» Articles » PMID: 16397133

Notch-dependent T-lineage Commitment Occurs at Extrathymic Sites Following Bone Marrow Transplantation

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2006 Jan 7
PMID 16397133
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

Early T-lineage progenitors (ETPs) arise after colonization of the thymus by multipotent bone marrow progenitors. ETPs likely serve as physiologic progenitors of T-cell development in adult mice, although alternative T-cell differentiation pathways may exist. While we were investigating mechanisms of T-cell reconstitution after bone marrow transplantation (BMT), we found that efficient donor-derived thymopoiesis occurred before the pool of ETPs had been replenished. Simultaneously, T lineage-restricted progenitors were generated at extrathymic sites, both in the spleen and in peripheral lymph nodes, but not in the bone marrow or liver. The generation of these T lineage-committed cells occurred through a Notch-dependent differentiation process. Multipotent bone marrow progenitors efficiently gave rise to extrathymic T lineage-committed cells, whereas common lymphoid progenitors did not. Our data show plasticity of T-lineage commitment sites in the post-BMT environment and indicate that Notch-driven extrathymic Tlineage commitment from multipotent progenitors may contribute to early T-lineage reconstitution after BMT.

Citing Articles

Cells and signals of the leukemic microenvironment that support progression of T-cell acute lymphoblastic leukemia (T-ALL).

Lyu A, Nam S, Humphrey R, Horton T, Ehrlich L Exp Mol Med. 2024; 56(11):2337-2347.

PMID: 39482533 PMC: 11612169. DOI: 10.1038/s12276-024-01335-7.


Notch pathway mutants do not equivalently perturb mouse embryonic retinal development.

Bosze B, Suarez-Navarro J, Cajias I, Brzezinski Iv J, Brown N PLoS Genet. 2023; 19(9):e1010928.

PMID: 37751417 PMC: 10522021. DOI: 10.1371/journal.pgen.1010928.


Cdc73 protects Notch-induced T-cell leukemia cells from DNA damage and mitochondrial stress.

Melnick A, Mullin C, Lin K, McCarter A, Liang S, Liu Y Blood. 2023; 142(25):2159-2174.

PMID: 37616559 PMC: 10733839. DOI: 10.1182/blood.2023020144.


DLBCL-associated NOTCH2 mutations escape ubiquitin-dependent degradation and promote chemoresistance.

Zhou N, Choi J, Grothusen G, Kim B, Ren D, Cao Z Blood. 2023; 142(11):973-988.

PMID: 37235754 PMC: 10656726. DOI: 10.1182/blood.2022018752.


A lineage-specific requirement for YY1 Polycomb Group protein function in early T cell development.

Assumpcao A, Fu G, Singh D, Lu Z, Kuehnl A, Welch R Development. 2021; 148(7).

PMID: 33766932 PMC: 8077518. DOI: 10.1242/dev.197319.


References
1.
Dejbakhsh-Jones S, Strober S . Identification of an early T cell progenitor for a pathway of T cell maturation in the bone marrow. Proc Natl Acad Sci U S A. 1999; 96(25):14493-8. PMC: 24464. DOI: 10.1073/pnas.96.25.14493. View

2.
Antin J, Weinberg D, Rappeport J . Evidence that pluripotential stem cells form splenic colonies in humans after marrow transplantation. Transplantation. 1985; 39(1):102-5. View

3.
Izon D, Aster J, He Y, Weng A, Karnell F, Patriub V . Deltex1 redirects lymphoid progenitors to the B cell lineage by antagonizing Notch1. Immunity. 2002; 16(2):231-43. DOI: 10.1016/s1074-7613(02)00271-6. View

4.
Katsura Y . Redefinition of lymphoid progenitors. Nat Rev Immunol. 2002; 2(2):127-32. DOI: 10.1038/nri721. View

5.
Lancrin C, Schneider E, Lambolez F, Arcangeli M, Garcia-Cordier C, Rocha B . Major T cell progenitor activity in bone marrow-derived spleen colonies. J Exp Med. 2002; 195(7):919-29. PMC: 2193723. DOI: 10.1084/jem.20011475. View