The platelet-mitochondria nexus in autoimmune and musculoskeletal diseases

被引:0
作者
Michailidou, Despina [1 ,2 ]
Giaglis, Stavros [3 ,4 ]
Dale, George L. [5 ]
机构
[1] Univ Oklahoma, Div Rheumatol, Hlth Sci Ctr, Oklahoma City, OK 73104 USA
[2] Oklahoma City VA Hlth Care Syst, Div Rheumatol, Oklahoma City, OK USA
[3] Univ Hosp Basel, Dept Biomed, Lab Expt Rheumatol, Basel, Switzerland
[4] Univ Hosp Basel, Dept Rheumatol, Basel, Switzerland
[5] Univ Oklahoma, Dept Med, Hlth Sci Ctr, Oklahoma City, OK USA
关键词
Platelets; Mitochondria; Autoimmune diseases; Musculoskeletal diseases; OXIDATIVE STRESS; OXYGEN; MICROPARTICLES; INFLAMMATION; ACTIVATION; ARTHRITIS; CALCIUM; DNA; PROTEINS; AGGREGATION;
D O I
10.1016/j.clim.2024.110350
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Platelets are crucial for thrombosis and hemostasis. Importantly, they contain mitochondria that are responsible for energy generation and therefore vital for platelet survival and activation. Activated platelets can release mitochondria that may be free or encapsulated in platelet extracellular vesicles (EVs). Extruded mitochondria are a well-known source of mitochondrial DNA, and mitochondrial antigens that can be targeted by autoantibodies forming immune complexes (IC). Interaction of IC with the platelet cell surface Fc gamma RIIA receptor results in platelet activation and release of platelet granule components. In this review, we summarize how platelets and mitochondria may contribute to the pathogenesis of different autoimmune and musculoskeletal diseases. Targeting key drivers of mitochondrial extrusion may ultimately lead to urgently needed targeted pharmacological interventions for treating inflammation and thrombotic diathesis, and halting organ damage in some of these rheumatological conditions.
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页数:6
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