RhoH is important for positive thymocyte selection and T-cell receptor signaling

被引:63
作者
Dorn, Tatjana
Kuhn, Ursula
Bungartz, Gerd
Stiller, Sebastian
Bauer, Martina
Ellwart, Joachim
Peters, Thorsten
Scharffetter-Kochanek, Karin
Semmrich, Monika
Laschinger, Melanie
Holzmann, Bernhard
Klinkert, Wolfgang E. F.
Straten, Per Thor
Kollgaard, Tania
Sixt, Michael
Brakebusch, Cord
机构
[1] Univ Copenhagen, Dept Mol Pathol, DK-2100 Copenhagen, Denmark
[2] Max Planck Inst Biochem, Heisenberg Grp Regulat Cytoskeletal Org, D-82152 Martinsried, Germany
[3] Max Planck Inst Biochem, Dept Mol Med, Martinsried, Germany
[4] GSF Munich, Inst Mol Immunol, Munich, Germany
[5] Univ Ulm, Clin Dermatol & Allergol, Ulm, Germany
[6] Tech Univ Munich, Dept Surg, D-8000 Munich, Germany
[7] Max Planck Inst Neurobiol, Dept Neuroimmunol, Martinsried, Germany
[8] Herlev Univ Hosp, Dept Hematol, Ctr Canc Immunotherapy, DK-2730 Herlev, Denmark
关键词
D O I
10.1182/BLOOD-2006-04-019034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
RhoH is a small GTPase expressed only in the hematopoletic system. With the use of mice with targeted disruption of the RhoH gene, we demonstrated that RhoH is crucial for thymocyte maturation during DN3 to DN4 transition and during positive selection. Furthermore, the differentiation and expansion of DN3 and DN4 thymocytes in vitro were severely impaired. These defects corresponded to defective TCR signaling. Although RhoH is not required for TCR-induced activation of ZAP70 and ZAP70-mediated activation of p38, it is crucial for the tyrosine phosphorylation of LAT, PLC gamma 1, and Vav1 and for the activation of Erk and calcium influx. These data suggest that RhoH is important for pre-TCR and TCR signaling because it allows the efficient interaction of ZAP70 with the LAT signalosome, thus regulating thymocyte development.
引用
收藏
页码:2346 / 2355
页数:10
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