 10.1002/eji.1830070710. [DOI] [PubMed] [Google Scholar]
  16. Hopper K., Shortman K. The differentiation of T-lymphocytes. III. The behaviour of subpopulations of mouse thymus cells in short-term cell culture. Cell Immunol. 1976 Dec;27(2):256–273. doi: 10.1016/0008-8749(76)90233-1. [DOI] [PubMed] [Google Scholar]
  17. Irle C. Rapid purification of peanut agglutinin by sialic acid-less fetuin-sepharose column. J Immunol Methods. 1977;17(1-2):117–121. doi: 10.1016/0022-1759(77)90082-5. [DOI] [PubMed] [Google Scholar]
  18. Jacobsson H., Blomgren H. Characterization of mouse cells releasing or responding to mitogenic factor induced by phytomitogens in vitro. J Immunol. 1975 May;114(5):1631–1637. [PubMed] [Google Scholar]
  19. Jacobsson H., Blomgren H. Evidence of different cell populations in the mouse thymus releasing and responding to mitogenic factor. Scand J Immunol. 1975;4(8):791–799. doi: 10.1111/j.1365-3083.1975.tb03719.x. [DOI] [PubMed] [Google Scholar]
  20. Julius M. H., Simpson E., Herzenberg L. A. A rapid method for the isolation of functional thymus-derived murine lymphocytes. Eur J Immunol. 1973 Oct;3(10):645–649. doi: 10.1002/eji.1830031011. [DOI] [PubMed] [Google Scholar]
  21. Lamelin J. P., Lisowska-Bernstein B., Matter A., Ryser J. E., Vassalli P. Mouse thymus-independent and thymus-derived lymphoid cells. I. Immunofluorescent and functional studies. J Exp Med. 1972 Nov 1;136(5):984–1007. doi: 10.1084/jem.136.5.984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. MOORHEAD P. S., NOWELL P. C. CHROMOSOME CYTOLOGY. Methods Med Res. 1964;10:310–322. [PubMed] [Google Scholar]
  23. Mishell R. I., Dutton R. W. Immunization of dissociated spleen cell cultures from normal mice. J Exp Med. 1967 Sep 1;126(3):423–442. doi: 10.1084/jem.126.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Möller G., Sjöberg O., Andersson J. Mitogen-induced lymphocyte-mediated cytotoxicity in vitro: effect of mitogens selectively activating T or B cells. Eur J Immunol. 1972 Dec;2(6):586–592. doi: 10.1002/eji.1830020621. [DOI] [PubMed] [Google Scholar]
  25. Paetkau V., Mills G., Gerhart S., Monticone V. Proliferation of murine thymic lymphocytes in vitro is mediated by the concanavalin A-induced release of a lymphokine (costimulator). J Immunol. 1976 Oct;117(4):1320–1324. [PubMed] [Google Scholar]
  26. Peck A. B., Bach F. H. A miniaturized mouse mixed leukocyte culture in serum-free and mouse serum supplemented media. J Immunol Methods. 1973 Oct;3(2):147–163. doi: 10.1016/0022-1759(73)90030-6. [DOI] [PubMed] [Google Scholar]
  27. Piguet P. F., Dewey H. K., Vassalli P. Origin and nature of the cells participating in the popliteal graft versus host reaction in mouse and rat. Cell Immunol. 1977 Jun 15;31(2):242–254. doi: 10.1016/0008-8749(77)90026-0. [DOI] [PubMed] [Google Scholar]
  28. Piguet P. F., Dewey H. K., Vassalli P. Study of the cells proliferating in parent versus F hybrid mixed lymphocyte culture. J Exp Med. 1975 Apr 1;141(4):775–787. [PMC free article] [PubMed] [Google Scholar]
  29. Piguet P. F., Dewey H. K., Vassalli P. Synergistic and suppressive interactions among mouse T lymphocytes in the response to phytohemagglutinin. J Exp Med. 1975 Dec 1;142(6):1591–1599. doi: 10.1084/jem.142.6.1591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Pilarski L. M. A requirement for antigen-specific helper T cells in the generation of cytotoxic T cells from thymocyte precursors. J Exp Med. 1977 Mar 1;145(3):709–725. doi: 10.1084/jem.145.3.709. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Pilarski L. M., Bretscher P. A., Baum L. L. Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A. J Exp Med. 1977 May 1;145(5):1237–1249. doi: 10.1084/jem.145.5.1237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Reisner Y., Linker-Israeli M., Sharon N. Separation of mouse thymocytes into two subpopulations by the use of peanut agglutinin. Cell Immunol. 1976 Jul;25(1):129–134. doi: 10.1016/0008-8749(76)90103-9. [DOI] [PubMed] [Google Scholar]
  33. Ryser J. E., Vassalli P. Mouse bone marrow lymphocytes and their differentiation. J Immunol. 1974 Sep;113(3):719–728. [PubMed] [Google Scholar]
  34. Shortman K., Jackson H. The differentiation of T lymphocytes. I. Proliferation kinetics and interrelationships of subpopulations of mouse thymus cells. Cell Immunol. 1974 May;12(2):230–246. doi: 10.1016/0008-8749(74)90075-6. [DOI] [PubMed] [Google Scholar]
  35. Shortman K., Von Boehmer H., Lipp J., Hopper K. Subpopulations of T-lymphocytes. Physical separation, functional specialisation and differentiation pathways of sub-sets of thymocytes and thymus-dependent peripheral lymphocytes. Transplant Rev. 1975;25:163–210. [PubMed] [Google Scholar]
  36. Stavy L., Treves A. J., Feldman M. Capacity of thymic cells to effect target cell lysis following treatment with concanavalin A. Cell Immunol. 1972 Apr;3(4):623–628. doi: 10.1016/0008-8749(72)90124-4. [DOI] [PubMed] [Google Scholar]
  37. Stutman O. Two main features of T-cell development: thymus traffic and postthymic maturation. Contemp Top Immunobiol. 1977;7:1–46. doi: 10.1007/978-1-4684-3054-7_1. [DOI] [PubMed] [Google Scholar]
  38. Tadakuma T., Kühner A. L., Rich R. R., David J. R., Pierce C. W. Biological expressions of lymphocyte activation. V. Characterization of a soluble immune response suppressor (SIRS) produced by concanavalin A-activated spleen cells. J Immunol. 1976 Jul;117(1):323–330. [PubMed] [Google Scholar]
  39. Talmage D. W., Woolnough J. A., Hemmingsen H., Lopez L., Lafferty K. J. Activation of cytotoxic T cells by nonstimulating tumor cells and spleen cell factor(s). Proc Natl Acad Sci U S A. 1977 Oct;74(10):4610–4614. doi: 10.1073/pnas.74.10.4610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Unanue E. R., Kiely J. M., Calderon J. The modulation of lymphocyte functions by molecules secreted by macrophages. II. Conditions leading to increased secretion. J Exp Med. 1976 Jul 1;144(1):155–166. doi: 10.1084/jem.144.1.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Weissman I. L. Thymus cell maturation. Studies on the origin of cortisone-resistant thymic lymphocytes. J Exp Med. 1973 Feb 1;137(2):504–510. doi: 10.1084/jem.137.2.504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Williams R. M., Chanana A. D., Cronkite E. P., Waksman B. H. Antigenic markers on cells leaving calf thymus by way of the efferent lymph and venous blood. J Immunol. 1971 May;106(5):1143–1146. [PubMed] [Google Scholar]

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