Change of angiotensin-converting enzyme 2 expression in the macrophage foam cell induced by oxidized low density lipoprptein

Acta Anatomica Sinica ›› 2016, Vol. 47 ›› Issue (1) : 42-48.

Welcome to visit Acta Anatomica Sinica! Today is Chinese
Acta Anatomica Sinica ›› 2016, Vol. 47 ›› Issue (1) : 42-48.
cell and molecules biology

Change of angiotensin-converting enzyme 2 expression in the macrophage foam cell induced by oxidized low density lipoprptein

Author information +
History +

Abstract

Objective To investigate the change of ACE2 expression in the macrophage foam cell induced by ox-LDL. Methods Different concentrations of ox-LDL were used to induce macrophage cell RAW264.7 into foam cells, the intracellular lipid droplets amounts were observed by oil red O staining, the content of MDA was measured to identify oxidative damage, Real-Time PCR was used to detect ACE2 and MAS mRNA expression, the activity of SOD and the content of GSH were measured by chemocolorimetry. Results The macrophages became larger and rounder after treated by ox-LDL (20、40、60、80μg·ml-1) for 24h by oil red O staining, the amount of lipid droplets in the cytoplasm increased in a dose-dependent manner. The MDA content was increased significantly compare with the control group using 60μg·ml-1 ox-LDL treatment (P<0.01), Real-time PCR results showed that ACE2 and MAS mRNA expression in model group were decreased (P<0.05), and the SOD activity and the GSH content were also decreased (P<0.01 or P<0.05) significantly in model group. Conclusion Macrophage foam cell formation is closely related with the down-regulation of ACE2 and MAS expression, and that means ACE2 has anti-oxidative effect which may be related to SOD and GSH.

Key words

ox-LDL / Macrophage / Foam cell / ACE2 / Anti-oxidative effect

Cite this article

Download Citations
Change of angiotensin-converting enzyme 2 expression in the macrophage foam cell induced by oxidized low density lipoprptein[J]. Acta Anatomica Sinica. 2016, 47(1): 42-48

References

[1] Takahashi K, Takeya M, Sakashita N. Multifunctional roles of macrophages in the development and progression of atherosclerosis in humans and experimental animals[J]. Med Electron Microsc, 2002; 35(4): 179-203.
[2] Brasier AR,?Recinos A 3rd,?Eledrisi MS. Vascular inflammation and the rennin-angiotensin system[J]. Arterioscler Thromb Vasc Biol, 2002; 22(8):1257-1266.
[3] Donoghue M, Hsieh F, Baronas E, et al. A novel angiotensin-converting enzyme-related carboxypeptidase (ACE2) converts angiotensin I to angiotensin 1-9[J]. Circ Res, 2000; 87(5): E1-9.
[4] Sluimer JC, Gasc JM, Hamming I, et al. Angiotensin-converting enzyme 2 (ACE2) expression and activity in human carotid atherosclerotic lesions[J]. Pathology, 2008; 215(5):273-279.
[5] Tikellis C, Bernardi S, Burns WC. Angiotensin-converting enzyme 2 is a key modulator of the rennin- angiotensin system in cardiovascular and renal disease[J]. Curr Opin Nephrol Hypertens, 2011; 20(1): 62-68.
[6] Peltonena T, N?p?nkangas J, Ohtonen P, et al. (Pro)renin receptors and angiotensin converting enzyme 2/angiotensin-(1-7)/Mas receptor axis in human aortic valve stenosis[J]. Atherosclerosis, 2011; 216(1): 35-43.
[7] Santos RA, Simoes e Silva AC, Maric C, et al. Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas[J]. Proc Natl Acad Sci USA, 2003; 100(14):8258-8263.
[8] 唐颖, 倪兵, 陈代杰. 巨噬细胞泡沫化抑制剂的研究进展[J].中国新药与临床杂志, 2005; 24(11): 903-905.
[9] Kita T,Kume N, Minami M, et al. Role of oxidized LDL in atherosclerosis[J]. Ann N Y Aca Sci, 2001; 947:199-205.
[10] 姚树桐, 桑 慧, 杨娜娜等. 氧化低密度脂蛋白诱导巨噬细胞内质网应激及CD36的可能作用[J]. 生理学报, 2010; 62(5): 433-440.
[11] 卢卓强. ACE2-Ang-(1-7)-Mas轴:血管疾病治疗的新靶点[J]. 国际心血管病杂志, 2009; 36(1): 25-27.
[12] Thomas MC,?Pickering RJ,?Tsorotes D,?et al. Genetic Ace2 deficiency accentuates vascular inflammation and atherosclerosis in the ApoE knockout mouse[J]. Circ Res, 2010; 107(7): 888-897.
[13] Rabelo LA, Alenina N, Bader M, et al. ACE2-angiotensin-(1-7)-Mas axis and oxidative stress in cardiovascular disease. Hypertens Res, 2011; 34(2):154-160.
[14] Yang JM, Dong M, Meng X, et al. Angiotensin-(1-7) dose-dependently inhibits atherosclerotic lesion formation and enhances plaque stability by targeting vascular cells. Arterioscler Thromb Vasc Biol, 2013; 33(8):1978-1985.
[15] Gwathmey TM, Pendergrass KD, Reid SD, et al. Angiotensin-(1-7)-angiotensin-converting enzyme 2 attenuates reactive oxygen species formation to angiotensinⅡwithin the cell nucleus[J]. Hypertensio, 2010; 55(1):166-171.
[16] Liao X, Wang L, Yang C, et al. Cyclooxygenase mediates cardioprotection of angiotensin-(1-7) against ischemia/reperfusion-induced injury through the inhibition of oxidative stress[J]. Mol Med Rep, 2011; 4(6):1145-1150.
[17] Yang XH, Wang YH, Wang JJ, et al. Role of angiotensin-converting enzyme (ACE and ACE2) imbalance on tourniquet-induced remote kidney injury in a mouse hindlimb ischemia-reperfusion model[J]. Peptides. 2012; 36(1):60-70.
[18] 李亚芯,徐晨阳,张东慧等. 血管紧张素转移酶2(ACE2)在糖尿病致大鼠肝脏氧化应激损伤中的作用及机制分析[J]. 食品科学, 2013; 34(07):279-283.

Accesses

Citation

Detail

Sections
Recommended

/