Comparative response of normal human thymus and lymph node cells to phytohemagglutinin in culture.

Human thymocytes, in short-term tissue culture, show a proliferative activity distinct from that observed by either lymph node or blood lymphocytes. As expected, the behavior of lymph node lymphocytes in culture is very similar to that of peripheral blood lymphocytes. The only difference between these 2 groups of cells was the finding of spontaneous proliferation by normal lymph node cells after 3 days in culture without phytohemagglutinin (PHA). Whereas blood and lymph node lymphocytes show a negligible uptake of H3T in the basal state, approximately 10 per cent of thymus cells incorporate H3T, indicating significant autonomous proliferation. This is unaffected by PHA and is unassociated with globulin synthesis as judged by immunofluorescent technics. After 3 days in culture, there are significantly more transformed cells and more cells which incorporate H3T into DNA in thymus cell cultures containing PHA than in the control cultures. However, the labeling index of stimulated thymus cultures is less than either the basal rate of proliferation of thymocytes or 3-day cultures of PHA stimulated blood and lymph node lymphocytes. These observations suggest that the normal human thymus contains at least two populations of lymphoid cells: a major component which shows autonomous and unsustained proliferative activity and does not respond to PHA, and a second and probably minor cellular component which transforms and proliferates in response to PHA.

[1]  O. Mcintyre,et al.  P.HA. and thymic lymphocytes. , 1966, Lancet.

[2]  M. Sasaki,et al.  Proliferation of Human Lymphocytes in Culture , 1966, Nature.

[3]  M. Matsuyama,et al.  AUTORADIOGRAPHIC ANALYSIS OF LYMPHOPOIESIS AND LYMPHOCYTE MIGRATION IN MICE BEARING MULTIPLE THYMUS GRAFTS , 1966, The Journal of experimental medicine.

[4]  H. Sosin,et al.  The immunologic competence of mouse thymus cells measured by the graft vs. host spleen assay. , 1966, Journal of immunology.

[5]  J. Miller,et al.  THE THYMUS AND TRANSPLANTATION IMMUNITY. , 1965, British medical bulletin.

[6]  D. Quaglino,et al.  Autoradiographic Investigations of RNA and DNA Metabolism of Human Leucocytes Cultured with Phytohæmagglutinin ; Uridine-5-3h as a Specific Precursor of RNA , 1965, Nature.

[7]  G. Nossal STUDIES ON THE RATE OF SEEDING OF LYMPHOCYTES FROM THE INTACT GUINEA PIG THYMUS * , 1964, Annals of the New York Academy of Sciences.

[8]  R. G. Murray,et al.  Studies on the fate of lymphocytes III. The migration and metamorphosis of in situ labeled thymic lymphocytes , 1964 .

[9]  H. Fukuta,et al.  PROLIFERATIVE ACTIVITY OF THE LYMPHATIC TISSUES OF RATS AS STUDIED WITH TRITIUM-LABELED THYMIDINE , 1964, The Journal of experimental medicine.

[10]  J. Leddy,et al.  GAMMA-2, GAMMA-1A AND GAMMA-1M ANTINUCLEAR FACTORS IN HUMAN SERA. , 1964, The Journal of clinical investigation.

[11]  O. Nygaard,et al.  The conversion of thymidine to thymine nucleotides and deoxyribonucleic acid in vivo. , 1963, The Journal of biological chemistry.

[12]  S. Roath,et al.  THE RESPONSE OF LYMPHOCYTES TO ANTIGEN CHALLENGE IN VITRO , 1963 .

[13]  C. E. Ford,et al.  Initiation of Immune Responses by Small Lymphocytes , 1962, Nature.

[14]  G. Brecher,et al.  The kinetics of cell proliferation in cultures of human peripheral blood. , 1962, Blood.

[15]  J. Gowans The recirculation of lymphocytes from blood to lymph in the rat , 1959, The Journal of physiology.