首页> 外文期刊>FEBS Letters >Hematopoietic cell‐specific adapter proteins, SLP‐76 and BLNK, effectively activate NF‐AT as well as NF‐κB by Syk and Tec PTKs in non‐lymphoid cell lines
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Hematopoietic cell‐specific adapter proteins, SLP‐76 and BLNK, effectively activate NF‐AT as well as NF‐κB by Syk and Tec PTKs in non‐lymphoid cell lines

机译:造血细胞特异性衔接蛋白SLP-76和BLNK通过Syk和Tec PTK在非淋巴细胞系中有效激活NF-AT和NF-κB

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>To investigate the roles of various hematopoietic cell-specific adapter proteins in T cell receptor (TCR)-signaling leading to nuclear factor of activated T cell (NF-AT) and nuclear factor of κB (NF-κB) activation, we reconstituted TCR-signaling with CD8/ζ, various protein tyrosine kinases (PTKs), and adapter proteins in a non-lymphoid cell line, 293T. We show that SLP-76 and BLNK, but not LAT, effectively co-operated with Syk and Tec family PTKs to activate NF-AT and NF-κB. We also show that Tec family PTKs enhanced endogenous phospholipase C (PLC)-γ1 phosphorylation induced by CD8/ζ and Syk in 293T cells. These results imply that PLC-γ1 may play a critical role in a hematopoietic cell-specific adapter protein-mediated NF-AT and NF-κB activation in a non-lymphoid cell.
机译:>要研究各种造血细胞特异性衔接蛋白在T细胞受体(TCR)信号转导导致活化T细胞核因子(NF-AT)和κB核因子(NF-κB)活化的作用,我们在非淋巴细胞系293T中用CD8 /ζ,各种蛋白酪氨酸激酶(PTK)和衔接子蛋白重建TCR信号。我们显示SLP-76和BLNK,但不是LAT,与Syk和Tec家族的PTK有效地协同激活了NF-AT和NF-κB。我们还显示,Tec家族PTK增强了293T细胞中CD8 /ζ和Syk诱导的内源性磷脂酶C(PLC)-γ1磷酸化。这些结果暗示PLC-γ1可能在非淋巴细胞中在造血细胞特异性衔接蛋白介导的NF-AT和NF-κB活化中起关键作用。

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