Literature DB >> 301478

Reduced in vitro response to concanavalin A and lipopolysaccharide in senescent mice: a function of reduced number of responding cells.

C Abraham, Y Tal, H Gershon.   

Abstract

The proliferative capacity of spleen cells from C57BL/6J female mice of various ages (3-28 months) to the polyclonal mitogens concanavalin A (Con A) and lipopolysaccharide (LPS) was examined. It was found that both the T and B cell population of the spleen demonstrate an age-related decrease in their capacity to respond in vitro. Peak responses to both mitogens occurs at about 1 year of age. This age-related reduction in response is expressed in the degree of incorporation of [3H]thymidine into DNA, the total number of cells generated in vitro, the number of labeled cells per culture and the number of blast cells per culture. The day of peak response in vitro does not change with age. Studies of the cell cycle of cells responding to Con A and to LPS from 12 and 28-month-old mice demonstrate that the generation time of individual proliferating cells does not alter with age. Nor does it differ for the B cells responding to LPS or the T cells responding to Con A. These studies also demonstrate that the proliferating cells from senescent mice are equally capable of repeated cell divisions as are the cells from the 1-year-old adult mouse. It is concluded that the defect in senescent mice which leads to a reduced in vitro response to the polyclonal mitogens LPS and Con A is a reduction in the number of responding cells and not an alteration in the capacity of those cells which do respond to divide.

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Year:  1977        PMID: 301478     DOI: 10.1002/eji.1830070512

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  8 in total

1.  Immunological senescence. II. Normal in vitro colony formation by B cells from old mice.

Authors:  A K Duwe; J C Roder; S K Singhal
Journal:  Immunology       Date:  1979-06       Impact factor: 7.397

2.  Ageing and immunity in outbred NMRI mice: lack of correlation between age-related decline of the response to T cell mitogens, the antibody response to a T-dependent antigen and lifespan in outbred NMRI mice.

Authors:  F Joncourt; F Kristensen; A L De Weck
Journal:  Clin Exp Immunol       Date:  1981-05       Impact factor: 4.330

Review 3.  Pathogenesis and prevention of native valve infective endocarditis in elderly dental patients.

Authors:  A H Friedlander; C E Marshall
Journal:  Drugs Aging       Date:  1994-04       Impact factor: 3.923

4.  Effect of levamisole on cytotoxic T-cell-mediated immune resistance to L1210 murine leukemia in hyperimmune mice.

Authors:  K Gomi; M Morimoto; T Kataoka
Journal:  Cancer Immunol Immunother       Date:  1984       Impact factor: 6.968

5.  Immunological studies of aging. IV. The contribution of thymic involution to the immune deficiencies of aging mice and reversal with thymopoietin32-36.

Authors:  M C Weksler; J D Innes; G Goldstein
Journal:  J Exp Med       Date:  1978-10-01       Impact factor: 14.307

6.  Preliminary Evidence of Endotoxin Tolerance in Dairy Cows during the Transition Period.

Authors:  Joel Filipe; Alessia Inglesi; Massimo Amadori; Flavia Guarneri; Laura Menchetti; Giulio Curone; Gabriele Brecchia; Daniele Vigo; Federica Riva
Journal:  Genes (Basel)       Date:  2021-11-16       Impact factor: 4.096

7.  Antigen responsiveness of the mature and generative B cell populations of aged mice.

Authors:  D Zharhary; N R Klinman
Journal:  J Exp Med       Date:  1983-04-01       Impact factor: 14.307

8.  Characterization of the blastogenic response to LPS of bovine peripheral blood mononuclear cells.

Authors:  Massimo Amadori; Joel Fernando Soares-Filipe; Federica Riva; Andrea Vitali; Jessica Ruggeri; Nicola Lacetera
Journal:  PLoS One       Date:  2018-10-02       Impact factor: 3.240

  8 in total

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