Abstract | BACKGROUND: METHODS: PH was induced by exposing wild-type (WT) mice and TfR1 hetero knockout mice to hypoxia for 4 weeks and evaluated via assessment of pulmonary vascular remodeling, right ventricular (RV) systolic pressure, and RV hypertrophy. In addition, we assessed the functional role of TfR1 in pulmonary artery smooth muscle cells in vitro. RESULTS: The morphology of pulmonary arteries did not differ between WT mice and TfR1 hetero knockout mice under normoxic conditions. In contrast, TfR1 hetero knockout mice exposed to 4 weeks hypoxia showed attenuated pulmonary vascular remodeling, RV systolic pressure, and RV hypertrophy compared with WT mice. In addition, the depletion of TfR1 by RNA interference attenuated human pulmonary artery smooth muscle cells proliferation induced by platelet-derived growth factor-BB ( PDGF-BB) in vitro. CONCLUSIONS:
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Authors | Yoshiro Naito, Manami Hosokawa, Hisashi Sawada, Makiko Oboshi, Shinichi Hirotani, Toshihiro Iwasaku, Yoshitaka Okuhara, Daisuke Morisawa, Akiyo Eguchi, Koichi Nishimura, Yuko Soyama, Kenichi Fujii, Toshiaki Mano, Masaharu Ishihara, Takeshi Tsujino, Tohru Masuyama |
Journal | American journal of hypertension
(Am J Hypertens)
Vol. 29
Issue 6
Pg. 713-8
(06 2016)
ISSN: 1941-7225 [Electronic] United States |
PMID | 26419445
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © American Journal of Hypertension, Ltd 2015. All rights reserved. For Permissions, please email: [email protected]. |
Chemical References |
- Receptors, Transferrin
- Tfrc protein, mouse
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Topics |
- Animals
- Hypertension, Pulmonary
(pathology, physiopathology)
- Hypoxia
(physiopathology)
- Male
- Mice, Knockout
- Myocytes, Smooth Muscle
(physiology)
- Pulmonary Artery
(pathology)
- Receptors, Transferrin
(physiology)
- Vascular Remodeling
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