Exosomal non-coding RNAs: key regulators of inflammation-related cardiovascular disorders

被引:1
作者
Saadh, Mohamed J. [1 ]
Muhammad, Faris Anad [2 ]
Albadr, Rafid Jihad [3 ]
Sanghvi, Gaurav [4 ]
Ballal, Suhas [5 ]
Pathak, Piyus Kumar [6 ]
Bareja, Lakshay [7 ]
Aminov, Zafar [8 ]
Taher, Waam Mohammed [9 ]
Alwan, Mariem [10 ]
Jawad, Mahmood Jasem [11 ]
Al-Nuaimi, Ali M. Ali [12 ]
机构
[1] Middle East Univ, Fac Pharm, Amman 11831, Jordan
[2] Alnoor Univ, Coll Pharm, Nineveh, Iraq
[3] Ahl Al Bayt Univ, Kerbala, Iraq
[4] Marwadi Univ, Marwadi Univ Res Ctr, Fac Sci, Dept Microbiol, Rajkot 360003, Gujarat, India
[5] JAIN Univ, Sch Sci, Dept Chem & Biochem, Bangalore, Karnataka, India
[6] NIMS Univ Rajasthan, NIMS Inst Engn & Technol, Dept Appl Sci Chem, Jaipur, India
[7] Chitkara Univ, Chitkara Univ Inst Engn & Technol, Ctr Res Impact & Outcome, Rajpura 140401, Punjab, India
[8] Samarkand State Med Univ, Dept Publ Hlth & Healthcare Management, 18 Amir Temur St, Samarkand, Uzbekistan
[9] Natl Univ Sci & Technol, Coll Nursing, Dhi Qar, Iraq
[10] Al Farahidi Univ, Pharm Coll, Baghdad, Iraq
[11] Al Zahrawi Univ Coll, Dept Pharm, Karbala, Iraq
[12] Gilgamesh Ahliya Univ, Baghdad, Iraq
关键词
Cardiovascular disease; Inflammation; Exosome; MicroRNA; LncRNA; NF-KAPPA-B; HUMAN EPIGENOME CONSORTIUM; DEPENDENT PROTEIN-KINASE; SMOOTH-MUSCLE-CELLS; EXTRACELLULAR VESICLES; MYOCARDIAL-INFARCTION; CARDIAC DYSFUNCTION; ENDOTHELIAL-CELLS; IN-VITRO; HEART;
D O I
10.1186/s40001-025-02649-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Inflammation is a complex, tightly regulated process involving biochemical and cellular reactions to harmful stimuli. Often termed "the internal fire", it is crucial for protecting the body and facilitating tissue healing. While inflammation is essential for survival, chronic inflammation can be detrimental, leading to tissue damage and reduced survival. The innate immune system triggers inflammation, closely linked to the development of heart diseases, with significant consequences for individuals. Inflammation in arterial walls or the body substantially contributes to atherosclerotic disease progression, affecting the cardiovascular system. Altered lipoproteins increase the risk of excessive blood clotting, a hallmark of atherosclerotic cardiovascular disease and its complications. Integrating inflammatory biomarkers with established risk assessment techniques can enhance our ability to identify at-risk individuals, assess their risk severity, and recommend appropriate CVD prevention strategies. Exosomes, a type of extracellular vesicle, are released by various cells and mediate cell communication locally and systemically. In the past decade, exosomes have been increasingly studied for their vital roles in health maintenance and disease processes. They can transport substances like non-coding RNAs, lipids, and proteins between cells, influencing immune responses and inflammation to elicit harmful or healing effects. This study focuses on the critical role of inflammation in heart disease progression and how non-coding RNAs in exosomes modulate the inflammatory process, either exacerbating or alleviating inflammation-related damage in the cardiovascular system.
引用
收藏
页数:20
相关论文
共 206 条
[91]   Exosomes derived from mesenchymal stem cells attenuate the progression of atherosclerosis in ApoE-/- mice via miR-let7 mediated infiltration and polarization of M2 macrophage [J].
Li, Jiangbing ;
Xue, Hao ;
Li, Tingting ;
Chu, Xili ;
Xin, Danqing ;
Xiong, Ye ;
Qiu, Wei ;
Gao, Xiao ;
Qian, Mingyu ;
Xu, Jiangye ;
Wang, Zhen ;
Li, Gang .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2019, 510 (04) :565-572
[92]   Thrombin-activated platelet-derived exosomes regulate endothelial cell expression of ICAM-1 via microRNA-223 during the thrombosis-inflammation response [J].
Li, Jiannan ;
Tan, Ming ;
Xiang, Qinqin ;
Zhou, Zhou ;
Yan, Hongbing .
THROMBOSIS RESEARCH, 2017, 154 :96-105
[93]   New Insights into the Role of Exosomes in the Heart After Myocardial Infarction [J].
Li, Na ;
Rochette, Luc ;
Wu, Yongxin ;
Rosenblatt-Velin, Nathalie .
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2019, 12 (01) :18-27
[94]   Matrix Vesicles as a Therapeutic Target for Vascular Calcification [J].
Li, Tiantian ;
Yu, Hongchi ;
Zhang, Demao ;
Feng, Tang ;
Miao, Michael ;
Li, Jianwei ;
Liu, Xiaoheng .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 10
[95]   Exosomes secreted by mesenchymal stem cells promote endothelial cell angiogenesis by transferring miR-125a [J].
Liang, Xiaolei ;
Zhang, Lina ;
Wang, Shihua ;
Han, Qin ;
Zhao, Robert Chunhua .
JOURNAL OF CELL SCIENCE, 2016, 129 (11) :2182-2189
[96]   Inflammation in Atherosclerosis [J].
Libby, Peter .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (09) :2045-2051
[97]   Inflammation and atherothrombosis - From population biology and bench research to clinical practice [J].
Libby, Peter ;
Ridker, Paul M. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (09) :A33-A46
[98]   Inflammation during the life cycle of the atherosclerotic plaque [J].
Libby, Peter .
CARDIOVASCULAR RESEARCH, 2021, 117 (13) :2525-2536
[99]   Progress and challenges in translating the biology of atherosclerosis [J].
Libby, Peter ;
Ridker, Paul M. ;
Hansson, Goran K. .
NATURE, 2011, 473 (7347) :317-325
[100]   Mechanical response of a calcified plaque model to fluid shear force [J].
Lin, Tiantian C. ;
Yin Tintut ;
Lyman, Althea ;
Mack, Wendy ;
Demer, Linda L. ;
Hsiai, Tzung K. .
ANNALS OF BIOMEDICAL ENGINEERING, 2006, 34 (10) :1535-1541