Yao Jessica, Qin Zhenyu
Division of Vascular Surgery, Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
Division of Vascular Surgery, Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
J Trace Elem Med Biol. 2015;31:11-7. doi: 10.1016/j.jtemb.2015.02.003. Epub 2015 Feb 21.
Bone marrow of blotchy mouse (blotchy marrow) reflects the function of transmembrane domain and relevant intramembrane sites of ATP7A in myeloid cells. By chronic infusion of angiotensin II, we previously found that blotchy marrow plays a minor role in regulating plasma copper. Moreover, the recipients of blotchy marrow presented a moderate reduction of plasma lipids and inflammatory mediator production. Little is known about whether these changes are a specific response to angiotensin II or reveal a more general role of ATP7A.
We investigated if blotchy marrow reduces plasma lipids and inflammatory mediators induced by high-fat diets. To test this hypothesis, blotchy and control marrows were reconstituted to the recipient mice (irradiated male LDLR-/- mice), followed by high-fat-diet feeding for 4 months. At the end points, plasma metals (copper, zinc and iron), lipid profiling (cholesterol, triglyceride, phospholipids and lipoprotein) and six inflammatory mediators (lymphotacin, MCP3, MCP5, TIMP1, VEGF-A and IP-10) were measured. Parallel experiments were performed using male LDLR-/- mice fed either high-fat diets or chow diets for 4 months.
In addition to hyperlipidemia and low-grade inflammation, high-fat diets selectively increased plasma copper concentration compared to chow diets in LDLR-/- mice. After high-fat-diet feeding, the recipients with blotchy marrow showed a decrease in plasma copper (p < 0.01) and an increase in plasma iron (p < 0.05). The recipients with blotchy marrow also presented decreases in cholesterol (p < 0.01) and phospholipids (p < 0.05) in plasma. Surprisingly, plasma levels of MCP3 (p < 0.05), MCP5 (p < 0.05), TIMP1 (p < 0.01), VEGF-A (p < 0.01) and IP-10 (p < 0.01) were significantly increased in the recipients with blotchy marrow compared to controls; the increased levels of MCP3, MCP5 and TIMP1 were more than 50%.
Our studies showed that blotchy marrow counteracts the increased copper levels induced by high-fat diets, indicating that circulating myeloid cells can regulate blood copper levels via ATP7A. Moreover, transplantation of blotchy marrow followed by high-fat diets leads to a decrease in lipid profile and an increase in inflammatory mediator production. Overall, blotchy marrow mediates divergent responses to angiotensin II and high-fat diets in vivo.
斑驳小鼠的骨髓(斑驳骨髓)反映了髓系细胞中ATP7A跨膜结构域及相关膜内位点的功能。通过慢性输注血管紧张素II,我们先前发现斑驳骨髓在调节血浆铜方面作用较小。此外,接受斑驳骨髓移植的小鼠血浆脂质和炎症介质生成有适度减少。对于这些变化是对血管紧张素II的特异性反应还是揭示了ATP7A更普遍的作用,人们知之甚少。
我们研究了斑驳骨髓是否能降低高脂饮食诱导的血浆脂质和炎症介质。为验证这一假设,将斑驳骨髓和对照骨髓移植到受体小鼠(经辐照的雄性LDLR-/-小鼠)体内,随后给予高脂饮食喂养4个月。在实验终点,检测血浆金属(铜、锌和铁)、脂质谱(胆固醇甘油三酯、磷脂和脂蛋白)以及六种炎症介质(淋巴细胞趋化因子、MCP3、MCP5、TIMP1、VEGF-A和IP-10)。使用喂食高脂饮食或普通饮食4个月的雄性LDLR-/-小鼠进行平行实验。
与普通饮食相比,高脂饮食除了导致LDLR-/-小鼠出现高脂血症和低度炎症外,还选择性地增加了血浆铜浓度。高脂饮食喂养后,接受斑驳骨髓移植的小鼠血浆铜水平降低(p<0.01),血浆铁水平升高(p<0.05)。接受斑驳骨髓移植的小鼠血浆中的胆固醇(p<0.01)和磷脂(p<0.05)水平也有所降低。令人惊讶的是,与对照组相比,接受斑驳骨髓移植的小鼠血浆中MCP3(p<0.05)、MCP5(p<0.05)、TIMP1(p<0.01)、VEGF-A(p<0.01)和IP-10(p<0.01)的水平显著升高;MCP3、MCP5和TIMP1升高的水平超过50%。
我们的研究表明,斑驳骨髓可抵消高脂饮食诱导的铜水平升高表明循环髓系细胞可通过ATP7A调节血铜水平。此外,移植斑驳骨髓后再给予高脂饮食会导致脂质谱降低和炎症介质生成增加。总体而言,斑驳骨髓在体内介导了对血管紧张素II和高脂饮食的不同反应。