ADAMTS proteases in vascular biology
نویسندگان
چکیده
منابع مشابه
The ADAMTS proteases, extracellular matrix, and vascular disease: waking the sleeping giant(s)!
The importance of proteases as mediators of extracellular matrix (ECM) degradation and vascular cell phenotype in the pathogenesis of vascular disease is indisputable. In fact, excellent cases can be made for the matrix metalloproteinases (MMPs) (see review1), the serine proteases (see review2), and the cysteine and aspartic proteases (see review3) being involved in many of the events in vascul...
متن کاملVASCULAR BIOLOGY Endothelial cell ADAMTS-13 and VWF: production, release, and VWF string cleavage
Human umbilical vein endothelial cell (HUVEC)–released ADAMTS-13 (a disintegrin and metalloprotease with thrombospondin repeats) and HUVEC-secreted von Willebrand factor (VWF) strings were investigated under static conditions that allow the accumulation and analysis of ADAMTS-13. The latter was released constitutively from HUVECs and cleaved the secreted and cell-anchored VWF strings progressiv...
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BACKGROUND Ovarian carcinomas, usually associated with sex hormones dysregulation, are the leading cause of gynecological neoplastic death. In normal ovaries, hormones play a central role in regulating cell proliferation, differentiation, and apoptosis. On the other hand, hormonal alterations also play a variety of roles in cancer. Stimulation by sex hormones potentially affects gene expression...
متن کاملRearranging exosites in noncatalytic domains can redirect the substrate specificity of ADAMTS proteases.
ADAMTS proteases typically employ some combination of ancillary C-terminal disintegrin-like, thrombospondin-1, cysteine-rich, and spacer domains to bind substrates and facilitate proteolysis by an N-terminal metalloprotease domain. We constructed chimeric proteases and substrates to examine the role of C-terminal domains of ADAMTS13 and ADAMTS5 in the recognition of their physiological cleavage...
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ژورنال
عنوان ژورنال: Matrix Biology
سال: 2015
ISSN: 0945-053X
DOI: 10.1016/j.matbio.2015.02.004