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Protein tyrosine phosphatase PTPN21 acts as a negative regulator of ICAM-1 by dephosphorylating IKKβ in TNF-α-stimulated human keratinocytes

机译:蛋白酪氨酸磷酸酶PTPN21通过使TNF-α刺激的人角质形成细胞中的IKKβ去磷酸化而成为ICAM-1的负调节剂

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摘要

Intercellular adhesion molecule-1 (ICAM-1), which is induced by tumor necrosis factor (TNF)-α, contributes to the entry of immune cells into the site of inflammation in the skin. Here, we show that protein tyrosine phosphatase non-receptor type 21 (PTPN21) negatively regulates ICAM-1 expression in human keratinocytes. PTPN21 expression was transiently induced after stimulation with TNF-α. When overexpressed, PTPN21 inhibited the expression of ICAM-1 in HaCaT cells but PTPN21 C1108S, a phosphatase activity-inactive mutant, failed to inhibit ICAM-1 expression. Nuclear factor-κB (NF-κB), a key transcription factor of ICAM-1 gene expression, was inhibited by PTPN21, but not by PTPN21 C1108S. PTPN21 directly dephosphorylated phospho-inhibitor of κB (IκB)-kinase β (IKKβ) at Ser177/181. This dephosphorylation led to the stabilization of IκBα and inhibition of NF-κB activity. Taken together, our results suggest that PTPN21 could be a valuable molecular target for regulation of inflammation in the skin by dephosphorylating p-IKKβ and inhibiting NF-κB signaling.
机译:由肿瘤坏死因子(TNF)-α诱导的细胞间粘附分子-1(ICAM-1)有助于免疫细胞进入皮肤炎症部位。在这里,我们显示蛋白质酪氨酸磷酸酶非受体21型(PTPN21)负调控人类角质形成细胞中的ICAM-1表达。在用TNF-α刺激后瞬时诱导PTPN21表达。当过表达时,PTPN21抑制HaCaT细胞中ICAM-1的表达,但是PTPN21 C1108S(一种磷酸酶活性失活的突变体)未能抑制ICAM-1的表达。核因子-κB(NF-κB)是ICAM-1基因表达的关键转录因子,其受PTPN21抑制,但不受PTPN21 C1108S抑制。 PTPN21在Ser177 / 181处直接使κB(IκB)激酶β(IKKβ)的磷酸化抑制剂去磷酸化。这种去磷酸化导致IκBα的稳定和NF-κB活性的抑制。两者合计,我们的结果表明PTPN21可能是通过调节p-IKKβ磷酸化和抑制NF-κB信号传导来调节皮肤炎症的有价值的分子靶标。

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