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CA II 缺陷小鼠大脑中与膜相关的碳酸酐酶活性

Membrane-associated carbonic anhydrase activity in the brain of CA II-deficient mice.

作者信息

Ridderstråle Y, Wistrand P J

机构信息

Department of Animal Physiology, Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

J Neurocytol. 2000 Apr;29(4):263-9. doi: 10.1023/a:1026571704422.

Abstract

Membrane-associated carbonic anhydrase (CA) activity is of importance for transepithelial transport of ions and fluid. Histochemical studies have indicated its presence in the brain, but the data are difficult to evaluate because of interference from cytoplasmic CA isozymes, of which CA II is the predominant one. CA II-deficient mice offer a possibility to study the location of membrane-associated CA-activity, without interference from CA II. The location of CA activity in the brain of CA II-deficient and normal mice was studied by the cobalt-phosphate histochemical method, and that of CA I, CA II and CA III by an immunocytochemical method. The brains of both types of mice lacked cytoplasmic isozymes CA I and CA III, and the CA II-deficient mice also lacked CA II. In the normal mice, oligodendrocytes and choroid epithelium stained for CA II in the cytoplasm. In normal and CA (II)D-mice there was an intense membrane associated histochemical CA activity in neuronal processes. Neuronal perikarya were not stained. Endothelial membranes of brain capillaries showed strong histochemical CA-activity. Choroid epithelial cells had histochemical CA activity in the cytoplasm and along apical and baso-lateral cell membranes. The results suggest that membrane-associated CA-activity found along neuronal processes probably modulates pH of the extracellular fluid and thus neuronal activity. CA II and the membrane-associated CA of choroidal epithelium are probably involved in the secretion of cerebrospinal fluid.

摘要

膜相关碳酸酐酶(CA)活性对于离子和液体的跨上皮运输至关重要。组织化学研究表明其存在于大脑中,但由于细胞质CA同工酶的干扰,数据难以评估,其中CA II是主要的同工酶。CA II缺陷小鼠提供了一个研究膜相关CA活性位置的机会,而不受CA II的干扰。通过磷酸钴组织化学方法研究了CA II缺陷小鼠和正常小鼠大脑中CA活性的位置,并通过免疫细胞化学方法研究了CA I、CA II和CA III的位置。两种类型小鼠的大脑均缺乏细胞质同工酶CA I和CA III,CA II缺陷小鼠也缺乏CA II。在正常小鼠中,少突胶质细胞和脉络膜上皮细胞的细胞质中CA II染色。在正常小鼠和CA(II)D小鼠中,神经元突起中有强烈的膜相关组织化学CA活性。神经元胞体未染色。脑毛细血管的内皮膜显示出强烈的组织化学CA活性。脉络膜上皮细胞在细胞质以及顶端和基底外侧细胞膜上具有组织化学CA活性。结果表明,在神经元突起中发现的膜相关CA活性可能调节细胞外液的pH值,从而调节神经元活性。CA II和脉络膜上皮的膜相关CA可能参与脑脊液的分泌。

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