Lei Xin-jun, Ma Ai-qun, Xi Yu-tao, Zhang Wei, Yao Yan, Du Yuan
Department of Cardiology, Key Laboratory of Environment and Genes Related to Diseases, Ministry of Education, Cardiovascular Ion Channelopathy Laboratory, the First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710061, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2006 May;22(3):310-3.
To investigate the expression of high-conductance Ca2+-activated potassium channel (MaxiK channel) mRNA and protein during human monocyte-derived macrophage differentiation into foam cells and to study its function in foam cell formation.
Human peripheral blood monocytes were isolated from healthy male volunteers by density gradient centrifugation and then by adherent method. The obtained monocytes were cultured for 5 days to differentiate into macrophages. Based on establishment of human macrophage-derived foam cells model, the expression of MaxiK channel alpha-subunit was investigated by immunocytochemical staining, RT-PCR and Western blot. Furthermore, the effect of Paxilline, a MaxiK channel-specific inhibitor, on cholesterol metabolism in macrophages incepting oxidized low density lipoprotein (OxLDL) was studied.
After the macrophages were co-incubated with 30 mg/L OxLDL at 37 degrees C for 60 hours, the cellular volume obviously enlarged and many red lipid granules were deposited in cytoplasm. The total amount of cholesterol (TC), free cholesterol (FC) and cholesterol ester (CE) in cells markedly increased and the ratio of CE/TC rose from (14.437+/-6.781)% to (57.946+/-3.507)% (n=7, P<0.05). However, the expression of MaxiK channel alpha-subunit had no significant change (P<0.05). Paxilline (5 micromol/L and 10 micromol/L) markedly reduced the content of TC, FC and CE in macrophages and the ratio of CE/TC decreased to (41.217+/-5.584)% (5 micromol/L Paxilline) and (18.017+/-11.559)% (10 micromol/L Paxilline), respectively (n=7, P<0.05). Meanwhile, the red lipid granules deposited in the cytoplasm of macrophages also decreased.
Blocking MaxiK channel can inhibit human monocyte-derived macrophage to be differentiated into foam cells.
研究人单核细胞衍生的巨噬细胞分化为泡沫细胞过程中高电导钙激活钾通道(大电导钙激活钾通道,MaxiK通道)mRNA和蛋白的表达情况,并探讨其在泡沫细胞形成中的作用。
通过密度梯度离心法,随后采用贴壁法从健康男性志愿者外周血中分离单核细胞。将获得的单核细胞培养5天使其分化为巨噬细胞。基于建立人巨噬细胞源性泡沫细胞模型,采用免疫细胞化学染色、逆转录-聚合酶链反应(RT-PCR)及蛋白质免疫印迹法(Western blot)研究MaxiK通道α亚基的表达。此外,研究MaxiK通道特异性抑制剂派迷西林(Paxilline)对摄取氧化型低密度脂蛋白(OxLDL)的巨噬细胞胆固醇代谢的影响。
巨噬细胞与30 mg/L OxLDL在37℃共孵育60小时后,细胞体积明显增大,胞质内可见大量红色脂滴沉积。细胞内总胆固醇(TC)、游离胆固醇(FC)及胆固醇酯(CE)含量显著增加,CE/TC比值从(14.437±6.781)%升至(57.946±3.507)%(n = 7,P < 0.05)。然而,MaxiK通道α亚基的表达无明显变化(P < 0.05)。派迷西林(5 μmol/L和10 μmol/L)显著降低巨噬细胞内TC、FC及CE含量,CE/TC比值分别降至(41.217±5.584)%(5 μmol/L派迷西林)和(18.017±11.559)%(10 μmol/L派迷西林)(n = 7,P < 0.05)。同时,巨噬细胞胞质内沉积的红色脂滴也减少。
阻断MaxiK通道可抑制人单核细胞衍生的巨噬细胞分化为泡沫细胞。