Suzuki E, Hirata Y, Hayakawa H, Omata M, Kojima M, Kangawa K, Minamino N, Matsuo H
Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1993 Apr 30;192(2):532-8. doi: 10.1006/bbrc.1993.1448.
To elucidate the physiological role of C-type natriuretic peptide (CNP) as a local mediator, we examined the production of CNP in the rat kidney. The content of CNP in the kidney was 0.47 +/- 0.02 [SE] fmol/mg wet weight and the major molecular form of CNP was CNP-53. An established cell line from the rat kidney, NRK-52E cell, secreted CNP at a rate of 9.15 +/- 0.96 fmol/24 hr/mg protein. Furthermore, CNP mRNA was detected in the rat kidney and NRK-52E cell utilizing reverse transcription-polymerase chain reaction (RT-PCR). On the other hand, ANP in the rat kidney (2.56 +/- 0.19 fmol/mg wet weight) had the molecular form of alpha-ANP, but ANP mRNA was not detected by RT-PCR. No BNP immunoreactivity was found in the rat kidney, although BNP mRNA was detected by RT-PCR. These results indicate that only CNP among the natriuretic peptides is produced in significant amounts in the rat kidney under normal physiological conditions and that renal parenchymal cells may produce CNP.
为阐明C型利钠肽(CNP)作为局部介质的生理作用,我们检测了大鼠肾脏中CNP的产生情况。肾脏中CNP的含量为0.47±0.02[标准误]fmol/mg湿重,且CNP的主要分子形式为CNP-53。从大鼠肾脏建立的细胞系NRK-52E细胞以9.15±0.96 fmol/24小时/毫克蛋白的速率分泌CNP。此外,利用逆转录-聚合酶链反应(RT-PCR)在大鼠肾脏和NRK-52E细胞中检测到了CNP mRNA。另一方面,大鼠肾脏中的心房钠尿肽(ANP,2.56±0.19 fmol/mg湿重)具有α-ANP的分子形式,但通过RT-PCR未检测到ANP mRNA。尽管通过RT-PCR检测到了脑钠肽(BNP)mRNA,但在大鼠肾脏中未发现BNP免疫反应性。这些结果表明,在正常生理条件下,利钠肽中只有CNP在大鼠肾脏中大量产生,且肾实质细胞可能产生CNP。