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牛晶状体上皮细胞肌醇摄取的渗透调节改变。第4部分:高渗条件下Na(+)-肌醇共转运体mRNA的诱导模式,表明存在针对水分胁迫的早期、相互作用的保护机制。

Osmoregulatory alterations in myo-inositol uptake by bovine lens epithelial cells. Part 4: Induction pattern of Na(+)-myo-inositol cotransporter mRNA under hypertonic conditions denoting an early-onset, interactive, protective mechanism against water stress.

作者信息

Zhou C, Chen H Q, Reeves R, Agarwal N, Cammarata P R

机构信息

Department of Anatomy and Cell Biology, University of North Texas Health Science Center at Fort Worth/North Texas Eye Research Institute 76107.

出版信息

Invest Ophthalmol Vis Sci. 1994 Nov;35(12):4118-25.

PMID:7960594
Abstract

PURPOSE

To examine the effect of hypertonicity on the induction of the Na(+)-myo-inositol (Na(+)-MI) cotransporter(s) in cultured bovine lens epithelial cells (BLECs).

METHODS

Na(+)-MI cotransporter 626-bp reverse transcription-polymerase chain reaction product amplified from lens cell RNA and aldose reductase (AR) cDNA probes were used to measure respective mRNA content by Northern blot analysis.

RESULTS

Northern blot analysis of BLEC mRNA hybridized to Na(+)-MI cotransporter cDNA showed that Na(+)-MI cotransporter mRNA increased when secondary cultures of BLECs were exposed to physiological medium supplemented with 116 mmol/l NaCl. A time course further revealed a maximal increase in Na(+)-MI cotransporter mRNA by 8 hours. Thereafter, the level of Na(+)-MI cotransporter mRNA steadily declined for the duration of the 72-hour incubation period despite continuous exposure of BLECs to hypertonicity. AR mRNA levels maximally increased by 24 h of cell exposure to hypertonic condition. Unlike Na(+)-MI cotransporter mRNA, AR mRNA remained elevated throughout the duration of the experiment. Hypertonic exposure resulted in a steady state accumulation of myo-inositol and sorbitol for 6 days. Inhibition of sorbitol formation prompted the intracellular myo-inositol content to a higher level.

CONCLUSIONS

These data suggest that enhanced MI transport and accumulation, as an adaptive osmoregulatory response to hypertonicity in cultured BLECs, is a primary, early-onset, protective mechanism against water stress, succeeded by, enhanced sorbitol formation and accumulation, a secondary, late-onset protective mechanism. The lens appears to respond to the preliminary stages of hyperosmotic stress by induction of Na(+)-MI cotransporter mRNA, indicating that the myo-inositol carrier protein(s) play an initial responsive role in the management of osmotic stress. Lens water stress management is interactive because myo-inositol and sorbitol levels are regulated in concert.

摘要

目的

研究高渗对培养的牛晶状体上皮细胞(BLECs)中钠-肌醇(Na(+)-MI)共转运体诱导的影响。

方法

从晶状体细胞RNA中扩增出的626bp钠-肌醇共转运体逆转录-聚合酶链反应产物和醛糖还原酶(AR)cDNA探针,用于通过Northern印迹分析测量各自的mRNA含量。

结果

与钠-肌醇共转运体cDNA杂交的BLEC mRNA的Northern印迹分析表明,当BLECs的传代培养物暴露于补充有116mmol/l NaCl的生理培养基中时,钠-肌醇共转运体mRNA增加。时间进程进一步显示,钠-肌醇共转运体mRNA在8小时时最大增加。此后,尽管BLECs持续暴露于高渗环境,但在72小时的孵育期内,钠-肌醇共转运体mRNA水平稳步下降。细胞暴露于高渗条件24小时时,AR mRNA水平最大增加。与钠-肌醇共转运体mRNA不同,AR mRNA在整个实验过程中一直保持升高。高渗暴露导致肌醇和山梨醇稳定积累6天。山梨醇形成的抑制促使细胞内肌醇含量达到更高水平。

结论

这些数据表明,在培养的BLECs中,作为对高渗的适应性渗透调节反应,增强的肌醇转运和积累是对抗水分胁迫的主要、早期发生的保护机制,随后是增强的山梨醇形成和积累,这是次要的、晚期发生的保护机制。晶状体似乎通过诱导钠-肌醇共转运体mRNA对高渗应激的初始阶段作出反应,表明肌醇载体蛋白在渗透应激管理中起初始反应作用。晶状体水分胁迫管理是相互作用的,因为肌醇和山梨醇水平是协同调节的。

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