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慢性间歇性加载会改变成骨样细胞中的机械敏感通道特性。

Chronic, intermittent loading alters mechanosensitive channel characteristics in osteoblast-like cells.

作者信息

Duncan R L, Hruska K A

机构信息

Renal Division, Jewish Hospital, Washington University Medical Center, St. Louis, Missouri 63110.

出版信息

Am J Physiol. 1994 Dec;267(6 Pt 2):F909-16. doi: 10.1152/ajprenal.1994.267.6.F909.

Abstract

The effects of chronic, intermittent strain on the mechanosensitive cation (SA-cat) channels in UMR-106.01 osteoblast-like osteosarcoma cells were studied using patch-clamp techniques. Chronically strained cells demonstrated significantly larger increases in whole cell conductance when subjected to additional mechanical strain than nonstrained controls (69.0 +/- 15.1 vs. 14.1 +/- 3.1%; P < 0.001). This increase could be blocked by the SA-cat channel inhibitor, gadolinium, and corresponded to a three- to fivefold increase in SA-cat channel activity. Chronic strain increased the number of open channels in response to stretch and induced spontaneous SA-cat channel activity in 33% of the patches of strained cells. Graded increases in negative patch pressure demonstrated that SA-cat channels in chronically strained cells were activated at significantly lower levels of mechanical perturbation than nonstrained controls. These data suggest that chronic, cyclic strain reduces the activation threshold of the SA-cat channel and further strengthen our hypothesis that this channel may act as a mechanotransducer for the activation of bone remodeling by physical strain.

摘要

采用膜片钳技术研究了慢性间歇性应变对UMR-106.01成骨样骨肉瘤细胞中机械敏感阳离子(SA-cat)通道的影响。与未受应变的对照组相比,慢性应变细胞在受到额外机械应变时,全细胞电导的增加显著更大(69.0±15.1%对14.1±3.1%;P<0.001)。这种增加可被SA-cat通道抑制剂钆阻断,且对应于SA-cat通道活性增加三到五倍。慢性应变增加了拉伸时开放通道的数量,并在33%的应变细胞膜片中诱导了自发的SA-cat通道活性。负向膜片钳压力的梯度增加表明,慢性应变细胞中的SA-cat通道在比未受应变的对照组显著更低的机械扰动水平下被激活。这些数据表明,慢性循环应变降低了SA-cat通道的激活阈值,并进一步强化了我们的假设,即该通道可能作为物理应变激活骨重塑的机械转导器。

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