NF-κB is dispensable for normal lymphocyte development in bone marrow but required for protection of progenitors from TNFα
Author(s) -
Hideya Igarashi,
Yoshihiro Baba,
Yoshinori Nagai,
Eijiro Jimi,
Sankar Ghosh,
Paul W. Kincade
Publication year - 2006
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/dxl002
Subject(s) - bone marrow , progenitor cell , immunology , tumor necrosis factor alpha , nf κb , progenitor , lymphocyte , haematopoiesis , cancer research , microbiology and biotechnology , biology , inflammation , medicine , stem cell
Levels of the nuclear factor-kappa B (NF-kappaB)/Rel family of proteins are carefully modulated in differentiating lymphocytes, where these transcription factors are thought to be important for survival and fate decisions. In contrast, gene-targeting experiments have not revealed clear roles for these transcription factors in lymphopoiesis within bone marrow. Inhibition of NF-kappaB by introduction of mutated I kappa B alpha, a 'superinhibitor' of NF-kappaB, into hematopoietic stem cells or early progenitors suppressed B as well as T lymphopoiesis following transplantation into immunodeficient mice. Furthermore, a NF-kappaB essential modifier-binding domain (NBD) peptide that blocks IKB kinase (IKK) activity selectively impaired the generation of adult B lineage cells. However, this suppression did not occur when a neutralizing antibody to tumor necrosis factor alpha (TNFalpha) was added to the cultures, or in circumstances where few non-lymphoid cells were present. We conclude that while NF-kappaB plays a survival-promoting role in lymphoid progenitors, this may only be significant in circumstances such as transplantation when levels of TNFalpha are high.
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