p 144: sunflower mannose binding lectin-associated serine protease inhibitor-1 (sfmi-1) and -2: significant inhibitors of mannose binding lectin pathway which helps in multiple sclerosis treatment
نویسندگان
چکیده
one of the important parts of innate immunity is complement system that occurs in three different ways; the classic, the alternative and the lectin pathway. the four pattern recognition molecules that have been identified till now are mannose binding lectin (mbl), a component of lectin pathway, and three ficolins (ficolin1,-2 and -3) which compound to the carbohydrates of the cell surface. mbl associated serine protease1 (masp-1), masp-2 and -3 are three proteases which associate with recognition molecules. also mbl-associated protein 19 and mbl-associated protein 44 are two non-catalytic molecules that their role is association with recognition molecules. masp-1 and masp-2 activate the lectin pathway but function of masp-3 is unclear. although some researches show that masp-3 down regulates activation of two other masps and has a similar role like mbl-association 19 and mbl-association 44 that they inhibit mbl pathway too. researches show that mbl pathway has a critical role in pathogenesis of autoimmune diseases such as multiple sclerosis (ms). researches indicate that levels of mbl pathway activator components (masp-1 and masp-2) are higher in serum plasma of ms patients. inhibiting activators of mbl pathway seems to be useful for ms treatment and reducing its disabilities. sunflower masp inhibitor-1 (sfmi-1) and sunflower masp inhibitor-2 (sfmi-2) are two peptides with 14 amino acids that inhibit masp-1 and masp-2 and block the lectin pathway activation. this article suggests using sfmi-1 and sfmi-2 in drugs to targeted therapy of ms and decreasing its symptoms.
منابع مشابه
P 144: Sunflower Mannose binding Lectin-Associated Serine Protease Inhibitor-1 (SFMI-1) and -2: Significant Inhibitors of Mannose binding Lectin Pathway which Helps in Multiple Sclerosis Treatment
One of the important parts of innate immunity is complement system that occurs in three different ways; the classic, the alternative and the lectin pathway. The four pattern recognition molecules that have been identified till now are Mannose binding lectin (MBL), a component of lectin pathway, and three ficolins (ficolin1,-2 and -3) which compound to the carbohydrates of the cell surface. MBL ...
متن کاملMannose-binding lectin (MBL)-associated serine protease (MASP)-1 contributes to activation of the lectin complement pathway.
The complement system plays an important role in innate immunity. In the lectin complement pathway, mannose-binding lectin (MBL) and ficolins act as recognition molecules, and MBL-associated serine protease (MASP) is a key enzyme. It has been suggested that MASP-2 is responsible for the activation of C4. Other serine proteases (MASP-1 and MASP-3) are also associated with MBL or ficolins; howeve...
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multiple sclerosis (ms) is a complex, demyelinating disease of the central nervous system (cns) with variable phenotypic presentations, while guillain-barre syndrome (gbs) is the prototypic acute inflammatory disorder that affects the peripheral nervous system. myasthenia gravis (mg) is a t cell dependent and antibody mediated autoimmune disease. although it has been shown that complement plays...
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Few reports have described in detail a true autoactivation process, where no extrinsic cleavage factors are required to initiate the autoactivation of a zymogen. Herein, we provide structural and mechanistic insight into the autoactivation of a multidomain serine protease: mannose-binding lectin-associated serine protease-2 (MASP-2), the first enzymatic component in the lectin pathway of comple...
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The complement system, an essential part of the innate immune system, can be activated through three distinct routes: the classical, the alternative, and the lectin pathways. The contribution of individual activation pathways to different biological processes can be assessed by using pathway-selective inhibitors. In this paper, we report lectin pathway-specific short peptide inhibitors develope...
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عنوان ژورنال:
مجله علوم اعصاب شفای خاتمجلد ۵، شماره ۲، صفحات ۱۷۵-۱۷۵
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