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人类碳酸酐酶同工酶遗传性缺陷在理解其细胞作用方面的价值。

The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular roles.

作者信息

Tashian R E, Hewett-Emmett D, Dodgson S J, Forster R E, Sly W S

出版信息

Ann N Y Acad Sci. 1984;429:262-75. doi: 10.1111/j.1749-6632.1984.tb12346.x.

Abstract

Very little light has been shed on the role of the low-activity CA I isozyme in humans by studies on CA I-deficient individuals. On the other hand, CA II-deficient individuals exhibit abnormalities of bone, kidney and brain, implicating a functional role for the high-activity CA II isozyme in cells from these tissues and organs. It also appears that the CA II-deficient red cell is capable of normal respiratory function under unstressed conditions. In addition, there is some preliminary evidence that those organs such as the eye which primarily contain the CA II isozyme, may be able to function effectively in the absence of CA II.

摘要

对缺乏碳酸酐酶I(CA I)的个体进行的研究,很少能揭示低活性CA I同工酶在人类中的作用。另一方面,缺乏碳酸酐酶II(CA II)的个体表现出骨骼、肾脏和大脑的异常,这表明高活性CA II同工酶在这些组织和器官的细胞中具有功能作用。此外,在无应激条件下,缺乏CA II的红细胞似乎能够正常发挥呼吸功能。另外,有一些初步证据表明,那些主要含有CA II同工酶的器官,如眼睛,在没有CA II的情况下可能仍能有效发挥功能。

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