The pre-T Cell Receptor (pre-TCR) is a receptor expressed early during the development of T cells in the thymus. It's signaling is essential for the maturation of T cells as it induces proliferation and differentiation through downstream signaling pathways that involve the activation of key transcription factors. One of the main functions of the pre-TCR is the induction of cell survival as cells unable to express the receptor die by programmed cell death. However, the mechanisms of both apoptotic death of pre-TCR non-expressing thymocytes and the pre-TCR mediated survival are poorly understood. In this proposal we attempt to identify the molecular mechanisms responsible for the induction of survival and study the role of well-characterized death inducers in the apoptotic cascades of pre-T cells. To achieve that we a) analyze biochemically the constituents of the apoptotic pathway in these cells, b) study thymic phenotypes of mice deficient for several genes - key components of the apoptotic machinery, and c) characterize the nature of pre-TCR derived antiapoptotic signals and in particular the expression pattern and the function of the pre-TCR-induced prosurvival factor A1 and the pre-TCR-suppressed pro-apoptotic Bim. We are also linking constitutive pre-TCR signaling, that leads to deregulated survival and proliferation, to the induction of T cell acute lymphoblastic leukemia (T-ALL). To study the role of the pre-TCR in thymocytes transformation we will a) address the nature of interactions of oncogenes (Notch) with pre-TCR signaling, b) study the significance of pre-TCR gene-targets in the triggering of transformation and c) attempt to identify additional genetic events contributing in the establisment of the disease. The proposed experiments will help to identify the molecular mechanisms regulating pre-T cell survival and death and pinpoint pre-TCR-induced signaling pathways responsible for the malignant transformation of thymocytes.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA105129-02
Application #
7057796
Study Section
Cellular and Molecular Immunology - B (CMI)
Program Officer
Mccarthy, Susan A
Project Start
2005-05-01
Project End
2006-11-01
Budget Start
2006-05-01
Budget End
2006-11-01
Support Year
2
Fiscal Year
2006
Total Cost
$294,110
Indirect Cost
Name
University of Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Kourtis, Nikos; Lazaris, Charalampos; Hockemeyer, Kathryn et al. (2018) Oncogenic hijacking of the stress response machinery in T cell acute lymphoblastic leukemia. Nat Med 24:1157-1166
Aranda-Orgilles, Beatriz; SaldaƱa-Meyer, Ricardo; Wang, Eric et al. (2016) MED12 Regulates HSC-Specific Enhancers Independently of Mediator Kinase Activity to Control Hematopoiesis. Cell Stem Cell 19:784-799
Ntziachristos, Panagiotis; Abdel-Wahab, Omar; Aifantis, Iannis (2016) Emerging concepts of epigenetic dysregulation in hematological malignancies. Nat Immunol 17:1016-24
Strikoudis, Alexandros; Lazaris, Charalampos; Trimarchi, Thomas et al. (2016) Regulation of transcriptional elongation in pluripotency and cell differentiation by the PHD-finger protein Phf5a. Nat Cell Biol 18:1127-1138
Guillamot, Maria; Cimmino, Luisa; Aifantis, Iannis (2016) The Impact of DNA Methylation in Hematopoietic Malignancies. Trends Cancer 2:70-83
King, Bryan; Boccalatte, Francesco; Moran-Crusio, Kelly et al. (2016) The ubiquitin ligase Huwe1 regulates the maintenance and lymphoid commitment of hematopoietic stem cells. Nat Immunol 17:1312-1321
Gao, Jie; Buckley, Shannon M; Cimmino, Luisa et al. (2015) The CUL4-DDB1 ubiquitin ligase complex controls adult and embryonic stem cell differentiation and homeostasis. Elife 4:
Trimarchi, Thomas; Aifantis, Iannis (2015) The pre-BCR to the rescue: therapeutic targeting of pre-B cell ALL. Cancer Cell 27:321-3
Witkowski, M T; Cimmino, L; Hu, Y et al. (2015) Activated Notch counteracts Ikaros tumor suppression in mouse and human T-cell acute lymphoblastic leukemia. Leukemia 29:1301-11
Pitt, Lauren A; Tikhonova, Anastasia N; Hu, Hai et al. (2015) CXCL12-Producing Vascular Endothelial Niches Control Acute T Cell Leukemia Maintenance. Cancer Cell 27:755-68

Showing the most recent 10 out of 70 publications