Proinsulin C-peptide increases nitric oxide production by enhancing mitogen-activated protein-kinase-dependent transcription of endothelial nitric oxide synthase in aortic endothelial cells of Wistar rats

被引:86
|
作者
Kitamura, T
Kimura, K [1 ]
Makondo, K
Furuya, DT
Suzuki, M
Yoshida, T
Saito, M
机构
[1] Hokkaido Univ, Grad Sch Vet Med, Dept Biomed Sci, Biochem Lab, Sapporo, Hokkaido 0600818, Japan
[2] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Endocrinol & Metab, Kyoto, Japan
关键词
actinomycin D; C-peptide; endothelial cells; eNOS; ERK; L-NAME; MAPK; nitric oxide; p38MAPK; proinsulin;
D O I
10.1007/s00125-003-1232-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. Recent studies have suggested that proinsulin C-peptide improves vascular functions, possibly through nitric oxide (NO) production. To clarify the molecular mechanisms of vascular NO production induced by C-peptide, we examined the effects of C-peptide on NO production and NO synthase expression in rat aortic endothelial cells in connection with mitogen-activated protein kinase (MAPK) activation. Methods. Aortic endothelial cells were isolated from female Wistar rats, cultured to confluence, and serum-starved for 24 h before treatment with C-peptide. Nitric oxide production was measured by the DAF-2 fluorescence dye method and relative amounts of endothelial nitric oxide synthase (eNOS) protein and its mRNA were semi-quantified by western blot and RT-PCR analyses respectively. Activation of MAPK was estimated by western blot detection of activity-related phosphorylation and in vitro kinase assay. Results. Stimulation of cells with C-peptide for 3 h doubled NO production, which was suppressed by the NO synthase inhibitor, N-G-nitro-L-arginine methyl ester (L-NAME). Stimulation also increased mRNA and protein contents of eNOS in a manner sensitive to the transcription inhibitor actinomycin D. It did not affect inducible NO synthase mRNA. C-peptide also induced rapid phosphorylation and activation of extracellular signal-regulated kinase (ERK, also known as p44/42MAPK), but not of p38MAPK. In cells pretreated with the ERK inhibitor PD98059 the C-peptide-elicited increase of NO production and eNOS was abrogated in a dose-dependent manner; suppression of ERK phosphorylation induced by C-peptide also occurred. Conclusions/interpretation. Our results show that C-peptide increases NO production by increasing eNOS protein contents through ERK-dependent up-regulation of eNOS gene transcription. This could explain some actions of C-peptide on the vasculature, indicating a pivotal role for C-peptide in vascular homeostasis.
引用
收藏
页码:1698 / 1705
页数:8
相关论文
共 50 条
  • [41] Serotonin-induced activation of endothelial nitric oxide synthase and mitogen-activated protein kinase kinase:: Role of 5-hydroxytryptamine1B receptors.
    McDuffie, JE
    Maleque, MA
    FASEB JOURNAL, 1998, 12 (04): : A454 - A454
  • [42] Angiotensin II (AII) elevates endothelial nitric oxide synthase (eNOS) protein levels and activates mitogen-activated protein kinase (MAPK) in ovine feto-placental artery endothelial (OFAE) cells.
    Zheng, J
    Melsaether, AN
    Bird, IM
    Magness, RR
    BIOLOGY OF REPRODUCTION, 1998, 58 : 126 - 126
  • [43] SB 203580 inhibits p38 mitogen-activated protein kinase, nitric oxide production, and inducible nitric oxide synthase in bovine cartilage-derived chondrocytes
    Badger, AM
    Cook, MN
    Lark, MW
    Newman-Tarr, TM
    Swift, BA
    Nelson, AH
    Barone, FC
    Kumar, S
    JOURNAL OF IMMUNOLOGY, 1998, 161 (01): : 467 - 473
  • [44] Protein kinase C activation increases endothelial nitric oxide release in mesenteric arteries from orchidectomized rats
    Blanco-Rivero, Javier
    Sagredo, Ana
    Balfagon, Gloria
    Ferrer, Mercedes
    JOURNAL OF ENDOCRINOLOGY, 2007, 192 (01) : 189 - 197
  • [45] Role of mitogen-activated protein kinases (MAPK) in adenosine-A2 purinoceptor induced stimulation of human endothelial nitric oxide synthase
    Wyatt, A
    Sobrevia, L
    Wheeler-Jones, CPD
    Mann, GE
    JOURNAL OF VASCULAR RESEARCH, 1998, 35 : 43 - 43
  • [46] Inducible Nitric-oxide Synthase Expression Is Regulated by Mitogen-activated Protein Kinase Phosphatase-1
    Wang, Xianxi
    Zhao, Qun
    Matta, Ranyia
    Meng, Xiaomei
    Liu, Xiuping
    Liu, Chang-Gong
    Nelin, Leif D.
    Liu, Yusen
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (40) : 27123 - 27134
  • [47] Protein kinase C delta modulates endothelial nitric oxide synthase after cardiac arrest
    Lin, Hung Wen
    Gresia, Victoria L.
    Stradecki, Holly M.
    Alekseyenko, Aleksey
    Dezfulian, Cameron
    Neumann, Jake T.
    Dave, Kunjan R.
    Perez-Pinzon, Miguel A.
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2014, 34 (04): : 613 - 620
  • [48] Parathyroid hormone stimulates the endothelial nitric oxide synthase through protein kinase A and C pathways
    Rashid, Gloria
    Bernheim, Jacques
    Green, Janice
    Benchetrit, Sydney
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (10) : 2831 - 2837
  • [49] Ginsenoside Rg3 increases nitric oxide production via increases in phosphorylation and expression of endothelial nitric oxide synthase: Essential roles of estrogen receptor-dependent PI3-kinase and AMP-activated protein kinase
    Hien, Tran Thi
    Kim, Nak Doo
    Pokharel, Yuba Raj
    Oh, Seok Jeong
    Lee, Moo Yeol
    Kang, Keon Wook
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2010, 246 (03) : 171 - 183
  • [50] The effect of cigarette smoke on the phosphorylation of endothelial nitric oxide synthase: Role of protein kinase C
    Wagner, Laszlo
    Laczy, Boglarka
    Tamasko, Monika
    Mazak, Istvan
    Marko, Lajos
    Molnar, Gergo
    Wagner, Zoltan
    Mohas, Marton
    Cseh, Judit
    Fekete, Andrea
    Wittmann, Istvan
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 : 243 - 244