4.3 Article

Sheathless acoustic based flow cell sorter for enrichment of rare cells

期刊

CYTOMETRY PART A
卷 101, 期 4, 页码 311-324

出版社

WILEY
DOI: 10.1002/cyto.a.24521

关键词

bulk acoustic wave; microfluidic fluorescence activated cell sorting; piezoelectric transducer; rare cell

资金

  1. National key research and development program of China [2016YFC1000701]
  2. Equipment development project of Chinese Academy of Sciences [ZDKYYQ20180003, ZDKYYQ20200004]
  3. Major innovation project of Shandong Province [2019JZZY011102]
  4. Science and Technology project of Suzhou [SS2019067]

向作者/读者索取更多资源

Cell enrichment is a powerful tool in various cell research applications, especially for low abundance cell types. A microfluidic fluorescence activated cell sorting device was developed to detect and sort cells with high efficiency. The device was able to remove over 98% of white blood cells and recover labeled lymphocytes with 80% efficiency, as well as successfully isolating fetal nucleated red blood cells from clinical samples for genetic analysis, showing potential for biomedical applications involving fetal cells, circulating tumor cells, and stem cells.
Cell enrichment is a powerful tool in many kinds of cell research, especially in applications with low abundance cell types. In this work, we developed a microfluidic fluorescence activated cell sorting device that was able to perform on-demand, low loss cell detection, and sorting. The chip utilizes three-dimensional acoustic standing waves to position all cells in the same fluid velocity regime without sheath. When the cells pass through a laser interrogation region, the scattering and fluorescent signals are detected, translated and transported to software. The target cells are then identified by gating on the plots. Short bursts of standing acoustic waves are triggered by order from PC to sort target cells within predefined gating region. For very low abundance and rare labeled lymphocytes mixed with high concentration unlabeled white blood cells (WBCs), (1-100 labeled lymphocytes are diluted in 10(6) WBCs in 1 ml volume fluid), the device is able to remove more than 98% WBCs and recover labeled lymphocytes with efficiency of 80%. We further demonstrated that this device worked with real clinical samples by successfully isolating fetal nucleated red blood cells (FNRBCs) in the blood samples from pregnant women with male fetus. The obtained cells were sequenced and the expressions of (sex determining region Y) SRY genes were tested to determine fetal cell proportion. In genetic analysis, the proportion of fetal cells in the final picked sample is up to 40.64%. With this ability, the device proposed could be valuable for biomedical applications involving fetal cells, circulating tumor cells, and stem cells.

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