TY - GEN
T1 - A novel double-layer parallel-plate flow chamber
AU - Won, Hee Lee
AU - Kang, Sungkwon
AU - Hirani, Anjali A.
AU - Yong, Woo Lee
PY - 2007
Y1 - 2007
N2 - In the present study, we designed and developed a novel double-layer parallel-plate flow chamber (PPFC) to study the dynamic response of vascular endothelial cells to controlled levels of shear stress. In addition, the effects of fluid shear stress on the structure and function of endothelial cells were examined to validate whether a novel PPFC can be employed for studies in the areas of biomedical research. Human microvascular endothelial cells (HMEC-1) were either maintained in static condition or exposed to laminar flow for 24 h. The morphological changes and attenuated expression of pro-inflammatory mediators, such as ICAM-1, VCAM-1, and E-selectin were observed in endothelial cells exposed to the flow. HMEC-1 cells were also either maintained in continuous laminar flow (Normal flow) or subjected to 1 h of flow cessation followed by reperfusion (12 h) of flow (Ischemia/Reperfusion). The real-time RT-PCR analysis showed that Ischemia/Reperfusion significantly up-regulated expression of pro-inflammatory mediators in HMEC-1 compared to Normal flow, which is consistent with previous in vivo studies. These data indicate that our newly designed PPFC can provide a better in vitro system for versatile applications of biomedical research.
AB - In the present study, we designed and developed a novel double-layer parallel-plate flow chamber (PPFC) to study the dynamic response of vascular endothelial cells to controlled levels of shear stress. In addition, the effects of fluid shear stress on the structure and function of endothelial cells were examined to validate whether a novel PPFC can be employed for studies in the areas of biomedical research. Human microvascular endothelial cells (HMEC-1) were either maintained in static condition or exposed to laminar flow for 24 h. The morphological changes and attenuated expression of pro-inflammatory mediators, such as ICAM-1, VCAM-1, and E-selectin were observed in endothelial cells exposed to the flow. HMEC-1 cells were also either maintained in continuous laminar flow (Normal flow) or subjected to 1 h of flow cessation followed by reperfusion (12 h) of flow (Ischemia/Reperfusion). The real-time RT-PCR analysis showed that Ischemia/Reperfusion significantly up-regulated expression of pro-inflammatory mediators in HMEC-1 compared to Normal flow, which is consistent with previous in vivo studies. These data indicate that our newly designed PPFC can provide a better in vitro system for versatile applications of biomedical research.
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U2 - 10.1109/NEBC.2007.4413400
DO - 10.1109/NEBC.2007.4413400
M3 - Conference contribution
AN - SCOPUS:48749130138
SN - 1424410339
SN - 9781424410330
T3 - Proceedings of the IEEE Annual Northeast Bioengineering Conference, NEBEC
SP - 309
EP - 310
BT - 33rd Annual Northeast Bioengineering Conference - Engineering Innovations in Life Sciences and Healthcare, NEBC
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 33rd Annual Northeast Bioengineering Conference, NEBC
Y2 - 10 March 2007 through 11 March 2007
ER -