Aged human T cells. Suppressed mitogenic response to activation via CD2 and CD3 receptors. 1992

E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
Ponce School of Medicine, Puerto Rico 00732.

UI MeSH Term Description Entries
D008213 Lymphocyte Activation Morphologic alteration of small B LYMPHOCYTES or T LYMPHOCYTES in culture into large blast-like cells able to synthesize DNA and RNA and to divide mitotically. It is induced by INTERLEUKINS; MITOGENS such as PHYTOHEMAGGLUTININS, and by specific ANTIGENS. It may also occur in vivo as in GRAFT REJECTION. Blast Transformation,Blastogenesis,Lymphoblast Transformation,Lymphocyte Stimulation,Lymphocyte Transformation,Transformation, Blast,Transformation, Lymphoblast,Transformation, Lymphocyte,Activation, Lymphocyte,Stimulation, Lymphocyte
D010835 Phytohemagglutinins Mucoproteins isolated from the kidney bean (Phaseolus vulgaris); some of them are mitogenic to lymphocytes, others agglutinate all or certain types of erythrocytes or lymphocytes. They are used mainly in the study of immune mechanisms and in cell culture. Kidney Bean Lectin,Kidney Bean Lectins,Lectins, Kidney Bean,Phaseolus vulgaris Lectin,Phaseolus vulgaris Lectins,Phytohemagglutinin,Hemagglutinins, Plant,Lectin, Kidney Bean,Lectin, Phaseolus vulgaris,Lectins, Phaseolus vulgaris,Plant Hemagglutinins
D011971 Receptors, Immunologic Cell surface molecules on cells of the immune system that specifically bind surface molecules or messenger molecules and trigger changes in the behavior of cells. Although these receptors were first identified in the immune system, many have important functions elsewhere. Immunologic Receptors,Immunologic Receptor,Immunological Receptors,Receptor, Immunologic,Receptors, Immunological
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000945 Antigens, Differentiation, T-Lymphocyte Antigens expressed on the cell membrane of T-lymphocytes during differentiation, activation, and normal and neoplastic transformation. Their phenotypic characterization is important in differential diagnosis and studies of thymic ontogeny and T-cell function. Antigens, Differentiation, T-Cell,Differentiation Antigens, T-Cell,L3T4 Antigens,Leu Antigens, T-Lymphocyte,T-Cell Differentiation Antigens,T-Lymphocyte Differentiation Antigens,T6 Antigens,Antigens, Differentiation, T Lymphocyte,Differentiation Antigens, T Lymphocyte,Antigens, L3T4,Antigens, T-Cell Differentiation,Antigens, T-Lymphocyte Differentiation,Antigens, T-Lymphocyte Leu,Antigens, T6,Differentiation Antigens, T Cell,Differentiation Antigens, T-Lymphocyte,Leu Antigens, T Lymphocyte,T Cell Differentiation Antigens,T Lymphocyte Differentiation Antigens,T-Lymphocyte Leu Antigens
D013601 T-Lymphocytes Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen. T Cell,T Lymphocyte,T-Cells,Thymus-Dependent Lymphocytes,Cell, T,Cells, T,Lymphocyte, T,Lymphocyte, Thymus-Dependent,Lymphocytes, T,Lymphocytes, Thymus-Dependent,T Cells,T Lymphocytes,T-Cell,T-Lymphocyte,Thymus Dependent Lymphocytes,Thymus-Dependent Lymphocyte
D016922 Cellular Senescence Process by which cells irreversibly stop dividing and enter a state of permanent growth arrest without undergoing CELL DEATH. Senescence can be induced by DNA DAMAGE or other cellular stresses, such as OXIDATIVE STRESS. Aging, Cell,Cell Aging,Cell Senescence,Replicative Senescence,Senescence, Cellular,Senescence, Replicative,Cell Ageing,Cellular Ageing,Cellular Aging,Ageing, Cell,Ageing, Cellular,Aging, Cellular,Senescence, Cell
D017252 CD3 Complex Complex of at least five membrane-bound polypeptides in mature T-lymphocytes that are non-covalently associated with one another and with the T-cell receptor (RECEPTORS, ANTIGEN, T-CELL). The CD3 complex includes the gamma, delta, epsilon, zeta, and eta chains (subunits). When antigen binds to the T-cell receptor, the CD3 complex transduces the activating signals to the cytoplasm of the T-cell. The CD3 gamma and delta chains (subunits) are separate from and not related to the gamma/delta chains of the T-cell receptor (RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA). Antigens, CD3,CD3 Antigens,T3 Antigens,CD3 Antigen,T3 Antigen,T3 Complex,Antigen, CD3,Antigen, T3,Antigens, T3
D018801 CD2 Antigens Glycoprotein members of the immunoglobulin superfamily which participate in T-cell adhesion and activation. They are expressed on most peripheral T-lymphocytes, natural killer cells, and thymocytes, and function as co-receptors or accessory molecules in the T-cell receptor complex. Antigens, CD2,T11 Erythrocyte-Binding Glycoprotein,CD2 Antigen,Antigen, CD2,Erythrocyte-Binding Glycoprotein, T11,T11 Erythrocyte Binding Glycoprotein

Related Publications

E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
May 1989, European journal of immunology,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
July 1988, The EMBO journal,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
November 1988, The Journal of experimental medicine,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
September 1985, Journal of immunology (Baltimore, Md. : 1950),
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
May 1988, Scandinavian journal of immunology,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
September 1986, Journal of immunology (Baltimore, Md. : 1950),
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
October 1990, European journal of immunology,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
January 1990, International immunology,
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
November 1988, Journal of immunology (Baltimore, Md. : 1950),
E H Eylar, and F Montealegre, and C Molina, and C Rivera-Quñones, and I Baez, and J Díaz, and R Mariño
June 1991, Journal of immunology (Baltimore, Md. : 1950),
Copied contents to your clipboard!