細胞運動を追跡する新しい全電気式イメージング技術(All-electrical imaging offers innovative alternative for tracking cell movement)

2026-10-07 ブラウン大学

米ブラウン大学の研究者らは、光学レンズや蛍光標識を使わず、電気容量(静電容量)の変化から細胞の移動を追跡するマイクロチップ型イメージング技術を開発した。約0.5インチ角のチップ上に100万個の微小電極を配置し、細胞が表面に接触して移動すると生じる局所的な静電容量の変化を検出する。これにより、蛍光色素による細胞へのダメージや光学顕微鏡特有の画像処理負荷を抑えながら、細胞の移動を自動追跡できる。実験ではヒト乳がん細胞の移動・分裂や、多細胞スフェロイドの「リーダー細胞」の移動を可視化し、さらに数十万個の細胞からなる組織の形状変化も検出した。大面積・小型・低コスト化が可能で、がん転移、創傷治癒、免疫応答などの研究への応用が期待される。

細胞運動を追跡する新しい全電気式イメージング技術(All-electrical imaging offers innovative alternative for tracking cell movement)

<関連情報>

メガピクセルCMOS容量センサーを用いた、ラベルフリーの全電気式による個々の細胞および集団細胞の移動追跡

Label-Free All-Electrical Tracking of Individual and Collective Cell Migration on a Megapixel CMOS Capacitance Sensor

Hyuntae Jeong;Pushkaraj Joshi;Yinshi Hu;Jiwon Kim;Anh H Vu;Jacob K Rosenstein;Ian Y Wong

Lab on a Chip  Published:30 September 2026

DOI:https://doi.org/10.1039/D6LC00530F

Label-free tracking of adherent cell migration could enable important insights into biological processes such as tissue repair, inflammatory response, or cancer progression. Nevertheless, visualizing unlabeled animal cells using optical microscopy remains challenging due to low contrast as well as frequent changes in cell shape and number. A promising alternative uses electrical capacitance measurements, which are sensitive to cell adhesion to electrode surfaces. However, prior examples often utilized electrodes with areas larger than single cells, resulting in averaged readouts over multiple cells. Here, we demonstrate label-free, live-cell tracking using a capacitance sensor array with more than 1 million pixels on a 10 micron pitch across an area larger than 1 square centimeter. We show that single cell morphology can be clearly segmented, and then used to reconstruct migration and proliferation dynamics using optical flow. We further track the spreading of multicellular spheroids, revealing fast-moving peripheral regions led by a collective leader cell “front.” Finally, we demonstrate label-free imaging of millimeter-scale honeycomb-shaped tissues without the multi-image stitching often required for conventional microscopy. We utilize mutual capacitance measurements with electrically-programmable electrode spacing to reconstruct topographical features of these engineered tissues. Overall, CMOS capacitance imaging arrays enables label-free imaging spanning from single cells to large tissues, in a portable and scalable format for settings where optical microscopy may be difficult to access.

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