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The growth factor midkine regulates the renin-angiotensin system in mice
Akinori Hobo, … , Seiichi Matsuo, Kenji Kadomatsu
Akinori Hobo, … , Seiichi Matsuo, Kenji Kadomatsu
Published May 18, 2009
Citation Information: J Clin Invest. 2009;119(6):1616-1625. https://doi.org/10.1172/JCI37249.
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Research Article Nephrology

The growth factor midkine regulates the renin-angiotensin system in mice

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Abstract

The renin-angiotensin system plays a pivotal role in regulating blood pressure and is involved in the pathogenesis of kidney disorders and other diseases. Here, we report that the growth factor midkine is what we believe to be a novel regulator of the renin-angiotensin system. The hypertension induced in mice by 5/6 nephrectomy was accompanied by renal damage and elevated plasma angiotensin II levels and was ameliorated by an angiotensin-converting enzyme (ACE) inhibitor and an angiotensin receptor blocker. Notably, ACE activity in the lung, midkine expression in the lung, and midkine levels in the plasma were all increased after 5/6 nephrectomy. Exposure to midkine protein enhanced ACE expression in primary cultured human lung microvascular endothelial cells. Furthermore, hypertension was not induced and renal damage was less severe in midkine-deficient mice. Supplemental administration of midkine protein to midkine-deficient mice restored ACE expression in the lung and hypertension after 5/6 nephrectomy. Oxidative stress might be involved in midkine expression, since expression of NADH/NADPH oxidase–1, –2, and –4 was induced in the lung after 5/6 nephrectomy. Indeed, the antioxidative reagent tempol reduced midkine expression and plasma angiotensin II levels and consequently ameliorated hypertension. These results suggest that midkine regulates the renin-angiotensin system and mediates the kidney-lung interaction after 5/6 nephrectomy.

Authors

Akinori Hobo, Yukio Yuzawa, Tomoki Kosugi, Noritoshi Kato, Naoto Asai, Waichi Sato, Shoichi Maruyama, Yasuhiko Ito, Hiroyuki Kobori, Shinya Ikematsu, Akira Nishiyama, Seiichi Matsuo, Kenji Kadomatsu

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Figure 4

Effects of exogenous MK and PTN in Mdk–/– mice on blood pressure and ACE expression in the lung.

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Effects of exogenous MK and PTN in Mdk–/– mice on blood pressure and ACE...
(A) SBP was measured by the tail-cuff method at 0 and 2 weeks after 5/6 nephrectomy (n = 5). **P < 0.01 versus untreated Mdk–/– mice (0 weeks); #P < 0.01, rh-MK versus saline. rh-PTN, recombinant human PTN. (B) ACE expression in the lung of Mdk–/– mice treated with MK and saline. Western blot data are shown. (C) The data in B were quantified using densitometry and are presented as mean and SD. †P < 0.01. (D) ACE expression in the lung of Mdk–/– mice treated with rh-PTN and saline. Western blot data are shown. (E) The data in D were quantified using densitometry and are presented as mean and SD.

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