Skip to main content
. 2011 May 22;1(1):34–45.

Table 1.

Transcription factors involved in NK cell development as determined by mouse knockout models

Transcription Factor Phenotype of Knockout Mouse References
Commitment
Ets-1 Decrease in NK cell numbers [23]
Impaired NKcell mediated cytotoxicity and IFN-γ secretion
PU.1* Reduced production of NKPs and mNKs [26]
Altered expression of receptors involved in development
Defective proliferation in response to cytokines
Maturation
STAT5 Developmental block at the NKP-iNK stage resulting in diminished [31-33]
E4BP4 NK cell numbers
Decrease in iNK cell numbers [35]
Almost undetectable mNK cells
Impaired NK cell mediated cytotoxicity
Id2 Decrease in mNK cell numbers [36]
Functional Maturation
MEF Decrease in NK cell numbers [39]
Impaired NK cell mediated cytotoxicity and IFN-γ secretion
Defective perforin expression
T-bet Decrease in NK cell numbers [40]
NK cells appear immature
Impaired NK cell mediated cytotoxicity and IFN-γ secretion
BLIMP1 Decrease in peripheral mNK cell numbers [42]
Decrease in Granzyme B expression
*

PU.1-/- mice die embryonically, therefore the role of PU.1 in NK development was determined by transfer of PU.1-/- fetal liver hematopoietic stem cells to Rag1-/-γc-/- mice. NK: Natural Killer; NKP: NK progenitors; iNK: immature NK; mNK: mature NK; IFN-γ: interferon-γ STAT: signal transducer and activator of transcription; MEF: myeloid ELF1 (E74-like factor 1)-like factor