AI Article Synopsis

  • Human induced pluripotent stem cells (hiPSCs) can differentiate into three types of cells (ectoderm, mesoderm, endoderm) on specialized chips, allowing for consistent and precise analysis of their pluripotency.
  • A new U-Net structure called MP-UNet is proposed for accurately segmenting and analyzing the early spatial patterns of hiPSCs using fluorescence images, with features that adapt to different image sizes.
  • The MP-UNet employs specific loss functions to enhance accuracy in detecting cell regions, proving effective across various sizes of images, making it a valuable tool for studying hiPSC behavior on micropatterned chips.

Article Abstract

Human induced pluripotent stem cells (hiPSCs) can differentiate into three germ layer cells, i.e. ectoderm, mesoderm and endoderm, on micropatterned chips in highly synchronous and reproducible manners. The cells are confined within the chip, expanding two-dimensionally as almost in the form of monolayer, thus to be ideal for serving quantitative analysis of their pluripotency. We present a new U-Net (MP-UNet) structure for cell segmentation of early spatial patterning of hiPSCs on micropattern chips using Hoechst fluorescence images. In this structure, the encoding/decoding layers can be dynamically adjusted to extract sufficient image features and be flexible to image sizes. Dice and weight loss functions are designed to identify slight difference in low signal-to-noise ratio, high boundary-to-area ratio and compacted cell images. Several sizes of Hoechst images were tested to show MP-UNet can achieve high accuracy in cell regions and number counting for various sizes of micropattern chips, thus to be excellent quantitative tool for early spatial patterning of hiPSCs.

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Source
http://dx.doi.org/10.1109/EMBC46164.2021.9630956DOI Listing

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