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Sökning: L773:1473 0197 OR L773:1473 0189 > (2015-2019) > Formation of precis...

Formation of precisely composed cancer cell clusters using a cell assembly generator (CAGE) for studying paracrine signaling at single-cell resolution

Fatsis-Kavalopoulos, Nikos (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Gradientech AB, Uppsala, Sweden
O'Callaghan, Paul (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Xie, Beichen (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
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Hernández Vera, Rodrigo (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Idevall Hagren, Olof, 1980- (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Kreuger, Johan, 1972- (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
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 (creator_code:org_t)
2019
2019
Engelska.
Ingår i: Lab on a Chip. - : ROYAL SOC CHEMISTRY. - 1473-0197 .- 1473-0189. ; 19:6, s. 1071-1081
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The function and behaviour of any given cell in a healthy tissue, or in a tumor, is affected by interactions with its neighboring cells. It is therefore important to create methods that allow for reconstruction of tissue niches in vitro for studies of cell-cell signaling and associated cell behaviour. To this end we created the cell assembly generator (CAGE), a microfluidic device which enables the organization of different cell types into precise cell clusters in a flow chamber compatible with high-resolution microscopy. In proof-of-concept paracrine signalling experiments, 4-cell clusters consisting of one pancreatic -cell and three breast cancer cells were formed. It has previously been established that extracellular ATP induces calcium (Ca2+) release from the endoplasmic reticulum (ER) to the cytosol before it is cleared back into the ER via sarcoplasmic/ER Ca2+ ATPase (SERCA) pumps. Here, ATP release from the -cell was stimulated by depolarization, and dynamic changes in Ca2+ levels in the adjacent cancer cells measured using imaging of the calcium indicator Fluo-4. We established that changes in the concentration of cytosolic Ca2+ in the cancer cells were proportional to the distance from the ATP-releasing -cell. Additionally, we established that the relationship between distance and cytosolic calcium changes were dependent on Ca2+-release from the ER using 5-cell clusters composed of one -cell, two untreated cancer cells and two cancer cells pretreated with Thapsigargin (to deplete the ER of Ca2+). These experiments show that the CAGE can be used to create exact cell clusters, which affords precise control for reductionist studies of cell-cell signalling and permits the formation of heterogenous cell models of specific tissue niches.

Ämnesord

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

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