2016
DOI: 10.3892/br.2016.595
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Fluid shear stress enhances the cell volume decrease of osteoblast cells by increasing the expression of the ClC-3 chloride channel

Abstract: Abstract. ClC-3 is a volume-sensitive chloride channel that is responsible for cell volume adjustment and regulatory cell volume decrease (RVD). In order to evaluate the effects of fluid shear stress (FSS) stimulation on the osteoblast ClC-3 chloride channel, MC3T3-E1 cells were stimulated by FSS in the experimental group. Fluorescence quantitative polymerase chain reaction was used to detect changes in ClC-3 mRNA expression, the chloride ion fluorescent probe N-(ethoxycarbonylmethyl)-6-methoxyquinolinium brom… Show more

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Cited by 7 publications
(4 citation statements)
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“…Tissues exposed to the medium flow also appeared slightly thinner. As previously demonstrated with osteoblasts 49 or C11-MDCK cells, 50 the shear stress caused by the medium flow could have decreased cell volume, thereby changing tissue thickness. While the shear stress caused by the medium flow might explain this observation, 51 there is currently no evidence that such mechanical stress across a porous membrane (10 μm thickness) could have affected the tissues.…”
Section: Stability Of the Nhbe Ali Or Heparg™ Spheroid Monocultures-imentioning
confidence: 70%
“…Tissues exposed to the medium flow also appeared slightly thinner. As previously demonstrated with osteoblasts 49 or C11-MDCK cells, 50 the shear stress caused by the medium flow could have decreased cell volume, thereby changing tissue thickness. While the shear stress caused by the medium flow might explain this observation, 51 there is currently no evidence that such mechanical stress across a porous membrane (10 μm thickness) could have affected the tissues.…”
Section: Stability Of the Nhbe Ali Or Heparg™ Spheroid Monocultures-imentioning
confidence: 70%
“…[ 27 , 31 ] The involvement of the CaCCs in the process of cell morphological change is closely related to cell migration and invasion. [ 32 , 33 , 34 ] Therefore, we performed live cell time‐lapse imaging to detect the tracking plots from BEST1 overexpression (O.E. ), BEST1 knockout (K.O.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, ClC-3 mediated RVD can induce VEC apoptosis, resulting in increased arterial intimal permeability and endothelial injury. 58 Previous reports have revealed that upregulation of ClC-3 induces VEC atrophy, as well as delocalization of LDL into the subintima. 15 These findings indicate that the ClC-3 mediated RVD function may be one mechanism responsible for the progressive accumulation of LDL in the subintima.…”
Section: Clc-3 and Endothelial Dysfunctionmentioning
confidence: 97%