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通过分离肝细胞的细胞质透析测定细胞内荧光阴离子的游离浓度。

Free concentrations of intracellular fluorescent anions determined by cytoplasmic dialysis of isolated hepatocytes.

作者信息

Weinman S A, Maglova L M

机构信息

Department of Internal Medicine, University of Texas Medical Branch, Galveston 77555-0641.

出版信息

Am J Physiol. 1994 Nov;267(5 Pt 1):G922-31. doi: 10.1152/ajpgi.1994.267.5.G922.

Abstract

Intracellular organic ions exist in free solution bound to cytoplasmic proteins, partitioned within intracellular membranes, and enclosed in intracellular vesicles and organelles. The aim of this study was to develop a method for measurement of the free cytosolic concentration of organic ions. This was accomplished by measuring initial rates of diffusion between patch-clamp pipettes and cell cytoplasm and determining the null-point concentration of this process. Carboxydimethylfluorescein (CF) was used as a model compound. It readily diffused between cytoplasm and pipette, and there was a linear relationship between concentration in the pipette and equilibrium cell fluorescence. When cells previously loaded with CF were patched, intracellular fluorescence rapidly changed in a positive or a negative direction, depending on the concentration of CF in the pipette. The null point, defined as the concentration at which cells neither gained nor lost fluorescence, described the same relationship between free concentration and total cell fluorescence as that determined by direct loading of the cells to equilibrium. In hepatocytes preloaded with a fluorescent bile acid derivative, cholylglycylamidofluorescein (CGamF), by exposure (0.05 microM) for 30 min, the null point occurred at a CGamF concentration in the pipette of 0.6 microM. This value is 12 times greater than that in the bath. In conclusion, a new method is described that can measure free cytosolic concentrations of fluorescent molecules. It should prove useful in determining the intracellular location and state of transported organic ions.

摘要

细胞内有机离子以游离溶液形式存在,与细胞质蛋白结合,分布于细胞内膜中,并被包裹在细胞内囊泡和细胞器中。本研究的目的是开发一种测量有机离子游离胞质浓度的方法。这是通过测量膜片钳吸管与细胞质之间的初始扩散速率,并确定该过程的零点浓度来实现的。羧基二甲基荧光素(CF)用作模型化合物。它很容易在细胞质和吸管之间扩散,吸管中的浓度与细胞平衡荧光之间存在线性关系。当对先前加载了CF的细胞进行膜片钳记录时,细胞内荧光会根据吸管中CF的浓度迅速向正向或负向变化。零点定义为细胞既不增加也不减少荧光的浓度,它描述了游离浓度与总细胞荧光之间的关系,与通过将细胞直接加载至平衡状态所确定的关系相同。在预先通过暴露(0.05 microM)30分钟加载了荧光胆汁酸衍生物胆酰甘氨酰胺荧光素(CGamF)的肝细胞中,吸管中CGamF浓度为0.6 microM时出现零点。该值比浴液中的值大12倍。总之,本文描述了一种可以测量荧光分子游离胞质浓度的新方法。它在确定转运有机离子的细胞内位置和状态方面应会很有用。

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