Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC 20007, USA.
Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC 20007, USA.
Cell Signal. 2018 Dec;52:147-154. doi: 10.1016/j.cellsig.2018.09.005. Epub 2018 Sep 10.
Extracellular signal-regulated kinase (ERK), also known as classical mitogen-activated protein kinase, plays critical roles in cell regulation. ERK is activated through phosphorylation by a cascade of protein kinases including MEK. Various ligands activate the MEK/ERK pathway through receptor-dependent cell signaling. In cultured cells, many ligands such as growth factors, hormones, cytokines and vasoactive peptides elicit transient activation of MEK/ERK, often peaking at ~10 min after the cell treatment. Here, we describe a novel biological event, in which ligand-mediated cell signaling results in the dephosphorylation of MEK/ERK. Neuromedin N and neurotensin, peptides derived from the same precursor polypeptide, elicit cell signaling through the neurotensin receptors. In cultured human pulmonary artery smooth muscle cells (PASMCs), but not in human pulmonary artery endothelial cells (PAECs), we found that both neuromedin N and neurotensin promoted the dephosphorylation of ERK and MEK. Human PASMCs were found to express neurotensin receptor (NTR)-1, -2 and -3, while human PAECs only express NTR3. Neuromedin N-mediated dephosphorylation was suppressed by small chemical inhibitors of protein phosphatase 1/2A and peptidyl-prolyl isomerase. Transmission electron microscopy showed the formation of endocytic vesicles in response to neuromedin N treatment, and dephosphorylation did not occur when sorting nexin 9, a critical regulator of the endocytic vesicle formation, was knocked down. We conclude that neuromedin N and neurotensin elicit a unique dephosphorylation signaling in the MEK/ERK pathway that is regulated by endocytosis. Considering the pathophysiological importance of the MEK/ERK pathway, this discovery of the dephosphorylation mechanism should advance the field of cell signaling.
细胞外信号调节激酶(ERK),也称为经典丝裂原活化蛋白激酶,在细胞调节中发挥关键作用。ERK 通过包括 MEK 在内的一系列蛋白激酶的磷酸化而被激活。各种配体通过受体依赖性细胞信号转导激活 MEK/ERK 途径。在培养的细胞中,许多配体,如生长因子、激素、细胞因子和血管活性肽,会引发 MEK/ERK 的短暂激活,通常在细胞处理后约 10 分钟达到峰值。在这里,我们描述了一种新的生物学事件,即配体介导的细胞信号转导导致 MEK/ERK 的去磷酸化。神经肽 N 和神经降压素是同一前体多肽衍生的肽,通过神经降压素受体引发细胞信号转导。在培养的人肺动脉平滑肌细胞(PASMCs)中,但不在人肺动脉内皮细胞(PAECs)中,我们发现神经肽 N 和神经降压素都促进 ERK 和 MEK 的去磷酸化。人 PASMCs 表达神经降压素受体(NTR)-1、-2 和 -3,而人 PAECs 仅表达 NTR3。神经肽 N 介导的去磷酸化被蛋白磷酸酶 1/2A 和肽基脯氨酰顺反异构酶的小分子化学抑制剂抑制。透射电子显微镜显示,神经肽 N 处理后形成内吞小泡,当关键内吞小泡形成调节因子分选连接蛋白 9 被敲低时,去磷酸化不会发生。我们得出结论,神经肽 N 和神经降压素在 MEK/ERK 途径中引发一种独特的去磷酸化信号,该信号受内吞作用调节。考虑到 MEK/ERK 途径的病理生理学重要性,这种去磷酸化机制的发现应该会推动细胞信号转导领域的发展。