The substitution of SERCA2 redox cysteine 674 promotes pulmonary vascular remodeling by activating IRE1α/XBP1s pathway.
10.1016/j.apsb.2021.12.025
- Author:
Weimin YU
1
;
Gang XU
2
;
Hui CHEN
1
;
Li XIAO
1
;
Gang LIU
1
;
Pingping HU
1
;
Siqi LI
1
;
Vivi KASIM
3
;
Chunyu ZENG
4
;
Xiaoyong TONG
1
Author Information
1. School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China.
2. Institute of Medicine and Equipment for High Altitude Region, College of High Altitude Military Medicine, Army Medical University (Third Military Medical University), Chongqing 400038, China.
3. Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.
4. Department of Cardiology, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing 400042, China.
- Publication Type:Journal Article
- Keywords:
Endoplasmic reticulum stress;
Oxidative stress;
Pulmonary artery smooth muscle cell;
Pulmonary hypertension;
Pulmonary vascular remodeling;
Sarcoplasmic/endoplasmic reticulum Ca2+ ATPase
- From:
Acta Pharmaceutica Sinica B
2022;12(5):2315-2329
- CountryChina
- Language:English
-
Abstract:
Pulmonary hypertension (PH) is a life-threatening disease characterized by pulmonary vascular remodeling, in which hyperproliferation of pulmonary artery smooth muscle cells (PASMCs) plays an important role. The cysteine 674 (C674) in the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase 2 (SERCA2) is the critical redox regulatory cysteine to regulate SERCA2 activity. Heterozygous SERCA2 C674S knock-in mice (SKI), where one copy of C674 was substituted by serine to represent partial C674 oxidative inactivation, developed significant pulmonary vascular remodeling resembling human PH, and their right ventricular systolic pressure modestly increased with age. In PASMCs, substitution of C674 activated inositol requiring enzyme 1 alpha (IRE1α) and spliced X-box binding protein 1 (XBP1s) pathway, accelerated cell cycle and cell proliferation, which reversed by IRE1α/XBP1s pathway inhibitor 4μ8C. In addition, suppressing the IRE1α/XBP1s pathway prevented pulmonary vascular remodeling caused by substitution of C674. Similar to SERCA2a, SERCA2b is also important to restrict the proliferation of PASMCs. Our study articulates the causal effect of C674 oxidative inactivation on the development of pulmonary vascular remodeling and PH, emphasizing the importance of C674 in restricting PASMC proliferation to maintain pulmonary vascular homeostasis. Moreover, the IRE1α/XBP1s pathway and SERCA2 might be potential targets for PH therapy.
