Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (10)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Rosendahl, A.
Right arrow Articles by Sideras, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rosendahl, A.
Right arrow Articles by Sideras, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

International Immunology, Vol. 15, No. 12, pp. 1401-1414, December 2003
© 2003 Japanese Society for Immunology

Transforming growth factor-ß– and Activin–Smad signaling pathways are activated at distinct maturation stages of the thymopoeisis

Alexander Rosendahl1, Matthaios Speletas2, Karin Leandersson2, Fredrik Ivars2 and Paschalis Sideras1,3

1 AstraZeneca R & D Lund, Department of Bio & Molecular Sciences, Scheelevägen 2, 221 87 Lund, Sweden 2 Section for Immunology, BMC I:13, Lund University, 221 84 Lund, Sweden 3 Center of Transplantations, Foundation for Biomedical Research of the Academy of Athens, Soranou tou Efesiou 4, 10310 Athens, Greece

Correspondence to: A. Rosendahl; E-mail: alexander.rosendahl{at}astrazeneca.com
Transmitting editor: R. A. Flavell

Members of the transforming growth factor (TGF)-ß family play pivotal roles in the control of differentiation, proliferation and tolerance in peripheral T cells. Recently, they have been implicated in thymic selection, but their role is so far not well characterized. In the present study, we demonstrate that specific thymocyte populations are under the influence of either the TGF-ß and/or Activin pathway, and transduce signals into the nucleus via phosphorylated Smad2 (pSmad2). Thymocytes in the medulla and in the subcapsular zone expressed nuclear translocated pSmad2, a hallmark of active TGF-ß/Activin receptor signaling. When analyzed at the cellular level, the pSmad2+ cells were confined to the double-negative (DN) and single-positive (SP) subpopulations. Moreover, the most immature DN thymocytes (CD44+CD25 and CD44+CD25+) expressed higher levels of pSmad2 compared to the more mature DN. In vitro stimulation demonstrated that pure CD44+CD25, CD44+CD25+ and CD44+CD25+ thymocytes respond to ActivinA, while the mature CD4+ and CD8+ SP thymocytes respond to TGF-ß stimulation measured as enhanced phosphorylation of Smad2. Double staining of pSmad2+ cells with either the Activin type I receptor, ALK4, or the TGF-ß type I receptor, ALK5, demonstrated that pSmad2+ DN cells exhibited high levels of immunoreactivity to ALK4 and moderate levels of immunoreactivity to the TGF-ß-responsive ALK5 receptor. In sharp contrast, the SP pSmad2+ cells were predominately ALK5+. Collectively, our results demonstrate that early and late thymocytes express pSmad2 in the nuclei in vivo. The functional experiments in vitro suggest that members of the TGF-ß family (TGF-ß or Activin) may play important non-redundant roles during different stages of thymopoiesis.

Keywords: cytokine, cellular development and differentiation, TCR, thymus


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
BloodHome page
N. C. Robson, D. J. Phillips, T. McAlpine, A. Shin, S. Svobodova, T. Toy, V. Pillay, N. Kirkpatrick, D. Zanker, K. Wilson, et al.
Activin-A: a novel dendritic cell-derived cytokine that potently attenuates CD40 ligand-specific cytokine and chemokine production
Blood, March 1, 2008; 111(5): 2733 - 2743.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
R. Li, A. Rosendahl, G. Brodin, A. M. Cheng, A. Ahgren, C. Sundquist, S. Kulkarni, T. Pawson, C.-H. Heldin, and R. L. Heuchel
Deletion of Exon I of SMAD7 in Mice Results in Altered B Cell Responses.
J. Immunol., June 1, 2006; 176(11): 6777 - 6784.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
V. E. Mick, T. K. Starr, T. M. McCaughtry, L. K. McNeil, and K. A. Hogquist
The Regulated Expression of a Diverse Set of Genes during Thymocyte Positive Selection In Vivo
J. Immunol., November 1, 2004; 173(9): 5434 - 5444.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.