Low-Intensity Ultrasound Modulates Ca2+ Dynamics in Human Mesenchymal Stem Cells via Connexin 43 Hemichannel

被引:28
|
作者
Yoon, Chi Woo [1 ]
Jung, Hayong [1 ]
Goo, Kyosuk [1 ]
Moon, Sunho [1 ]
Koo, Kweon Mo [1 ]
Lee, Nan Sook [1 ]
Weitz, Andrew C. [1 ,2 ]
Shung, K. Kirk [1 ]
机构
[1] Univ Southern Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, Inst Biomed Therapeut, Los Angeles, CA USA
基金
美国国家卫生研究院;
关键词
Calcium signaling; Mechanotransduction; Purinergic signaling; ATP; MAGNETIC-FIELD STIMULATION; PULSED ULTRASOUND; OSTEOGENIC DIFFERENTIATION; MICROBEAM STIMULATION; MECHANICAL-STRESS; CALCIUM; FREQUENCY; RELEASE; MECHANOTRANSDUCTION; PATHWAY;
D O I
10.1007/s10439-017-1949-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In recent years, ultrasound has gained attention in new biological applications due to its ability to induce specific biological responses at the cellular level. Although the biophysical mechanisms underlying the interaction between ultrasound and cells are not fully understood, many agree on a pivotal role of Ca2+ signaling through mechanotransduction pathways. Because Ca2+ regulates a vast range of downstream cellular processes, a better understanding of how ultrasound influences Ca2+ signaling could lead to new applications for ultrasound. In this study, we investigated the mechanism of ultrasound-induced Ca2+ mobilization in human mesenchymal stem cells using 47 MHz focused ultrasound to stimulate single cells at low intensities ( 110 mW/cm(2)). We found that ultrasound exposure triggers opening of connexin 43 hemichannels on the plasma membrane, causing release of ATP into the extracellular space. That ATP then binds to G-protein-coupled P2Y1 purinergic receptors on the membrane, in turn activating phospholipase C, which evokes production of inositol trisphosphate and release of Ca2+ from intracellular stores.
引用
收藏
页码:48 / 59
页数:12
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