Laboratory of Cardiovascular Pharmacology, Department of Biopharmaceutical Sciences, Kobe Gakuin University Minatojima 1-1-3, Chuo-ku, Kobe, 650-8586, Japan.
Pharmacol Res Perspect. 2014 Apr;2(2):e00039. doi: 10.1002/prp2.39. Epub 2014 Apr 1.
Orthovanadate (OVA), a protein tyrosine phosphatase (PTPase) inhibitor, exerts contractile effects on smooth muscle in a Rho-kinase-dependent manner, but the precise mechanisms are not elucidated. The aim of this study was to determine the potential roles of Src and epidermal growth factor receptor (EGFR) in the OVA-induced contraction of rat aortas and the phosphorylation of myosin phosphatase target subunit 1 (MYPT1; an index of Rho-kinase activity) in vascular smooth muscle cells (VSMCs). Aortic contraction by OVA was significantly blocked not only by Rho kinase inhibitors Y-27632 [R-[+]-trans-N-[4-pyridyl]-4-[1-aminoethyl]-cyclohexanecarboxamide] and hydroxyfasudil [1-(1-hydroxy-5-isoquinolinesulfonyl)homopiperazine] but also by Src inhibitors PP2 [4-amino-3-(4-chlorophenyl)-1-(t-butyl)-1H-pyrazolo[3,4-d]pyrimidine] and Src inhibitor No. 5 [4-(3'-methoxy-6'-chloro-anilino)-6-methoxy-7(morpholino-3-propoxy)-quinazoline], and the EGFR inhibitors AG1478 [4-(3-chloroanilino)-6,7-dimethoxyquinazoline] and EGFR inhibitor 1 [cyclopropanecarboxylic acid-(3-(6-(3-trifluoromethyl-phenylamino)-pyrimidin-4-ylamino)-phenyl)-amide]. OVA induced rapid increases in the phosphorylation of MYPT1 (Thr-853), Src (Tyr-416), and EGFR (Tyr-1173) in VSMCs, and Src inhibitors abolished these effects. OVA-induced Src phosphorylation was abrogated by Src inhibitors, but not affected by inhibitors of EGFR and Rho-kinase. Inhibitors of Src and EGFR, but not Rho-kinase, also blocked OVA-induced EGFR phosphorylation. Furthermore, a metalloproteinase inhibitor TAPI-0 [N-(R)-[2-(hydroxyaminocarbonyl) methyl]-4-methylpentanoyl-l-naphthylalanyl-l-alanine amide] and an inhibitor of heparin-binding EGF (CRM 197) not only abrogated the OVA-induced aortic contraction, but also OVA-induced EGFR and MYPT1 phosphorylation, suggesting the involvement of EGFR transactivation. OVA also induced EGFR phosphorylation at Tyr-845, one of residues phosphorylated by Src. These results suggest that OVA-induced vasocontraction is mediated by the Rho-kinase-dependent inactivation of myosin light-chain phosphatase via signaling downstream of Src-induced transactivation of EGFR.
正钒酸钠(OVA)是一种蛋白酪氨酸磷酸酶(PTPase)抑制剂,它以依赖 Rho 激酶的方式对平滑肌产生收缩作用,但确切的机制尚不清楚。本研究旨在确定Src 和表皮生长因子受体(EGFR)在 OVA 诱导的大鼠主动脉收缩和血管平滑肌细胞(VSMCs)中肌球蛋白磷酸酶靶亚单位 1(MYPT1;Rho-激酶活性的指标)磷酸化中的潜在作用。OVA 引起的主动脉收缩不仅被 Rho 激酶抑制剂 Y-27632[R-[+]-反-N-[4-吡啶基]-4-[1-氨基乙基]-环己烷甲酰胺]和羟基法舒地尔[1-(1-羟基-5-异喹啉磺酰基)同哌嗪]阻断,也被 Src 抑制剂 PP2[4-氨基-3-(4-氯苯基)-1-(叔丁基)-1H-吡唑并[3,4-d]嘧啶]和 Src 抑制剂 No.5[4-(3'-甲氧基-6'-氯苯胺基)-6-甲氧基-7(吗啉-3-丙氧基)-喹唑啉]以及 EGFR 抑制剂 AG1478[4-(3-氯苯胺基)-6,7-二甲氧基喹唑啉]和 EGFR 抑制剂 1[环丙烷羧酸-(3-(6-(3-三氟甲基-苯氨基)-嘧啶-4-基氨基)-苯基)-酰胺]阻断。OVA 诱导 VSMCs 中 MYPT1(Thr-853)、Src(Tyr-416)和 EGFR(Tyr-1173)的磷酸化迅速增加,而 Src 抑制剂则消除了这些作用。Src 抑制剂消除了 OVA 诱导的 Src 磷酸化,但对 EGFR 和 Rho 激酶抑制剂无影响。Src 抑制剂也阻断了 OVA 诱导的 EGFR 磷酸化,但 EGFR 和 Rho 激酶抑制剂对其无影响。此外,基质金属蛋白酶抑制剂 TAPI-0[N-(R)-[2-(羟氨基羰基)甲基]-4-甲基戊酰基-L-萘基丙氨酰-L-丙氨酸酰胺]和肝素结合表皮生长因子(CRM 197)抑制剂不仅阻断了 OVA 诱导的主动脉收缩,还阻断了 OVA 诱导的 EGFR 和 MYPT1 磷酸化,表明 EGFR 转位激活的参与。OVA 还诱导 EGFR 在 Tyr-845 处磷酸化,这是 Src 磷酸化的一个残基。这些结果表明,OVA 诱导的血管收缩是通过 Src 诱导的 EGFR 转位激活下游信号转导,导致 Rho 激酶依赖性肌球蛋白轻链磷酸酶失活而介导的。