Mechanically induced intercellular calcium communication in confined endothelial structures

被引:21
|
作者
Junkin, Michael [1 ]
Lu, Yi [1 ]
Long, Juexuan [2 ]
Deymier, Pierre A. [2 ]
Hoying, James B. [3 ]
Wong, Pak Kin [1 ]
机构
[1] Univ Arizona, Dept Aerosp & Mech Engn, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Mat Sci & Engn, Tucson, AZ 85721 USA
[3] Cardiovasc Innovat Inst, Louisville, KY 40202 USA
关键词
Plasma lithography; Micropatterning; Calcium; Endothelial cell; Cell signaling; COLLOIDAL QUANTUM DOTS; CELLS; ATP; STIMULATION; SECRETION; RELEASE; WAVES; FLOW;
D O I
10.1016/j.biomaterials.2012.11.060
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Calcium signaling in the diverse vascular structures is regulated by a wide range of mechanical and biochemical factors to maintain essential physiological functions of the vasculature. To properly transmit information, the intercellular calcium communication mechanism must be robust against various conditions in the cellular microenvironment. Using plasma lithography geometric confinement, we investigate mechanically induced calcium wave propagation in networks of human umbilical vein endothelial cells organized. Endothelial cell networks with confined architectures were stimulated at the single cell level, including using capacitive force probes. Calcium wave propagation in the network was observed using fluorescence calcium imaging. We show that mechanically induced calcium signaling in the endothelial networks is dynamically regulated against a wide range of probing forces and repeated stimulations. The calcium wave is able to propagate consistently in various dimensions from monolayers to individual cell chains, and in different topologies from linear patterns to cell junctions. Our results reveal that calcium signaling provides a robust mechanism for cell cell communication in networks of endothelial cells despite the diversity of the microenvironmental inputs and complexity of vascular structures. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2049 / 2056
页数:8
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