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哺乳动物卵母细胞的膜转运特性:一种微吸管灌注技术。

Membrane transport properties of mammalian oocytes: a micropipette perfusion technique.

作者信息

Gao D Y, McGrath J J, Tao J, Benson C T, Critser E S, Critser J K

机构信息

Cryobiology Research Institute, Methodist Hospital of Indiana, Indianapolis 46202.

出版信息

J Reprod Fertil. 1994 Nov;102(2):385-92. doi: 10.1530/jrf.0.1020385.

Abstract

A perfusion technique using micropipette methodology was developed to determine quantitatively the membrane transport properties of mammalian oocytes. This method eliminates modelling ambiguities inherent in microdiffusion, a closely related technology, and should prove to be especially valuable for study of the coupled transport of water and cryoprotectant through mammalian oocytes and embryos. The method is described and evidence given for validity of the method for the simple case of uncoupled flow of water through the mouse oocyte membrane. The zona pellucida of a mouse oocyte was held by a micropipette with an 8-10 microns diameter tip opening and perfused by hyperosmotic media. The kinetic volume change of the cell was videotaped and quantified by image analysis. Experimental data and mathematical modelling were used to determine the hydraulic conductivity of the oocyte membrane (Lp) found to be 1.05, 0.45 and 0.26 microns min-1 atm-1 at 30 degrees C, 22 degrees C and 12 degrees C, respectively. The corresponding activation energy, Ea, for Lp was calculated to be 13.0 kcal mol-1. These values are in agreement with data obtained by other techniques. One of the major advantages of this technique is that the extracellular osmotic condition can be changed readily by perfusing a single cell with a prepared medium. To study the response of the same cell to different osmotic conditions, the old perfusion medium can be removed easily and the cell reperfused with a different medium.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一种使用微量移液器方法的灌注技术被开发出来,用于定量测定哺乳动物卵母细胞的膜转运特性。该方法消除了微扩散(一种密切相关的技术)中固有的建模模糊性,并且对于研究水和冷冻保护剂通过哺乳动物卵母细胞和胚胎的耦合转运应该特别有价值。本文描述了该方法,并给出了该方法在水通过小鼠卵母细胞膜的简单非耦合流动情况下有效性的证据。用直径为8 - 10微米的微量移液器吸头夹住小鼠卵母细胞的透明带,并用高渗介质进行灌注。通过图像分析对细胞的动态体积变化进行录像和定量。利用实验数据和数学模型确定卵母细胞膜的水力传导率(Lp),发现在30℃、22℃和12℃时分别为1.05、0.45和0.26微米·分钟⁻¹·大气压⁻¹。计算出Lp的相应活化能Ea为13.0千卡·摩尔⁻¹。这些值与通过其他技术获得的数据一致。该技术的一个主要优点是,通过用制备好的介质灌注单个细胞,可以很容易地改变细胞外的渗透条件。为了研究同一个细胞对不同渗透条件的反应,可以很容易地去除旧的灌注介质,并用不同的介质对细胞进行重新灌注。(摘要截于250字)

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