Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 23, Issue 13, Pages -Publisher
MDPI
DOI: 10.3390/ijms23137336
Keywords
chronic immune inflammation; systemic lupus erythematosus; platelets; clot contraction; hemostatic disorders
Funding
- National Institutes of Health [RO1-HL148227, P01-HL40387, RO1-HL148014]
- Russian Foundation for Basic Research [20-015-00257]
Ask authors/readers for more resources
Platelet dysfunction is a potential mechanism that contributes to hemostatic disorders in autoimmune diseases such as SLE. The activation and altered functionality of platelets in SLE patients, characterized by increased expression of phosphatidylserine and P-selectin, and impaired clot contraction, may lead to both thrombotic and hemorrhagic complications. This understudied pathogenic mechanism highlights the importance of further research in understanding platelet activation and dysfunction in autoimmune diseases.
Autoimmune diseases, including systemic lupus erythematosus (SLE), have a high risk of thrombotic and hemorrhagic complications associated with altered platelet functionality. We studied platelets from the blood of SLE patients and their reactivity. The surface expression of phosphatidylserine, P-selectin, and active integrin alpha IIb beta 3 were measured using flow cytometry before and after platelet stimulation. Soluble P-selectin was measured in plasma. The kinetics of platelet-driven clot contraction was studied, as well as scanning and transmission electron microscopy of unstimulated platelets. Elevated levels of membrane-associated phosphatidylserine and platelet-attached and soluble P-selectin correlated directly with the titers of IgG, anti-dsDNA-antibodies, and circulating immune complexes. Morphologically, platelets in SLE lost their resting discoid shape, formed membrane protrusions and aggregates, and had a rough plasma membrane. The signs of platelet activation were associated paradoxically with reduced reactivity to a physiological stimulus and impaired contractility that revealed platelet exhaustion and refractoriness. Platelet activation has multiple pro-coagulant effects, and the inability to fully contract (retract) blood clots can be either a hemorrhagic or pro-thrombotic mechanism related to altered clot permeability, sensitivity of clots to fibrinolysis, obstructiveness, and embologenicity. Therefore, chronic immune platelet activation followed by secondary platelet dysfunction comprise an understudied pathogenic mechanism that supports hemostatic disorders in autoimmune diseases, such as SLE.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available