Microfluidic isolation and transcriptome analysis of serum microvesicles

被引:448
作者
Chen, Chihchen [1 ]
Skog, Johan [2 ,3 ]
Hsu, Chia-Hsien [1 ]
Lessard, Ryan T. [2 ,3 ]
Balaj, Leonora [2 ,3 ]
Wurdinger, Thomas [2 ,3 ,4 ]
Carter, Bob S. [5 ]
Breakefield, Xandra O. [2 ,3 ]
Toner, Mehmet [1 ]
Irimia, Daniel [1 ]
机构
[1] Harvard Univ, Sch Med, Shriners Hosp Children,Massachusets Gen Hosp, BioMEMS Resource Ctr,Ctr Engn Med & Surg Serv, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neurosci Program,Dept Neurol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neurosci Program,Dept Radiol, Boston, MA 02114 USA
[4] Vrije Univ Amsterdam, Med Ctr, Dept Neurosurg, Neurooncol Res Grp, NL-1007 MB Amsterdam, Netherlands
[5] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
关键词
TUMOR-DERIVED EXOSOMES; POLYMERASE CHAIN-REACTION; DENDRITIC CELLS; DIAGNOSTIC BIOMARKERS; MAJOR INHIBITOR; PLASMA-MEMBRANE; CANCER; BLOOD; IDENTIFICATION; AMPLIFICATION;
D O I
10.1039/b916199f
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microvesicles (exosomes) shed from both normal and cancerous cells may serve as means of intercellular communication. These microvesicles carry proteins, lipids and nucleic acids derived from the host cell. Their isolation and analysis from blood samples have the potential to provide information about state and progression of malignancy and should prove of great clinical importance as biomarkers for a variety of disease states. However, current protocols for isolation of microvesicles from blood require high-speed centrifugation and filtration, which are cumbersome and time consuming. In order to take full advantage of the potential of microvesicles as biomarkers for clinical applications, faster and simpler methods of isolation will be needed. In this paper, we present an easy and rapid microfluidic immunoaffinity method to isolate microvesicles from small volumes of both serum from blood samples and conditioned medium from cells in culture. RNA of high quality can be extracted from these microvesicles providing a source of information about the genetic status of tumors to serve as biomarkers for diagnosis and prognosis of cancer.
引用
收藏
页码:505 / 511
页数:7
相关论文
共 47 条
[41]   PLATELET MEMBRANE ACTIVATION MARKERS ARE PREDICTIVE FOR INCREASED RISK OF ACUTE ISCHEMIC EVENTS AFTER PTCA [J].
TSCHOEPE, D ;
SCHULTHEISS, HP ;
KOLAROV, P ;
SCHWIPPERT, B ;
DANNEHL, K ;
NIEUWENHUIS, HK ;
KEHREL, B ;
STRAUER, B ;
GRIES, FA .
CIRCULATION, 1993, 88 (01) :37-42
[42]   DESIGN AND CONSTRUCTION OF A LINEAR SHEAR-STRESS FLOW CHAMBER [J].
USAMI, S ;
CHEN, HH ;
ZHAO, YH ;
CHIEN, S ;
SKALAK, R .
ANNALS OF BIOMEDICAL ENGINEERING, 1993, 21 (01) :77-83
[43]   Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells [J].
Valadi, Hadi ;
Ekstrom, Karin ;
Bossios, Apostolos ;
Sjostrand, Margareta ;
Lee, James J. ;
Lotvall, Jan O. .
NATURE CELL BIOLOGY, 2007, 9 (06) :654-U72
[44]   Fabrication and characterization of ultrahigh-volume-fraction aligned carbon nanotube-polymer composites [J].
Wardle, Brian L. ;
Saito, Diego S. ;
Garcia, Enrique J. ;
Hart, A. John ;
de Villoria, Roberto Guzman ;
Verploegen, Eric A. .
ADVANCED MATERIALS, 2008, 20 (14) :2707-+
[45]   Inhibition and facilitation of nucleic acid amplification [J].
Wilson, IG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (10) :3741-3751
[46]   IDH1 and IDH2 Mutations in Gliomas [J].
Yan, Hai ;
Parsons, D. Williams ;
Jin, Genglin ;
McLendon, Roger ;
Rasheed, B. Ahmed ;
Yuan, Weishi ;
Kos, Ivan ;
Batinic-Haberle, Ines ;
Jones, Sian ;
Riggins, Gregory J. ;
Friedman, Henry ;
Friedman, Allan ;
Reardon, David ;
Herndon, James ;
Kinzler, Kenneth W. ;
Velculescu, Victor E. ;
Vogelstein, Bert ;
Bigner, Darell D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (08) :765-773
[47]   PLATELET PROCOAGULANT ACTIVITY AND MICROVESICLE FORMATION - ITS PUTATIVE ROLE IN HEMOSTASIS AND THROMBOSIS [J].
ZWAAL, RFA ;
COMFURIUS, P ;
BEVERS, EM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1180 (01) :1-8