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Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke.
Wijerathne, Harshani; Witek, Malgorzata A; Jackson, Joshua M; Brown, Virginia; Hupert, Mateusz L; Herrera, Kristina; Kramer, Cameron; Davidow, Abigail E; Li, Yan; Baird, Alison E; Murphy, Michael C; Soper, Steven A.
Affiliation
  • Wijerathne H; Department of Chemistry, The University of Kansas, Lawrence, KS, 66047, USA.
  • Witek MA; Center of BioModular Multiscale Systems for Precision Medicine, The University of Kansas, Lawrence, KS, 66047, USA.
  • Jackson JM; Department of Chemistry, The University of Kansas, Lawrence, KS, 66047, USA.
  • Brown V; Center of BioModular Multiscale Systems for Precision Medicine, The University of Kansas, Lawrence, KS, 66047, USA.
  • Hupert ML; The University of Kansas Medical Center, Cancer Center, Kansas City, KS, 66160, USA.
  • Herrera K; Department of Chemistry, The University of North Carolina, Chapel Hill, NC, 27599, USA.
  • Kramer C; Department of Chemistry, The University of Kansas, Lawrence, KS, 66047, USA.
  • Davidow AE; Center of BioModular Multiscale Systems for Precision Medicine, The University of Kansas, Lawrence, KS, 66047, USA.
  • Li Y; Center of BioModular Multiscale Systems for Precision Medicine, The University of Kansas, Lawrence, KS, 66047, USA.
  • Baird AE; Bioengineering Program, The University of Kansas, Lawrence, KS, 66047, USA.
  • Murphy MC; Biofluidica, Inc., San Diego, CA, 92121, USA.
  • Soper SA; Department of Chemistry, The University of North Carolina, Chapel Hill, NC, 27599, USA.
Commun Biol ; 3(1): 613, 2020 10 26.
Article in En | MEDLINE | ID: mdl-33106557
ABSTRACT
Currently there is no in vitro diagnostic test for acute ischemic stroke (AIS), yet rapid diagnosis is crucial for effective thrombolytic treatment. We previously demonstrated the utility of CD8(+) T-cells' mRNA expression for AIS detection; however extracellular vesicles (EVs) were not evaluated as a source of mRNA for AIS testing. We now report a microfluidic device for the rapid and efficient affinity-enrichment of CD8(+) EVs and subsequent EV's mRNA analysis using droplet digital PCR (ddPCR). The microfluidic device contains a dense array of micropillars modified with anti-CD8α monoclonal antibodies that enriched 158 ± 10 nm sized EVs at 4.3 ± 2.1 × 109 particles/100 µL of plasma. Analysis of mRNA from CD8(+) EVs and their parental T-cells revealed correlation in the expression for AIS-specific genes in both cell lines and healthy donors. In a blinded study, 80% test positivity for AIS patients and controls was revealed with a total analysis time of 3.7 h.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Messenger / Gene Expression Regulation / Lab-On-A-Chip Devices / Extracellular Vesicles / Ischemic Stroke Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Commun Biol Year: 2020 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Messenger / Gene Expression Regulation / Lab-On-A-Chip Devices / Extracellular Vesicles / Ischemic Stroke Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Commun Biol Year: 2020 Document type: Article Affiliation country: Estados Unidos
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