Abstract
The prevailing model for adult hematopoiesis postulates that the first lineage commitment step results in a strict separation of common myeloid and common lymphoid pathways. However, the recent identification of granulocyte/monocyte (GM)-lymphoid restricted lymphoid-primed multipotent progenitors (LMPPs) and primitive common myeloid progenitors (CMPs) within the "HSC" compartment provide compelling support for establishment of independent GM-megakaryocyte/erythroid (GM-MkE) and GM-lymphoid commitment pathways as decisive early lineage fate decisions. These changes in lineage potentials are corroborated by corresponding changes in multilineage transcriptional priming, as LMPPs down-regulate MkE priming but become GM-lymphoid transcriptionally primed, whereas CMPs are GM-MkE primed. These distinct biological and molecular relationships are established already in the fetal liver.
Originalsprog | Engelsk |
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Tidsskrift | Seminars in Immunology |
Vol/bind | 20 |
Udgave nummer | 4 |
Sider (fra-til) | 213-20 |
Antal sider | 8 |
ISSN | 1044-5323 |
DOI | |
Status | Udgivet - aug. 2008 |
Udgivet eksternt | Ja |