TY - CHAP
T1 - Micro-vessel network formation of endothelial cells with in vitro three dimensional model
AU - Tanishita, K.
AU - Ueda, A.
AU - Koga, M.
AU - Sudo, R.
AU - Kudo, S.
AU - Ikeda, M.
PY - 2006/1/1
Y1 - 2006/1/1
N2 - Bovine pulmonary microvascular endothelial cells were seeded onto collagen gels with basic fibroblast growth factor (bFGF) to make a micro-vessel formation model. We observed this model in detail using phase contrast microscopy, confocal laser scanning microscopy and electron microscopy. The results show that cells invaded the collagen gel and reconstructed the tubular structures, containing a clearly defined lumen consisting of multiple cells. The model was placed in a parallel-plate flow chamber. A laminar shear stress of 0.3 Pa was applied to the surfaces of the cells for 48 hours. Promotion of micro-vessel network formation was detectable after approximately 10 hours in the flow chamber. After 48 hours, the length of networks exposed to shear stress was 6.17 (± 0.59) times longer than at the initial state, whereas the length of networks not exposed to shear stress was only 3.30 (± 0.41) times longer. The number of bifurcations and endpoints increased for networks exposed to shear stress, whereas the number of bifurcations alone increased for networks not exposed to shear stress. These results demonstrate that shear stress applied to the surfaces of endothelial cells on collagen gel promotes the growth of micro-vessel network formation in the gel and expands the network due to repeated bifurcation and elongation.
AB - Bovine pulmonary microvascular endothelial cells were seeded onto collagen gels with basic fibroblast growth factor (bFGF) to make a micro-vessel formation model. We observed this model in detail using phase contrast microscopy, confocal laser scanning microscopy and electron microscopy. The results show that cells invaded the collagen gel and reconstructed the tubular structures, containing a clearly defined lumen consisting of multiple cells. The model was placed in a parallel-plate flow chamber. A laminar shear stress of 0.3 Pa was applied to the surfaces of the cells for 48 hours. Promotion of micro-vessel network formation was detectable after approximately 10 hours in the flow chamber. After 48 hours, the length of networks exposed to shear stress was 6.17 (± 0.59) times longer than at the initial state, whereas the length of networks not exposed to shear stress was only 3.30 (± 0.41) times longer. The number of bifurcations and endpoints increased for networks exposed to shear stress, whereas the number of bifurcations alone increased for networks not exposed to shear stress. These results demonstrate that shear stress applied to the surfaces of endothelial cells on collagen gel promotes the growth of micro-vessel network formation in the gel and expands the network due to repeated bifurcation and elongation.
UR - http://www.scopus.com/inward/record.url?scp=84969247003&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84969247003&partnerID=8YFLogxK
U2 - 10.1142/9789812773838_0003
DO - 10.1142/9789812773838_0003
M3 - Chapter
AN - SCOPUS:84969247003
SN - 9789812773838
SN - 9812567461
SN - 9789812567468
VL - 2
SP - 26
EP - 36
BT - Biomechanics at Micro- and Nanoscale Levels
PB - World Scientific Publishing Co.
ER -