期刊文献+

内皮源性微粒的多面性

Study on Endothelial Microparticles
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摘要 内皮源性微粒是具有复杂的囊泡性结构,来源于激活或凋亡的内皮源性细胞。它们在凝血、炎症、内皮功能和血管新生中具有显著的作用,干扰血管的动态平衡,促进血管相关性疾病形成。在血管性疾病患者中,内皮源性微粒水平增高,它们能作为反应内皮功能的生化标记物。内皮微粒被发现可以推进细胞生存、发挥抗炎效应、抗凝血过程、诱导内皮再生,因此内皮微粒是有害的观点受到挑战。这被称为内皮微粒在血管动态平衡中的矛盾作用。 Endothelial microparticles (EMP) are complex vesicular structures and derived from activated or apoptotic endothelial cells. They play a significant role in coagulation, inflammation, endothelial function and angiogenesis, disturb the vascular homeo- stasis and contribute to the progression of vascular diseases. Elevated levels of EMP are found in the patients with vascular diseases, so they can be a surrogate marker of endothelial function. Studies show that EMP can promote cell survival, exert anti - inflammatory effects, counteract coagulation processes and induce endothelial regeneration. All of them are reviewed in this paper.
出处 《国际老年医学杂志》 2011年第6期251-257,共7页 International Journal of Geriatrics
基金 上海市浦东新区卫生系统重点学科群建设(PWZxkq2010-05)资助项目
关键词 凋亡 动脉粥样硬化 内皮功能 内皮 栓塞 血栓 血管生化血 微粒 Apoptosis Atherosclerosis Endothelial function Endothelium Thrombin Thrombosis Vascular biology Microparticles
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参考文献63

  • 1Chironi GN, Boulanger CM, Simon A, el al. Endo- thelial microparticles in diseases [ J ]. Cell Tissue Res, 2009, 335: 143-151.
  • 2Leroyer AS, Ebrahimian TG, Cochain C, et al. Mi- croparticles from ischemie muscle promotes postnatal vasculogenesis [J]. Circulation, 2009, 119: 2808- 2817.
  • 3Jimenez JJ, Jy W, Mauro LM, et al. Endothelial cells release phenotypieally and quantitatively distinct microp- articles in activation and apoptosis [ J]. Thromb Res, 2003, 109: 175-180.
  • 4Thomas GM, Panicot -Dubois L, Lacroix R, et al. Cancer cell - derived microparticles bearing P - selectin glycoprotein ligand 1 accelerate thrombus formation in vivo [J]. J Exp Med, 2009, 206: 1913-1927.
  • 5Chahed S, Leroyer AS, Benzerroug M, et al. In-creased vitreous shedding of microparticles in prolifera- tive diabetic retinopathy stimulates endothelial prolifer- ation [J]. Diabetes, 2010, 59.- 694-701.
  • 6Leroyer AS, Isobe H, Leseche G, et al. Cellular ori- gins and thrombogenic activity of microparticles isolated from human atherosclerotic plaques [ J ]. J Am Coll Cardiol, 2007, 49:772 -777.
  • 7Peterson DB, Sander T, Kaul S, et al. Comparative proteomic analysis of PAI - 1 and TNF - alpha - derived endothelial microparticles [J]. Proteomics, 2008, 8: 2430 - 2446.
  • 8Deregibus MC, Cantaluppi V, Calogero R, et al. En- dothelial progenitor cell derived microvesieles activate an angiogenic program in endothelial cells by a horizontal transfer of mRNA [ Jl- Blood, 2007, 110:2440 - 2448.
  • 9Zampetaki A, Kieehl S, Drozdov I, et al. Plasma mi- eroRNA profiling reveals loss of endothelial miR - 126 and other microRNAs in type 2 diabetes [ J]. Circ Res, 2010, 107: 810-817.
  • 10Ullal AJ, Pisetsky DS, Reich CF 3rd. Use of SYTO 13, a fluorescent dye binding nucleic acids, for the de- tection of microparticles in in vitro systems [ J]. Cy- tometry A, 2010, 77: 294-301.

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