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Lymphoid Priming in Human Bone Marrow Begins Prior to CD10 Expression with Up-Regulation of L-selectin

The expression of CD10 has long been used to define human lymphoid commitment. We report a unique lymphoid-primed population in human bone marrow that was generated from hematopoietic stem cells (HSCs) before the onset of CD10 expression and B cell commitment. This subset was identified by high expr...

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Detalles Bibliográficos
Autores principales: Kohn, Lisa A., Hao, Qian-Lin, Sasidharan, Rajkumar, Parekh, Chintan, Ge, Shundi, Zhu, Yuhua, Mikkola, Hanna K.A., Crooks, Gay M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448017/
https://www.ncbi.nlm.nih.gov/pubmed/22941246
http://dx.doi.org/10.1038/ni.2405
Descripción
Sumario:The expression of CD10 has long been used to define human lymphoid commitment. We report a unique lymphoid-primed population in human bone marrow that was generated from hematopoietic stem cells (HSCs) before the onset of CD10 expression and B cell commitment. This subset was identified by high expression of the homing molecule L-selectin (CD62L). CD10(−)CD62L(hi) progenitors possessed full lymphoid and monocytic potential, but lacked erythroid potential. Gene expression profiling placed the CD10(−)CD62L(hi) population at an intermediate stage of differentiation between HSCs and lineage-negative (Lin(−)) CD34(+)CD10(+) progenitors. L-selectin was expressed on immature thymocytes and its ligands were expressed at the cortico-medullary junction, suggesting a possible role in thymic homing. These studies identify the earliest stage of lymphoid priming in human bone marrow.