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Mice expressing a mutant form of fibrinogen that cannot support fibrin formation exhibit compromised antimicrobial
Joni M Prasad1, Oleg V Gorkun2, Harini Raghu1
1Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH;
Abstract:
Fibrin(ogen) is central to hemostasis and thrombosis and also contributes to multiple physiologic and pathologic processes beyond coagulation. However, the precise contribution of soluble fibrinogen vs insoluble fibrin matrices to vascular integrity, tissue repair, inflammation, and disease has been undefined and unapproachable. To establish the means to distinguish fibrinogen- and fibrin-dependent processes in vivo, Fib(AEK) mice were generated that carry normal levels of circulating fibrinogen but lack the capacity for fibrin polymer formation due to a germ-line mutation in the Aα chain thrombin cleavage site. Homozygous Fib(AEK) mice developed to term and exhibited postnatal survival superior to that of fibrinogen-deficient mice. Unlike fibrinogen-deficient mice, platelet-rich plasma from Fib(AEK) mice supported normal platelet aggregation in vitro, highlighting that fibrinogen(AEK) retains the functional capacity to support interactions with platelets. Thrombin failed to release fibrinopeptide-A from fibrinogen(AEK) and failed to induce polymer formation with Fib(AEK) plasma or purified fibrinogen(AEK) in 37°C mixtures regardless of incubation time. Fib(AEK) mice displayed both an absence of fibrin polymer formation following liver injury, as assessed by electron microscopy, and a failure to generate stable occlusive thrombi following FeCl3 injury of carotid arteries. Fib(AEK) mice exhibited a profound impediment in Staphylococcus aureus clearance following intraperitoneal infection similar to fibrinogen-deficient mice, yet Fib(AEK) mice displayed a significant infection dose-dependent survival advantage over fibrinogen-deficient mice following peritonitis challenge. Collectively, these findings establish for the first time that fibrin polymer is the molecular form critical for antimicrobial mechanisms while simultaneously highlighting biologically meaningful contributions and functions of the soluble molecule.
Insights
Researchers developed Fib(AEK) mice to distinguish fibrinogen and fibrin roles. Fibrin polymer is crucial for antimicrobial defense, while soluble fibrinogen supports platelet function and offers survival advantages in infection.
Area of Science:
- Biochemistry
- Hematology
- Immunology
Background:
- Fibrin(ogen) plays a key role in hemostasis and thrombosis.
- The distinct roles of soluble fibrinogen versus insoluble fibrin matrices in physiological and pathological processes remain unclear.
Purpose of the Study:
- To develop a model system to differentiate fibrinogen-dependent and fibrin-dependent processes in vivo.
- To investigate the specific functions of soluble fibrinogen and insoluble fibrin polymers.
Main Methods:
- Generation of Fib(AEK) mice with a mutation preventing fibrin polymer formation but retaining soluble fibrinogen.
- Assessment of platelet aggregation, thrombus formation, and bacterial clearance in Fib(AEK) mice.
- Electron microscopy to evaluate fibrin polymer formation in vivo.
Main Results:
- Fib(AEK) mice formed normal fibrinogen but lacked fibrin polymer formation.
- These mice exhibited normal platelet aggregation but failed to form stable thrombi and showed impaired bacterial clearance.
- Fib(AEK) mice demonstrated improved survival in peritonitis challenges compared to fibrinogen-deficient mice.
Conclusions:
- Fibrin polymer is essential for antimicrobial mechanisms.
- Soluble fibrinogen retains critical functions, including support of platelet interactions and providing a survival advantage during infection.
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