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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 
 
 

Failure of lymphopoiesis after adoptive transfer of NF-kappaB-deficient fetal liver cells.

Mice deficient in the p65 subunit of NF-kappaB die during fetal development. Introduction of p50/ p65-deficient fetal liver cells into lethally irradiated hosts resulted in a severe deficit of fetal liver-derived lymphocytes and their immediate precursors but an overabundance of fetal liver-derived granulocytes. Surprisingly, simultaneous transplantation of wild-type bone marrow cells rescued the production of p50/ p65-deficient lymphocytes. Expression of immunoglobulin K light chains on these rescued NF-kappaB-deficient B lymphocytes was normal. These results suggest that while p50 and p65 do not regulate the maturation of pre-B cells, NF-kappaB mediates the development or survival of an early lymphocyte precursor through regulation of an extracellular factor.[1]

References

  1. Failure of lymphopoiesis after adoptive transfer of NF-kappaB-deficient fetal liver cells. Horwitz, B.H., Scott, M.L., Cherry, S.R., Bronson, R.T., Baltimore, D. Immunity (1997) [Pubmed]
 
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