コンテンツへスキップ
Merck
  • Probing coordinated co-culture cancer related motility through differential micro-compartmentalized elastic substrates.

Probing coordinated co-culture cancer related motility through differential micro-compartmentalized elastic substrates.

Scientific reports (2020-10-30)
Szu-Yuan Chou, Chang-You Lin, Theresa Cassino, Li Wan, Philip R LeDuc
要旨

Cell development and behavior are driven by internal genetic programming, but the external microenvironment is increasingly recognized as a significant factor in cell differentiation, migration, and in the case of cancer, metastatic progression. Yet it remains unclear how the microenvironment influences cell processes, especially when examining cell motility. One factor that affects cell motility is cell mechanics, which is known to be related to substrate stiffness. Examining how cells interact with each other in response to mechanically differential substrates would allow an increased understanding of their coordinated cell motility. In order to probe the effect of substrate stiffness on tumor related cells in greater detail, we created hard-soft-hard (HSH) polydimethylsiloxane (PDMS) substrates with alternating regions of different stiffness (200 and 800 kPa). We then cultured WI-38 fibroblasts and A549 epithelial cells to probe their motile response to the substrates. We found that when the 2 cell types were exposed simultaneously to the same substrate, fibroblasts moved at an increased speed over epithelial cells. Furthermore, the HSH substrate allowed us to physically guide and separate the different cell types based on their relative motile speed. We believe that this method and results will be important in a diversity of areas including mechanical microenvironment, cell motility, and cancer biology.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
4-(ジメチルアミノ)ピリジン、ポリマー担持型, extent of labeling: ~3.0 mmol/g "DMAP" loading, matrix crosslinked with 2% DVB
Sigma-Aldrich
抗サイトケラチンAE1/AE3抗体 クローンAE1/AE3、酸性および塩基性サイトケラチンを認識, clone AE1/AE3, Chemicon®, from mouse