TY - JOUR
T1 - Tracing behavior of endothelial cells promotes vascular network formation
AU - Yasuda, Noriko
AU - Sekine, Hidekazu
AU - Bise, Ryoma
AU - Okano, Teruo
AU - Shimizu, Tatsuya
N1 - Funding Information:
This work was supported by a grant from the Japan Society for the Promotion of Science (JSPS) through the “Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program),” initiated by the Council for Science and Technology Policy (CSTP). Ryoma Bise is a staff of Dai Nippon Printing Co., outside of submitted work; we report grant from Dai Nippon Printing Co. We thank Atsushi Miyawaki and Asako Sakaue-Sawano (Laboratory for Cell Function and Dynamics, Brain Science Institute, RIKEN) for providing Fucci plasmid. We thank Atsushi Miyawaki, Asako Sakaue-Sawano and Allan Nisbet for his useful comments and editing of the manuscript.
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - The in vitro formation of network structures derived from endothelial cells in grafts before transplantation contributes to earlier engraftment. In a previous study, endothelial cells migrated to form a net-shaped structure in co-culture. However, the specific network formation behavior of endothelial cells during migration remains unclear. In this study, we demonstrated the tracing behavior and cell cycle of endothelial cells using Fucci-labeled (Fluorescent Ubiquitination-based Cell Cycle Indicator) endothelial cells. Here, we observed the co-culture of Fucci-labeled human umbilical vein endothelial cells (HUVECs) together with normal human dermal fibroblasts (NHDFs) using time-lapse imaging and analyzed by multicellular concurrent tracking. In the G0/G1 period, HUVECs migrate faster than in the S/G2/M period, because G0/G1 is the mobile phase and S/G2/M is the proliferation phase in the cell cycle. When HUVECs are co-cultured, they tend to move randomly until they find existing tracks that they then follow to form clusters. Extracellular matrix (ECM) staining showed that collagen IV, laminin and thrombospondin deposited in accordance with endothelial cell networks. Therefore the HUVECs may migrate on the secreted ECM and exhibit tracing behavior, where the HUVECs migrate toward each other. These results suggested that ECM and a cell phase contributed to form a network by accelerating cell migration.
AB - The in vitro formation of network structures derived from endothelial cells in grafts before transplantation contributes to earlier engraftment. In a previous study, endothelial cells migrated to form a net-shaped structure in co-culture. However, the specific network formation behavior of endothelial cells during migration remains unclear. In this study, we demonstrated the tracing behavior and cell cycle of endothelial cells using Fucci-labeled (Fluorescent Ubiquitination-based Cell Cycle Indicator) endothelial cells. Here, we observed the co-culture of Fucci-labeled human umbilical vein endothelial cells (HUVECs) together with normal human dermal fibroblasts (NHDFs) using time-lapse imaging and analyzed by multicellular concurrent tracking. In the G0/G1 period, HUVECs migrate faster than in the S/G2/M period, because G0/G1 is the mobile phase and S/G2/M is the proliferation phase in the cell cycle. When HUVECs are co-cultured, they tend to move randomly until they find existing tracks that they then follow to form clusters. Extracellular matrix (ECM) staining showed that collagen IV, laminin and thrombospondin deposited in accordance with endothelial cell networks. Therefore the HUVECs may migrate on the secreted ECM and exhibit tracing behavior, where the HUVECs migrate toward each other. These results suggested that ECM and a cell phase contributed to form a network by accelerating cell migration.
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U2 - 10.1016/j.mvr.2015.12.005
DO - 10.1016/j.mvr.2015.12.005
M3 - Article
C2 - 26687561
AN - SCOPUS:84962264995
SN - 0026-2862
VL - 105
SP - 125
EP - 131
JO - Microvascular Research
JF - Microvascular Research
ER -