| First Author | Liu X | Year | 2019 |
| Journal | Biochem Biophys Res Commun | Volume | 508 |
| Issue | 4 | Pages | 1202-1208 |
| PubMed ID | 30554656 | Mgi Jnum | J:291842 |
| Mgi Id | MGI:6443186 | Doi | 10.1016/j.bbrc.2018.12.064 |
| Citation | Liu X, et al. (2019) Cyclophilin D deficiency protects against the development of mitochondrial ROS and cellular inflammation in aorta. Biochem Biophys Res Commun 508(4):1202-1208 |
| abstractText | INTRODUCTION: Inflammation and oxidative stress are closely correlated in the pathology of cardiovascular disease. Mitochondrial cyclophilin D (CypD), the important modulator for mPTP opening, is increasingly recognized as a key regulator of cellular ROS generation. Besides, its association with cell inflammation is also being discovered. However, the effects of CypD in modulating vascular inflammatory response is unknown. We sought to investigate whether CypD deficiency attenutes vascular inflammation under physical conditions. METHODS AND RESULTS: We adopted CypD KO mouse and their littermate controls to observe the effects of CypD deficiency on aortic mitochondrial functions and vascular inflammation. As we found in our study, we confirmed that under physical conditions, CypD deficiency enhanced mouse whole body metabolic status, increased aortic mitochondrial complex III activity and decreased mitochondrial ROS generation. Functionally, CypD deficiency also attenuated inflammatory molecules expression, including VCAM-1, IL-6 and TNF-alpha in mouse aorta. CONCLUSIONS: Our results review that mitochondrial CypD is involved in the regulation of inflammation in aorta and provide insights that blocking mitochondrial CypD enhances vascular resistance to inflammatory injuries. |
