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大鼠肾脏远端肾单位中多种形式肌酸激酶的区室化

Compartmentation of multiple forms of creatine kinase in the distal nephron of the rat kidney.

作者信息

Friedman D L, Perryman M B

机构信息

Department of Medicine, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Biol Chem. 1991 Nov 25;266(33):22404-10.

PMID:1939264
Abstract

Creatine kinase enzymes are present in tissues such as muscle and brain to interconvert creatine phosphate and ADP, thus providing a system to interconnect energy production and utilization (Bessman, S. P., and Carpenter, C. L. (1985) Annu. Rev. Biochem. 54, 831-862). Creatine kinase isoenzymes in kidney have received little attention since kidney contains relatively low creatine kinase activity compared with muscle and brain and because there is disagreement regarding the identity of the specific isoforms expressed in kidney. Using a combination of chromatographic and immunological techniques, we have identified two isoforms of creatine kinase in rat kidney supernatants, B creatine kinase, and the non-sarcomeric form of the mitochondrial creatine kinase, which represent 82 and 15%, respectively, of the total creatine kinase activity in this tissue. The identity of the non-muscle form of the mitochondrial creatine kinase was confirmed by N-terminal sequence analysis and compared with recently published cDNA sequences (Haas, R. C., and Strauss, A. W. (1990) J. Biol. Chem. 265, 6921-6927). We prepared multiple antisera specific for each isoform using synthetic peptide immunogens based upon nonhomologous regions from the primary sequence of each creatine kinase isoform. Immunocytochemical results demonstrate that both creatine kinase isoforms are colocalized in the inner stripe of the outer medulla in tubules of the distal nephron. A similar distribution of creatine kinase isoforms was obtained when different layers of the renal cortex and medulla were examined for creatine kinase activity and isozyme content using nondenaturing electrophoresis. In general, the distribution of creatine kinase enzymes in kidney corresponds to the regions of greatest ATP utilization, oxygen consumption, and sodium transport. These results suggest a role for creatine kinase enzymes in the coupling of ion transport and oxidative phosphorylation in the distal nephron of the mammalian kidney.

摘要

肌酸激酶存在于肌肉和大脑等组织中,可使磷酸肌酸和二磷酸腺苷相互转化,从而提供一个连接能量产生和利用的系统(贝斯曼,S.P.,和卡彭特,C.L.(1985年)《生物化学年度评论》54卷,831 - 862页)。肾脏中的肌酸激酶同工酶很少受到关注,因为与肌肉和大脑相比,肾脏中的肌酸激酶活性相对较低,而且对于肾脏中表达的特定同工型的身份存在分歧。通过结合色谱和免疫技术,我们在大鼠肾脏上清液中鉴定出了两种肌酸激酶同工型,即B肌酸激酶和线粒体肌酸激酶的非肌节形式,它们分别占该组织总肌酸激酶活性的82%和15%。通过N端序列分析证实了线粒体肌酸激酶非肌肉形式的身份,并与最近发表的cDNA序列进行了比较(哈斯,R.C.,和施特劳斯,A.W.(1990年)《生物化学杂志》265卷,6921 - 6927页)。我们使用基于每种肌酸激酶同工型一级序列非同源区域的合成肽免疫原制备了针对每种同工型的多种抗血清。免疫细胞化学结果表明,两种肌酸激酶同工型共定位于远曲小管外髓质的内带。当使用非变性电泳检查肾皮质和髓质的不同层的肌酸激酶活性和同工酶含量时,也获得了类似的肌酸激酶同工型分布。一般来说,肾脏中肌酸激酶的分布与最大ATP利用、氧气消耗和钠转运的区域相对应。这些结果表明肌酸激酶在哺乳动物肾脏远曲小管的离子转运和氧化磷酸化偶联中发挥作用。

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