Sakai Masashi, Tamura Kouichi, Tsurumi Yuko, Tanaka Yutaka, Koide Yuichi, Matsuda Miyuki, Ishigami Tomoaki, Yabana Machiko, Tokita Yasuo, Hiroi Yukio, Komuro Issei, Umemura Satoshi
Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Am J Physiol Renal Physiol. 2007 May;292(5):F1526-36. doi: 10.1152/ajprenal.00451.2006. Epub 2007 Feb 13.
MAK-V/Hunk is an SNF1-related serine/threonine kinase which was previously shown to be highly expressed in the mammary gland and central nervous system. In this study, we found MAK-V/Hunk is abundantly and specifically expressed in the thick ascending limbs and distal convoluted tubules (DCT) of the kidney from the embryonic stage to the adult stage. We demonstrated that dietary salt depletion significantly enhances renal MAK-V/Hunk mRNA levels compared with a normal-salt diet. To analyze the possible renal cellular function of this kinase, we employed mouse distal convoluted tubule (mDCT) cells. The results of reverse transcriptase-polymerase chain reaction and Western blot analysis revealed that MAK-V/Hunk is expressed endogenously in mDCT cells. Overexpression of MAK-V/Hunk by adenoviral gene transfer significantly inhibited the ANG II-induced stimulation of c-fos gene transcription and suppressed the ANG II-mediated increases in transforming growth factor-beta production into the medium. This phenomenon was accompanied by inhibition of ANG II-induced activation of BrdU incorporation. On the other hand, the MAK-V/Hunk knockdown by siRNA activated the ANG II-induced c-fos gene expression. In the consecutive sections stained for MAK-V/Hunk and AT(1) receptor, MAK-V/Hunk-immunopositive distal tubules expressed the AT(1) receptor. This is the first report on the intrarenal localization of MAK-V/Hunk and its cellular function in renal tubular cells.
MAK-V/Hunk是一种与SNF1相关的丝氨酸/苏氨酸激酶,先前已证明其在乳腺和中枢神经系统中高表达。在本研究中,我们发现MAK-V/Hunk从胚胎期到成年期在肾脏的髓袢升支粗段和远曲小管(DCT)中大量且特异性表达。我们证明,与正常盐饮食相比,饮食中盐缺乏显著提高了肾脏MAK-V/Hunk mRNA水平。为了分析这种激酶可能的肾脏细胞功能,我们使用了小鼠远曲小管(mDCT)细胞。逆转录聚合酶链反应和蛋白质印迹分析结果显示,MAK-V/Hunk在mDCT细胞中内源性表达。通过腺病毒基因转移过表达MAK-V/Hunk可显著抑制血管紧张素II诱导的c-fos基因转录刺激,并抑制血管紧张素II介导的培养基中转化生长因子-β产生的增加。这种现象伴随着血管紧张素II诱导的BrdU掺入激活的抑制。另一方面,通过小干扰RNA敲低MAK-V/Hunk可激活血管紧张素II诱导的c-fos基因表达。在连续切片上对MAK-V/Hunk和AT(1)受体进行染色,MAK-V/Hunk免疫阳性的远曲小管表达AT(1)受体。这是关于MAK-V/Hunk在肾脏内的定位及其在肾小管细胞中的细胞功能的首次报道。