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

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.

[1]  K. Lafferty,et al.  Activation of cytotoxic T cells by nonstimulating tumor cells and spleen cell factor(s). , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Irle Rapid purification of peanut agglutinin by sialic acid-less fetuin-sepharose column. , 1977, Journal of immunological methods.

[3]  M. Raff,et al.  Accessory cell dependence of lectin‐induced proliferation of mouse T lymphocytes , 1977, European journal of immunology.

[4]  P. Vassalli,et al.  Origin and nature of the cells participating in the popliteal graft versus host reaction in mouse and rat. , 1977, Cellular immunology.

[5]  L. Pilarski,et al.  Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A , 1977, The Journal of experimental medicine.

[6]  L. Pilarski A requirement for antigen-specific helper T cells in the generation of cytotoxic T cells from thymocyte precursors , 1977, The Journal of experimental medicine.

[7]  K. Shortman,et al.  The differentiation of T-lymphocytes. III. The behaviour of subpopulations of mouse thymus cells in short-term cell culture. , 1976, Cellular immunology.

[8]  G. Mills,et al.  Proliferation of murine thymic lymphocytes in vitro is mediated by the concanavalin A-induced release of a lymphokine (costimulator). , 1976, Journal of immunology.

[9]  M. Linker-Israeli,et al.  Separation of mouse thymocytes into two subpopulations by the use of peanut agglutinin. , 1976, Cellular immunology.

[10]  H Cantor,et al.  Development and function of subpopulations of thymocytes and T lymphocytes. , 1976, Progress in allergy.

[11]  E. Unanue,et al.  The modulation of lymphocyte functions by molecules secreted by macrophages. II. Conditions leading to increased secretion , 1976, The Journal of experimental medicine.

[12]  T. Tadakuma,et al.  Biological expressions of lymphocyte activation. V. Characterization of a soluble immune response suppressor (SIRS) produced by concanavalin A-activated spleen cells. , 1976, Journal of immunology.

[13]  P. Vassalli,et al.  Synergistic and suppressive interactions among mouse T lymphocytes in the response to phytohemagglutinin , 1975, The Journal of experimental medicine.

[14]  H. Blomgren,et al.  Evidence of Different Cell Populations in the Mouse Thymus Releasing and Responding to Mitogenic Factor , 1975, Scandinavian journal of immunology.

[15]  H. Boehmer,et al.  Subpopulations of T‐Lymphocytes , 1975 .

[16]  E. Unanue,et al.  The modulation of lymphocyte functions by molecules secreted by macrophages. I. Description and partial biochemical analysis , 1975, The Journal of experimental medicine.

[17]  D. M. Chen,et al.  Production by murine spleen cells of an activity stimulating the PHA-responsiveness of thymus lymphocytes. , 1975, Cellular immunology.

[18]  C. Parish,et al.  A procedure for removing red cells and dead cells from lymphoid cell suspensions. , 1975, Journal of immunological methods.

[19]  H. Blomgren,et al.  Characterization of mouse cells releasing or responding to mitogenic factor induced by phytomitogens in vitro. , 1975, Journal of immunology.

[20]  P. Vassalli,et al.  Study of the cells proliferating in parent versus F hybrid mixed lymphocyte culture , 1975, The Journal of experimental medicine.

[21]  M. Cohn,et al.  Cytotoxic effects of antigen- and mitogen-induced T cells on various targets. , 1975, Journal of immunology.

[22]  P. Vassalli,et al.  Mouse bone marrow lymphocytes and their differentiation. , 1974, Journal of immunology.

[23]  K. Shortman,et al.  The differentiation of T lymphocytes. I. Proliferation kinetics and interrelationships of subpopulations of mouse thymus cells. , 1974, Cellular immunology.

[24]  Elizabeth Simpson,et al.  A rapid method for the isolation of functional thymus‐derived murine lymphocytes , 1973, European journal of immunology.

[25]  F. Bach,et al.  A miniaturized mouse mixed leukocyte culture in serum-free and mouse serum supplemented media. , 1973, Journal of immunological methods.

[26]  E. V. Elliott A persistent lymphoid cell population in the thymus. , 1973, Nature: New biology.

[27]  G. Möller,et al.  Mitogen‐induced lymphocyte‐mediated cytotoxicity in vitro: Effect of mitogens selectively activating T or B cells , 1972, European journal of immunology.

[28]  P. Vassalli,et al.  MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS , 1972, The Journal of experimental medicine.

[29]  I. Gery,et al.  POTENTIATION OF THE T-LYMPHOCYTE RESPONSE TO MITOGENS , 1972, The Journal of experimental medicine.

[30]  I. Gery,et al.  POTENTIATION OF THE T-LYMPHOCYTE RESPONSE TO MITOGENS , 1972, The Journal of experimental medicine.

[31]  A. Treves,et al.  Capacity of thymic cells to effect target cell lysis following treatment with concanavalin A. , 1972, Cellular immunology.

[32]  R. Aspinall,et al.  Renewal and fate in the mammalian thymus: Mechanisms and inferences of thymocytokinetics , 1972, European journal of immunology.

[33]  R. E. Click,et al.  Immune responses in vitro. I. Culture conditions for antibody synthesis. , 1972, Cellular immunology.

[34]  I. Gery,et al.  Potentiation of cultured mouse thymocyte responses by factors released by peripheral leucocytes. , 1971, Journal of immunology.

[35]  E. Cronkite,et al.  Antigenic markers on cells leaving calf thymus by way of the efferent lymph and venous blood. , 1971, Journal of immunology.

[36]  W. Burr,et al.  A LYMPH NODE WEIGHT ASSAY FOR THE GRAFTVERSUS- HOST ACTIVITY OF RAT LYMPHOID CELLS , 1970, Transplantation.

[37]  B. Chapuis,et al.  Studies of allograft immunity in mice. I. Induction, development and in vitro assay of cellular immunity. , 1970, Immunology.

[38]  H. Blomgren,et al.  Evidence for a small pool of immunocompetent cells in the mouse thymus. , 1969, Experimental cell research.

[39]  R. Dutton,et al.  IMMUNIZATION OF DISSOCIATED SPLEEN CELL CULTURES FROM NORMAL MICE , 1967, The Journal of experimental medicine.

[40]  O. Stutman Two main features of T-cell development: thymus traffic and postthymic maturation. , 1977, Contemporary topics in immunobiology.

[41]  I. Weissman,et al.  Thymus cell maturation: II. Differentiation of three “mature” subclasses in Vivo , 1975 .

[42]  P. Moorhead,et al.  CHROMOSOME CYTOLOGY. , 1964, Methods in medical research.

[43]  L. Old,et al.  CYTOTOXIC TEST FOR DEMONSTRATION OF MOUSE ANTIBODY. , 1964, Methods in medical research.