Anti-oxidative effect of Klotho on endothelial cells through cAMP activation

被引:106
作者
Rakugi, Hiromi
Matsukawa, Naomichi
Ishikawa, Kazuhiko
Yang, Jin
Imai, Michio
Ikushima, Masashi
Maekawa, Yoshihiro
Kida, Iwao
Miyazaki, Jun-Ichi
Ogihara, Toshio
机构
[1] Osaka Univ, Grad Sch Med, Dept Geriatr Med, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Div Stem Cell Regulat Res, Suita, Osaka, Japan
关键词
aging; angiotensin; antioxidants; endothelium; klotho;
D O I
10.1007/s12020-007-0016-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Klotho, a regulatory factor implicated in countering the aging process, has been reported to ameliorate endothelial dysfunction in vivo. To clarify whether Klotho protein directly affects endothelial cell function, we studied the effects of membrane-form Klotho on manganese superoxide dismutase (Mn-SOD) expression and nitric oxide production in human umbilical vein endothelial cells (HUVEC). We incubated HUVEC with conditioned medium from COS-1 cells transfected with expression vector, pCAGGS-klotho (Klotho-CM) or a recombinant, purified 6His-tagged Klotho protein. Both Klotho-CM and 6His-tagged Klotho protein enhanced Mn-SOD expression by approximately two-fold, partially via activation of the cAMP signaling pathway. Furthermore, Klotho-CM increased nitric oxide production, which also contributed to the up-regulation of Mn-SOD. Using the oxidation-sensitive dye dihydroethidium, we found that Klotho inhibited angiotensin II-induced reactive oxygen species production in HUVEC. These findings provide new insights into the mechanisms of Klotho action and support the therapeutic potential of membrane-form Klotho to regulate endothelial function.
引用
收藏
页码:82 / 87
页数:6
相关论文
共 34 条
[1]   Preconditioning-mediated neuroprotection - Role of nitric oxide, cGMP, and new protein expression [J].
Andoh, T ;
Chock, PB ;
Chiueh, CC .
NITRIC OXIDE: NOVEL ACTIONS, DELETERIOUS EFFECTS AND CLINICAL POTENTIAL, 2002, 962 :1-7
[2]   Association of human aging with a functional variant of Klotho [J].
Arking, DE ;
Krebsova, A ;
Macek, M ;
Macek, M ;
Arking, A ;
Mian, IS ;
Fried, L ;
Hamosh, A ;
Dey, S ;
McIntosh, I ;
Dietz, HC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :856-861
[3]   Shear stress stimulates phosphorylation of eNOS at Ser635 by a protein kinase A-dependent mechanism [J].
Boo, YC ;
Hwang, J ;
Sykes, M ;
Michell, BJ ;
Kemp, BE ;
Lum, H ;
Jo, H .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (05) :H1819-H1828
[4]   Shear stress stimulates phosphorylation of endothelial nitric-oxide synthase at Ser1179 by Akt-independent mechanisms -: Role of protein kinase A [J].
Boo, YC ;
Sorescu, G ;
Boyd, N ;
Shiojima, L ;
Walsh, K ;
Du, J ;
Jo, HJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3388-3396
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   Identification of copper zinc superoxide dismutase as a novel nitric oxide-regulated gene in rat glomerular mesangial cells and kidneys of endotoxemic rats [J].
Frank, S ;
Zacharowski, K ;
Wray, GM ;
Thiemermann, C ;
Pfeilschifter, J .
FASEB JOURNAL, 1999, 13 (08) :869-882
[7]   Regulation of the vascular extracellular superoxide dismutase by nitric oxide and exercise training [J].
Fukai, T ;
Siegfried, MR ;
Ushio-Fukai, M ;
Cheng, Y ;
Kojda, G ;
Harrison, DG .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (11) :1631-1639
[8]   Nifedipine indirectly upregulates superoxide dismutase expression in endothelial cells via vascular smooth muscle cell-dependent pathways [J].
Fukuo, K ;
Yang, J ;
Yasuda, O ;
Mogi, M ;
Suhara, T ;
Sato, N ;
Suzuki, T ;
Morimoto, S ;
Ogihara, T .
CIRCULATION, 2002, 106 (03) :356-361
[9]   Anti-apoptotic and anti-senescence effects of Klotho on vascular endothelial cells [J].
Ikushima, M ;
Rakugi, H ;
Ishikawa, K ;
Maekawa, Y ;
Yamamoto, K ;
Ohta, J ;
Chihara, Y ;
Kida, I ;
Ogihara, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 339 (03) :827-832
[10]   Klotho protein activates the PKC pathway in the kidney and testis and suppresses 25-hydroxyvitamin D3 1α-hydroxylase gene expression [J].
Imai, M ;
Ishikawa, K ;
Matsukawa, N ;
Kida, I ;
Ohta, J ;
Ikushima, M ;
Chihara, Y ;
Rui, X ;
Rakugi, H ;
Ogihara, T .
ENDOCRINE, 2004, 25 (03) :229-234