Helmholtz Centre for Infection Research, Viral Immune Modulation Research Group, Inhoffenstr. 7, 38124 Braunschweig, Germany.
Technische Universität Braunschweig, Institute of Genetics, Spielmannstr. 7, 38106 Braunschweig, Germany.
J Cell Sci. 2020 Apr 23;134(5):jcs246421. doi: 10.1242/jcs.246421.
Protein tyrosine phosphatase 1B (PTP1B, also known as PTPN1) is a negative regulator of the leptin and insulin signalling pathways. This phosphatase is of great interest as PTP1B-knockout mice are protected against the development of obesity and diabetes. Here, we provide evidence for a novel function of PTP1B that is independent of its phosphatase activity, but requires its localisation to the membrane of the endoplasmic reticulum. Upon activation of pattern recognition receptors, macrophages and plasmacytoid dendritic cells from PTP1B-knockout mice secrete lower amounts of type I interferon (IFN) than cells from wild-type mice. In contrast, secretion of the proinflammatory cytokines TNFα and IL6 was unaltered. While PTP1B deficiency did not affect transcription, type I IFN accumulated in macrophages, suggesting a role for PTP1B in mediating secretion of type I IFN. In summary, we have uncovered that PTP1B positively regulates the type I IFN response by promoting secretion of key antiviral cytokines.
蛋白酪氨酸磷酸酶 1B(PTP1B,也称为 PTPN1)是瘦素和胰岛素信号通路的负调节剂。这种磷酸酶非常有趣,因为 PTP1B 敲除小鼠可以预防肥胖和糖尿病的发生。在这里,我们提供了 PTP1B 的一个新功能的证据,该功能独立于其磷酸酶活性,但需要其定位于内质网的膜上。在模式识别受体被激活后,PTP1B 敲除小鼠的巨噬细胞和浆细胞样树突状细胞分泌的 I 型干扰素(IFN)比野生型小鼠的细胞少。相比之下,促炎细胞因子 TNFα 和 IL6 的分泌没有改变。虽然 PTP1B 缺乏并不影响转录,但 I 型 IFN 在巨噬细胞中积累,表明 PTP1B 在介导 I 型 IFN 的分泌中起作用。总之,我们发现 PTP1B 通过促进关键抗病毒细胞因子的分泌来正向调节 I 型 IFN 反应。