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n3:pmcid
PMC0
bibo:doi
10.1084%2Fjem.20092176
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_:vb6576549 _:vb6576553
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_:vb6576549
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dc:title
materials and methods
n5:contains
_:vb6576550 _:vb6576551 _:vb6576552
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_:vb6576550
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Fetal liver cells from E13.5 Nfil3−/− embryos were cultured in 20% FCS, 100 mg/ml mSlf, 250 mg/ml mFlt3L, and 50 ng/ml mTPO as previously described (Pellegrini et al., >>2005<<). The WT Nfil3 gene and Nfil3 lacking its DNA binding domain (synthesized using information provided by T.
n3:mentions
n2:15905188
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_:vb6576551
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IFN-γ production was assessed by intracellular flow cytometry (Prussin and Metcalfe, >>1995<<).
n3:mentions
n2:8551029
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_:vb6576552
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with 150 µg poly I:C 16 h before sacrifice, and NK cytotoxicity was analyzed in FACS-sorted NK1.1+CD3− splenocytes using a flow cytometric method as previously described (Souza et al., >>2001<<).
n3:mentions
n2:11334996
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_:vb6576553
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n5:Section
dc:title
results and discussion
n5:contains
_:vb6576554 _:vb6576555 _:vb6576556 _:vb6576557 _:vb6576558 _:vb6576559 _:vb6576560 _:vb6576561 _:vb6576562 _:vb6576563 _:vb6576564 _:vb6576565
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We created this animal by inserting an IRES β-geo cassette (Murakami et al., >>1997<<) into exon 2 of the Nfil3 gene (Fig.
n3:mentions
n2:9427541
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_:vb6576555
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Previous studies using in situ hybridization in mouse brain have demonstrated significant Nfil3 mRNA expression in the suprachiasmatic nucleus, hippocampus, gyrus dentatus, and piriform cortex (Mitsui et al., >>2001<<). In our hands, X-Gal staining of brain tissues from Nfil3+/−-IRES β-geo mice revealed a similar pattern of Nfil3 expression.
n3:mentions
n2:11316793
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_:vb6576556
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Murine multipotent progenitors (Kondo et al., >>1997<<) give rise to mNK cells in vitro after appropriate cytokine stimulation (Shimozato et al., 2002).
n3:mentions
n2:9393859
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_:vb6576557
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Murine multipotent progenitors (Kondo et al., 1997) give rise to mNK cells in vitro after appropriate cytokine stimulation (Shimozato et al., >>2002<<). We applied an in vitro NK cell generation assay to a lineage-negative (Lin−) population of BM cells.
n3:mentions
n2:11823506
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_:vb6576558
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According to the current literature (Kim et al., >>2002<<; Vosshenrich et al., 2005; Di Santo, 2006; Huntington et al., 2007; for review see Boos et al., 2008), the development of NK lineage cells (CD122+NKG2D+ BM cells) progresses through three major stages defined by NK1.1 and DX5 expression:
n3:mentions
n2:12006976
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_:vb6576559
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According to the current literature (Kim et al., 2002; Vosshenrich et al., >>2005<<; Di Santo, 2006; Huntington et al., 2007; for review see Boos et al., 2008), the development of NK lineage cells (CD122+NKG2D+ BM cells) progresses through three major stages defined by NK1.1 and DX5 expression:
n3:mentions
n2:15766674
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_:vb6576560
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n3:Context
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According to the current literature (Kim et al., 2002; Vosshenrich et al., 2005; Di Santo, >>2006<<; Huntington et al., 2007; for review see Boos et al., 2008), the development of NK lineage cells (CD122+NKG2D+ BM cells) progresses through three major stages defined by NK1.1 and DX5 expression:
n3:mentions
n2:16551250
Subject Item
_:vb6576561
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n3:Context
rdf:value
According to the current literature (Kim et al., 2002; Vosshenrich et al., 2005; Di Santo, 2006; Huntington et al., >>2007<<; for review see Boos et al., 2008), the development of NK lineage cells (CD122+NKG2D+ BM cells) progresses through three major stages defined by NK1.1 and DX5 expression:
n3:mentions
n2:17717540
Subject Item
_:vb6576562
rdf:type
n3:Context
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According to the current literature (Kim et al., 2002; Vosshenrich et al., 2005; Di Santo, 2006; Huntington et al., 2007; for review see Boos et al., >>2008<<), the development of NK lineage cells (CD122+NKG2D+ BM cells) progresses through three major stages defined by NK1.1 and DX5 expression:
n3:mentions
n2:18266115
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_:vb6576563
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Like the work of Gascoyne et al. (>>2009<<), our study demonstrates that mNK cells are markedly reduced in number, maturity, and functional capability in the absence of Nfil3 but that other hematopoietic cell lineages are not adversely affected.
n3:mentions
n2:19749763
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The results of such studies may be highly significant, especially given the importance of NKG2D in immune surveillance (Guerra et al., >>2008<<).
n3:mentions
n2:18394936
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_:vb6576565
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Further studies designed to identify the target genes regulated by Nfil3 in NK cells, either in an Id2-dependent or -independent fashion (Gascoyne et al., >>2009<<), will help to elucidate the molecular pathways underlying the development and survival of NK cells.
n3:mentions
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