Recapitulating the Drifting and Fusion of Two-Generation Spheroids on Concave Agarose Microwells

Abstract

Cells with various structures and proteins naturally come together to cooperate in vivo. This study used cell spheroids cultured in agarose micro-wells as a 3D model to study the movement of cells or spheroids toward other spheroids. The formation dynamics of tumor spheroids and the interactions of two batches of cells in the agarose micro-wells were studied. The results showed that a concave bottom micro-well (diameter: 2 mm, depth: 2 mm) prepared from 3% agarose could be used to study the interaction of two batches of cells. The initial tumor cell numbers from 5 × 103 cells/well to 6 × 104 cells/well all could form 3D spheroids after 3 days of incubation. Adding the second batch of DU 145 cells to the existing DU 145 spheroid resulted in the formation of satellite cell spheroids around the existing parental tumor spheroid. Complete fusion of two generation cell spheroids was observed when the parental spheroids were formed from 1 × 104 and 2 × 104 cells, and the second batch of cells was 5 × 103 per well. A higher amount of the second batch of cells (1 × 104 cell/well) led to the formation of independent satellite spheroids after 48 h of co-culture, suggesting the behavior of the second batch of cells towards existing parental spheroids depended on various factors, such as the volume of the parental spheroids and the number of the second batch cells. The interactions between the tumor spheroids and Human Umbilical Vein Endothelial Cells (HUVECs) were modeled on concave agarose micro-wells. The HUVECs (3 × 103 cell/well) were observed to gather around the parental tumor spheroids formed from 1 × 104, 2 × 104, and 3 × 104 cells per well rather than aggregate on their own to form HUVEC spheroids. This study highlights the importance of analyzing the biological properties of cells before designing experimental procedures for the sequential fusion of cell spheroids. The study further emphasizes the significant roles that cell density and the volume of the spheroids play in determining the location and movement of cells.

High throughput generating stable spheroids with tip‐refill wafer

“…Then, DU 145 (6 × 10 5 cells mL −1 ) and DiO-labeled HUVEC cells (2 × 10 5 cells mL −1 ) were mixed in a ratio of 10:3. [17] 60-μL the mixed cell suspension was pipetted to the TrW. The formation of the multicellular spheroids was observed and captured under the fluorescence microscope at different time points (0, 12, 24, and 48 h).…”

The influence of spheroid maturity on fusion dynamics and micro-tissue assembly in 3D tumor models

“…Spheroids formation and fusion process was illustrated in schematic 1A. The design and fabrication of concave agarose micro-well array have been described in previous study [31]. In brief, a mold with a Ushaped protrusion was created using 3D printing technology.…”