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首页> 外文期刊>Aging cell. >Vascular smooth muscle cell‐specific progerin expression in a mouse model of Hutchinson–Gilford progeria syndrome promotes arterial stiffness: Therapeutic effect of dietary nitrite
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Vascular smooth muscle cell‐specific progerin expression in a mouse model of Hutchinson–Gilford progeria syndrome promotes arterial stiffness: Therapeutic effect of dietary nitrite

机译:Hutchinson-Gilford早衰综合征小鼠模型中血管平滑肌细胞特异的早老蛋白表达促进动脉僵硬:饮食中亚硝酸盐的治疗作用

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Vascular stiffness is a major cause of cardiovascular disease during normal aging and in Hutchinson–Gilford progeria syndrome (HGPS), a rare genetic disorder caused by ubiquitous progerin expression. This mutant form of lamin A causes premature aging associated with cardiovascular alterations that lead to death at an average age of 14.6?years. We investigated the mechanisms underlying vessel stiffness in LmnasupG609G/G609G/sup mice with ubiquitous progerin expression, and tested the effect of treatment with nitrites. We also bred LmnasupLCS/LCS/supTie2Cresup+/tg/sup and LmnasupLCS/LCS/supSM22αCresup+/tg/sup mice, which express progerin specifically in endothelial cells (ECs) and in vascular smooth muscle cells (VSMCs), respectively, to determine the specific contribution of each cell type to vascular pathology. We found vessel stiffness and inward remodeling in arteries of LmnasupG609G/G609G/sup and LmnasupLCS/LCS/supSM22αCresup+/tg/sup , but not in those from LmnasupLCS/LCS/supTie2Cresup+/tg/supmice . Structural alterations in aortas of progeroid mice were associated with decreased smooth muscle tissue content, increased collagen deposition, and decreased transverse waving of elastin layers in the media. Functional studies identified collagen (unlike elastin and the cytoskeleton) as an underlying cause of aortic stiffness in progeroid mice. Consistent with this, we found increased deposition of collagens III, IV, V, and XII in the media of progeroid aortas. Vessel stiffness and inward remodeling in progeroid mice were prevented by adding sodium nitrite in drinking water. In conclusion, LmnasupG609G/G609G/sup arteries exhibit stiffness and inward remodeling, mainly due to progerin‐induced damage to VSMCs, which causes increased deposition of medial collagen and a secondary alteration in elastin structure. Treatment with nitrites prevents vascular stiffness in progeria.
机译:血管僵硬是正常衰老和Hutchinson-Gilford早衰综合症(HGPS)中心血管疾病的主要原因,Hutchinson-Gilford早衰综合症是由普遍存在的早衰素表达引起的罕见遗传疾病。核纤层蛋白A的这种突变形式会导致与心血管疾病相关的过早衰老,导致平均年龄为14.6岁的死亡。我们研究了普遍存在早老蛋白表达的Lmna G609G / G609G 小鼠血管僵硬的潜在机制,并测试了亚硝酸盐治疗的效果。我们还繁殖了Lmna LCS / LCS Tie2Cre + / tg 和Lmna LCS / LCS SM22αCre + / tg 小鼠,它们分别在内皮细胞(EC)和血管平滑肌细胞(VSMC)中分别表达早春素,以确定每种细胞类型对血管病理学的特定作用。我们发现Lmna G609G / G609G 和Lmna LCS / LCS SM22αCre + / tg 的动脉血管僵硬和向内重塑,但在Lmna LCS / LCS Tie2Cre + / tg 小鼠。早老小鼠主动脉的结构改变与平滑肌组织含量减少,胶原蛋白沉积增加以及培养基中弹性蛋白层的横向波动减少有关。功能研究确定胶原蛋白(不同于弹性蛋白和细胞骨架)是早衰小鼠主动脉僵硬的根本原因。与此一致的是,我们发现在早发型主动脉的培养基中胶原蛋白III,IV,V和XII的沉积增加。通过在饮用水中添加亚硝酸钠,可以防止早衰小鼠的血管僵硬和向内重塑。总之,Lmna G609G / G609G 动脉表现出僵硬和向内重塑,这主要是由于早老素诱导的对VSMC的损伤,从而引起内侧胶原沉积增加和弹性蛋白结构的二次改变。亚硝酸盐治疗可防止早衰的血管僵硬。

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