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mTORC1 Is Involved in Hypoxia‐Induced Pulmonary Hypertension Through the Activation of Notch3
Author(s) -
Wang Wang,
Liu Jie,
Ma Aiping,
Miao Ran,
Jin Yuling,
Zhang Hongbing,
Xu Kaifeng,
Wang Chen,
Wang Jun
Publication year - 2014
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.24670
Subject(s) - mtorc1 , pi3k/akt/mtor pathway , hypoxia (environmental) , right ventricular hypertrophy , pulmonary hypertension , pharmacology , mtorc2 , muscle hypertrophy , lung , medicine , signal transduction , chemistry , endocrinology , biology , microbiology and biotechnology , organic chemistry , oxygen
Hypoxia‐induced pulmonary hypertension (HPH) is a clinical syndrome associated with high morbidity and mortality. However, the underlying mechanisms remain unclear. Both the mammalian target of rapamycin (mTOR) and the Notch3 signaling pathways have been reported to be involved in HPH; however, it is unknown whether there is a connection between these two signaling pathways in HPH. This study was designed to investigate the relationship between mTOR and Notch3 in HPH. After treatment with 10% O 2 for 4 weeks, male C57BL/6 mice developed HPH with gradually increased right ventricular systolic pressure (RVSP), right ventricular hypertrophy index (RVHI), and pulmonary arteriolar remodeling accompanied by the activation of mTOR complex 1 (mTORC1) and Notch3 in the lung tissue and pulmonary arterioles. Pretreatment with the mTORC1 inhibitor rapamycin not only alleviated pulmonary arterial pressure and pulmonary arteriolar remodeling but also suppressed hypoxia‐induced mTORC1 and Notch3 activation. Prophylactic N ‐[ N ‐(3,5‐difluorophenacetyl)‐ L ‐alanyl]‐ S ‐phenylglycine t ‐butyl ester (DAPT) administration, a Notch signaling inhibitor, protected against the effects of hypoxia. These in vivo data were confirmed by in vitro experiments on human pulmonary arterial smooth muscle cell (PASMC) exposed to 3% O 2 . Furthermore, overexpression of Notch3 intracellular domain partially abrogated the inhibitory effects of rapamycin on human PASMC proliferation. These data indicate that both mTORC1 and Notch3 signaling are involved in HPH and the downstream effects of mTORC1 activation in HPH are partially dependent on the activation of Notch3 signaling. J. Cell. Physiol. 229: 2117–2125, 2014. © 2014 Wiley Periodicals, Inc.