Olschewski Daniel Navin, Hofschröer Verena, Nielsen Nikolaj, Seidler Daniela G, Schwab Albrecht, Stock Christian
Institute of Physiology II, University of Münster, Münster, Germany.
Department of Gastroenterology, Hannover Medical School, Hannover, Germany.
Cell Physiol Biochem. 2018;45(6):2560-2576. doi: 10.1159/000488274. Epub 2018 Mar 16.
BACKGROUND/AIMS: The peptide hormone angiotensin II (ATII) plays a prominent role in regulating vasoconstriction and blood pressure. Its primary target is the angiotensin II receptor type 1 (AT1), the stimulation of which induces an increase in cytosolic [Ca2+] and calmodulin activation. Ca2+-bound (activated) calmodulin stimulates the activity of the Na+/ H+ exchanger isoform 1 (NHE1); and increased NHE1 activity is known to promote melanoma cell motility. The competitive AT1 receptor inhibitor losartan is often used to lower blood pressure in hypertensive patients. Since AT1 mediates ATII-stimulated NHE1 activity, we set out to investigate whether ATII and losartan have an impact on NHE1-dependent behavior of human melanoma (MV3) cells.
ATII receptor expression was verified by PCR, F-actin was visualized using fluorescently labeled phalloidin, and cytosolic [Ca2+] and pH were determined ratiometrically using Fura-2 and BCECF, respectively. MV3 cell behavior was analyzed using migration, adhesion, invasion and proliferation assays.
MV3 cells express both AT1 and the angiotensin II receptor type 2 (AT2). Stimulation of MV3 cells with ATII increased NHE1 activity which could be counteracted by both losartan and the Ca2+/ calmodulin inhibitor ophiobolin-A. ATII stimulation induced a decrease in MV3 cell migration and a more spherical cell morphology accompanied by an increase in the density of F-actin. Independently of the presence of ATII, both NHE1 and migratory activity were reduced when AT1 was blocked by losartan. On the other hand, losartan clearly increased cell adhesion to, and the invasion of, a collagen type I substrate. The AT2 inhibitor PD123319 did not affect NHE1 activity, proliferation and migration, but increased adhesion and invasion.
Losartan inhibits NHE1 activity and the migration of human melanoma cells. At the same time, losartan promotes MV3 cell adhesion and invasion. The therapeutic use of AT1 antagonists (sartans) in hypertensive cancer patients should therefore be given critical consideration.
背景/目的:肽激素血管紧张素II(ATII)在调节血管收缩和血压方面发挥着重要作用。其主要靶点是1型血管紧张素II受体(AT1),刺激该受体可导致胞质[Ca2+]增加和钙调蛋白激活。与Ca2+结合(激活)的钙调蛋白可刺激1型钠/氢交换体(NHE1)的活性;已知NHE1活性增加会促进黑色素瘤细胞的运动。竞争性AT1受体抑制剂氯沙坦常用于降低高血压患者的血压。由于AT1介导ATII刺激的NHE1活性,我们着手研究ATII和氯沙坦是否对人黑色素瘤(MV3)细胞的NHE1依赖性行为有影响。
通过PCR验证ATII受体表达,使用荧光标记的鬼笔环肽观察F-肌动蛋白,分别使用Fura-2和BCECF通过比率法测定胞质[Ca2+]和pH。使用迁移、黏附、侵袭和增殖试验分析MV3细胞行为。
MV3细胞同时表达AT1和2型血管紧张素II受体(AT2)。用ATII刺激MV3细胞会增加NHE1活性,氯沙坦和Ca2+/钙调蛋白抑制剂蛇孢菌素-A均可抵消这种增加。ATII刺激导致MV3细胞迁移减少,细胞形态更呈球形,同时F-肌动蛋白密度增加。无论是否存在ATII,当氯沙坦阻断AT1时,NHE1和迁移活性均降低。另一方面,氯沙坦明显增加了细胞对I型胶原底物的黏附及侵袭。AT2抑制剂PD123319不影响NHE1活性、增殖和迁移,但增加了黏附和侵袭。
氯沙坦抑制人黑色素瘤细胞的NHE1活性和迁移。同时,氯沙坦促进MV3细胞的黏附和侵袭。因此,对于高血压癌症患者,应慎重考虑使用AT1拮抗剂(沙坦类药物)进行治疗。