首页> 外文期刊>The Journal of Physiology >Induction of betaine-gamma-aminobutyric acid transport activity in porcine chondrocytes exposed to hypertonicity.
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Induction of betaine-gamma-aminobutyric acid transport activity in porcine chondrocytes exposed to hypertonicity.

机译:暴露于高渗的猪软骨细胞中甜菜碱-γ-氨基丁酸转运活性的诱导。

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1. We measured the rates of uptake of selected amino acids and betaine by primary cultures of chondrocytes from porcine articular cartilage after the cells had been incubated in 'isotonic' (0.3 osmol l-1) or hypertonic (0.5 osmol l-1) media. 2. Na+-dependent uptake of methylaminoisobutyric acid increased rapidly when the cells were exposed to hypertonic conditions, reached a peak after 6-9 h, and then gradually decreased so that after 24 h it was only slightly above the control value. Conversely, (Na+ + Cl-)-dependent influx of gamma-aminobutyric acid (GABA) remained low for the first 9 h of hypertonic incubation, but then increased markedly to reach a plateau value after 24-30 h. Betaine influx also increased in cells incubated in hypertonic medium, being mainly Na+ dependent after 6 h, but (Na+ + Cl-)-dependent after 24 h. 3. This pattern indicates that exposure of the chondrocytes to hypertonicity induces first amino acid transport system A and then, as this decreases again, betaine-GABA transport activity. 4. Induction of betaine-GABA transport activity did not require continuous exposure of chondrocytes to hypertonicity; but the magnitude of the increase measured at the end of a 24 h incubation period was proportional to the length of time the cells had been exposed to hypertonicity during the 24 h. 5. Isolation and culture of chondrocytes in 0.4 osmol l-1 medium, instead of 0.3 osmol l-1, significantly increased their betaine-GABA transport activity, but not their system A activity. 6. Induction of betaine-GABA transport activity was prevented by addition of either actinomycin D or cycloheximide to the medium, but no mRNA for the betaine-GABA transporter known as BGT-1 was detected by Northern blot analysis of extracts of chondrocytes.
机译:1.在“等渗”(0.3 osmol l-1)或高渗(0.5 osmol l-1)培养基中孵育细胞后,我们测量了猪关节软骨软骨细胞原代培养物摄取所选氨基酸和甜菜碱的速率。 。 2.当细胞暴露于高渗条件下时,依赖于Na +的甲基氨基异丁酸吸收迅速增加,在6-​​9小时后达到峰值,然后逐渐下降,因此在24小时后仅略高于对照值。相反,在高渗温育的前9小时,γ-氨基丁酸(GABA)的(Na + + Cl-)依赖性流入量仍然很低,但在24-30小时后显着增加,达到平稳值。在高渗培养基中温育的细胞中,甜菜碱的流入量也增加,在6小时后主要依赖于Na +,但在24小时后依赖于(Na + + Cl-)。 3.这种模式表明,软骨细胞暴露于高渗状态会首先诱导氨基酸转运系统A,然后再降低甜菜碱-GABA转运活性。 4.诱导甜菜碱-GABA转运活性不需要将软骨细胞连续暴露于高渗性;但是在24小时孵育期结束时测得的增加幅度与细胞在24小时内暴露于高渗状态的时间长度成正比。 5.在0.4 osmol l-1培养基而不是0.3 osmol l-1中分离和培养软骨细胞,可显着增加其甜菜碱-GABA转运活性,但不增加其系统A活性。 6.通过向培养基中添加放线菌素D或环己酰亚胺来阻止甜菜碱-GABA转运活性的诱导,但是通过软骨细胞提取物的Northern印迹分析未检测到甜菜碱-GABA转运蛋白的BGT-1 mRNA。

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