Literature DB >> 3499378

Accessory cell functions of dendritic cells and macrophages in the thymic T-cell response to Con A.

Y Hirayama1, K Inaba, S Komatsubara, K Yoshida, J Kawai, K Naito, S Muramatsu.   

Abstract

Accessory cell (A cell) functions of splenic dendritic cells (DC) and peritoneal macrophages (M phi) were investigated in the Con A-stimulated proliferative response of thymic T cells. DC were more efficient as A cells than M phi in respect of their necessary cell numbers, Con A dose and culture period required for optimal response. Con A-pulsed T cells proliferated with the aid of lymphocyte activating factor(s) (LAF) derived from M phi, even in the apparent absence of A cells. Con A-pulsed M phi were superior to unpulsed M phi in the secretion of LAF to induce a high response of Con A-pulsed T cells. A cell activity of M phi in different preparations appeared to parallel the ability to secrete LAF, and was totally abolished by fixation of M phi with paraformaldehyde. The fixation of DC, however, resulted in only a partial reduction of the A cell activity. These results argue that both DC and M phi can serve as A cells in the T-cell response to Con A, but that the mechanism to manifest A cell activity is somewhat different between DC and M phi.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3499378      PMCID: PMC1454135     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  23 in total

Review 1.  The participation of macrophages and macrophage cell lines in the activation of T lymphocytes by mitogens.

Authors:  D L Rosenstreich; S B Mizel
Journal:  Immunol Rev       Date:  1978       Impact factor: 12.988

2.  A rapid method for the isolation of functional thymus-derived murine lymphocytes.

Authors:  M H Julius; E Simpson; L A Herzenberg
Journal:  Eur J Immunol       Date:  1973-10       Impact factor: 5.532

3.  Properties of monoclonal antibodies to mouse Ig allotypes, H-2, and Ia antigens.

Authors:  V T Oi; P P Jones; J W Goding; L A Herzenberg; L A Herzenberg
Journal:  Curr Top Microbiol Immunol       Date:  1978       Impact factor: 4.291

4.  Relationship between production and release of lymphocyte-activating factor (interleukin 1) by murine macrophages. 1. Effects of various agents.

Authors:  I Gery; P Davies; J Derr; N Krett; J A Barranger
Journal:  Cell Immunol       Date:  1981-11-01       Impact factor: 4.868

5.  Cellular synergy in the manifestation of accessory cell activity for in vitro antibody response.

Authors:  K Inaba; K Nakano; S Muramatsu
Journal:  J Immunol       Date:  1981-08       Impact factor: 5.422

6.  Rat dendritic cells function as accessory cells and control the production of a soluble factor required for mitogenic responses of T lymphocytes.

Authors:  W E Klinkert; J H LaBadie; J P O'Brien; C F Beyer; W E Bowers
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

7.  Two distinct factors are required for induction of T-cell growth.

Authors:  E L Larsson; N N Iscove; A Coutinho
Journal:  Nature       Date:  1980-02-14       Impact factor: 49.962

8.  Membrane-associated IL 1-like activity on rat dendritic cells.

Authors:  L M Nagelkerken; P J van Breda Vriesman
Journal:  J Immunol       Date:  1986-03-15       Impact factor: 5.422

9.  Dendritic cells are the principal stimulators of the primary mixed leukocyte reaction in mice.

Authors:  R M Steinman; B Gutchinov; M D Witmer; M C Nussenzweig
Journal:  J Exp Med       Date:  1983-02-01       Impact factor: 14.307

10.  Contribution of dendritic cells to stimulation of the murine syngeneic mixed leukocyte reaction.

Authors:  M C Nussenzweig; R M Steinman
Journal:  J Exp Med       Date:  1980-05-01       Impact factor: 14.307

View more
  1 in total

1.  Phagocytosis and protein processing are required for presentation of Cryptococcus neoformans mitogen to T lymphocytes.

Authors:  R M Syme; J C Spurrell; L L Ma; F H Green; C H Mody
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.