期刊文献+

血小板微粒相关研究进展 被引量:4

Relevant Research Progress of Platelet Micropaticles
下载PDF
导出
摘要 血液中的细胞微粒可来自多种细胞,但血小板微粒(platelet microparticle,PMP)占多数。PMP是一群特殊的微粒群,既不同于多泡体产生的外体,也不同于巨核细胞源性的微粒。PMP具有完整的血小板膜蛋白和膜脂质等膜结构。不同类型的激活剂诱导形成的PMP具有多样性。PMP发挥重要的生理功能,可以协同血小板作用。此外,研究发现PMP还可介导生物活性分子在细胞间的传递,例如表面受体、胞质蛋白或RNA等,促进细胞-细胞间相互作用。近年鉴于在多种疾病患者体内均发现PMP异常,例如特发性血小板减少性紫癜、前列腺癌和风湿性关节炎等。从PMP的形成和多样性、来源、生物学功能及其相关临床疾病等方面进行综述,以期更全面、确切地揭示PMP的特性、不同病理及其相关分子机制,更好地指导进一步临床研究,为新的治疗方法提供理论基础。 Platelet microparticles(PMP) are the most abundant microparticles in the bloodstream which constituting microparticles come from a variety of cells. PMP are a heterogeneous population of vesicles. They are not only different from the exosomes which generated from the intracellular multivesicular bodies,but also different from the microparticles derived from megakaryocytes. PMP have intact membrane glycoprotein and lipid composition that is same with platelet. The diversity of PMP which induced by different activators play an important role in physiological function. PMP can work in coordination with platelet.Furthermore,it is now accepted that PMP mediate intercellular transfer of bioactive molecules for a better promotion of cell-cell communication,for instance,delivering membrane receptors,cytoplasmic proteins and even RNA to recipient cells. Recent researches have shown that the unusual level of PMP had found in patients with certain diseases,such as immune thrombocytopenic purpura,prostate cancer,rheumatoid arthritis,etc. This article reviewed the formation and diversity,generation,biological function of PMP and its related clinical diseases so as to promulgate the properties of PMP and multiple pathology progresses and relevant molecular mechanisms more inclusively and more correctly,to better guide the further clinical research,providing theoretical basis for new treatment methods.
作者 姜璐 汪希鹏
出处 《国际妇产科学杂志》 CAS 2015年第3期306-310,共5页 Journal of International Obstetrics and Gynecology
关键词 血小板微粒 血栓形成 炎症 肿瘤转移 Platelet microparticles Thrombosis Inflammation Neoplasm metastasis
  • 相关文献

参考文献28

  • 1Thry C ,Zitvogel L, Amigorena S. Exosomes: composition, biogenesis and function[J]. Nat Rev Immunol, 2002,2(8 ) : 569-579.
  • 2Raiborg C, Stenmark H. The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins [J]. Nature,2009,458 (7237): 445 -452.
  • 3Hurley JH,Hanson PI. Membrane budding and scission by the ESCRT machinery:it's all in the neck [J]. Nat Rev Mol Cell Biol, 2010,11 (8) : 556-566.
  • 4Ostrowski M,Carmo NB,Krumeich S,et al. Rab27a and Rab27b control different steps of the exosome secretion pathway [J]. Nat Cell Biol, 2010,12( 1 ) : 19-30.
  • 5Peinado H, Alekovi M,Lavotshkin S,et al. Melanoma exosomes educate bone marrow progenitor cells toward a pro-metastatic phenotype through MET[J]. Nat Med,2012,18(6):883-891.
  • 6Savina A,Fader CM,Damiani MT,et al. Rabll promotes docking and fusion of multivesicular bodies in a calcium-dependent manner [J]. Traffic, 2005,6 (2) : 131-143.
  • 7Monteealvo A,Shufesky WJ,Stolz DB,et al. Exosomes as a short- range mechanism to spread alloantigen between dendritic cells during T cell alloreeognition [J]. J Immunol, 2008,180 (5) : 3081 - 3090.
  • 8Larson MC,Hillery CA,Hogg N. Circulating membrane-derived microvesicles in redox biology [J]. Free Radic Biol Med,2014,73C: 214-228.
  • 9Fader CM,SOnchez DG,Mestre MB,et al. TI-VAMP/VAMP7 and VAMP3/cellubrevin: two v-SNARE proteins involved in specific steps of the autophagy/multivesicular body pathways [J]. Biochim Biophys Aeta, 2009,1793(12) : 1901-1916.
  • 10Shai E, Rosa I, Parguifia AF, et al. Comparative analysis of platelet- derived naicroparticles reveals differences in their amount and proteome depending on the platelet stimulus [J]. J Proteomics, 2012 Dec 5. [Epub 2012 Mar 5].

同被引文献37

引证文献4

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部