Literature DB >> 1679836

The majority of CD4+8- thymocytes are functionally immature.

F Ramsdell1, M Jenkins, Q Dinh, B J Fowlkes.   

Abstract

The thymus is the major site of T cell development and repertoire selection. During these processes, T cells segregate into two subsets that express either CD4 or CD8 accessory molecules, the phenotype of peripheral T cells. Analysis of CD4+8- thymocytes revealed that the majority of these cells express the heat-stable Ag (HSA) but not the nonclassical class I Ag, Qa-2. This HSA+, Qa-2- phenotype is similar to that of the less mature, CD4+8+ thymocytes. The remaining CD4+8- thymocytes possess the HSA-, Qa-2+ phenotype of peripheral T cells. To determine whether the Qa-2-, CD4+8- thymic subset is fully mature, we have analyzed the functional status of these CD4+8- subpopulations. The results indicate that only those thymocytes which express Qa-2 are fully responsive to anti-TCR stimulation in a manner analogous to peripheral T cells. The Qa-2- subset is nonresponsive to stimulation by anti-TCR antibodies that have been immobilized to plastic, even in the presence of lymphokines or syngeneic APC. This subset is, however, capable of proliferating to allogeneic cells or to anti-TCR on the surface of syngeneic APC, although not to the levels achieved by Qa-2+ thymocytes. Thus, the Qa-2- subset appears to require additional interactions which are not necessary for peripheral T cells or Qa-2+ thymocytes. Relevant to this issue, the Qa-2+ thymocyte subset does not appear until relatively late in development, and does not reach adult frequencies until several weeks after birth. These results would suggest that there is a progression from HSA+, Qa-2- to HSA-, Qa-2+ which parallels the maturation of functional responsiveness. These findings are important to understanding T cell selection since thymocytes with such a decreased responsiveness may have a differential capacity for tolerance induction. The results presented suggest that the bulk of CD4+8- thymocytes are not fully mature and that Qa-2 may serve as a marker for T cells with a more complete functional competence.

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Year:  1991        PMID: 1679836

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  39 in total

1.  Phenotypic identification of the subgroups of murine T-cell receptor alphabeta+ CD4+ CD8- thymocytes and its implication in the late stage of thymocyte development.

Authors:  Q Ge; W F Chen
Journal:  Immunology       Date:  1999-08       Impact factor: 7.397

2.  Phenotypic and functional immaturity of human umbilical cord blood T lymphocytes.

Authors:  D T Harris; M J Schumacher; J Locascio; F J Besencon; G B Olson; D DeLuca; L Shenker; J Bard; E A Boyse
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-01       Impact factor: 11.205

3.  Coordinate change in phenotype in a mouse cell line selected for CD8 expression.

Authors:  R Hyman; V Stallings
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

Review 4.  GRAIL: a unique mediator of CD4 T-lymphocyte unresponsiveness.

Authors:  Chan C Whiting; Leon L Su; Jack T Lin; C Garrison Fathman
Journal:  FEBS J       Date:  2010-11-16       Impact factor: 5.542

5.  Molecular signature of recent thymic selection events on effector and regulatory CD4+ T lymphocytes.

Authors:  Paola Romagnoli; Denis Hudrisier; Joost P M van Meerwijk
Journal:  J Immunol       Date:  2005-11-01       Impact factor: 5.422

6.  Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development.

Authors:  Xiaoming Feng; Gregory C Ippolito; Lifeng Tian; Karla Wiehagen; Soyoung Oh; Arivazhagan Sambandam; Jessica Willen; Ralph M Bunte; Shanna D Maika; June V Harriss; Andrew J Caton; Avinash Bhandoola; Philip W Tucker; Hui Hu
Journal:  Blood       Date:  2009-11-12       Impact factor: 22.113

7.  Developmental changes predispose the fetal thymus to positive selection of CD4+CD8- T cells.

Authors:  P J Fairchild; J M Austyn
Journal:  Immunology       Date:  1995-06       Impact factor: 7.397

8.  LKB1 regulates TCR-mediated PLCγ1 activation and thymocyte positive selection.

Authors:  Yonghao Cao; Hai Li; Haifeng Liu; Min Zhang; Zichun Hua; Hongbin Ji; Xiaolong Liu
Journal:  EMBO J       Date:  2011-04-12       Impact factor: 11.598

9.  Incomplete endoplasmic reticulum (ER) retention in immature thymocytes as revealed by surface expression of "ER-resident" molecular chaperones.

Authors:  D L Wiest; A Bhandoola; J Punt; G Kreibich; D McKean; A Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

10.  Developmental pathway of CD4+CD8- medullary thymocytes during mouse ontogeny and its defect in Aire-/- mice.

Authors:  Juan Li; Yan Li; Jin-Yan Yao; Rong Jin; Ming-Zhao Zhu; Xiao-Ping Qian; Jun Zhang; Yang-Xin Fu; Li Wu; Yu Zhang; Wei-Feng Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-05       Impact factor: 11.205

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