176 research outputs found
Membrane lipid interactions in intestinal ischemia/reperfusion-induced Injury
Ischemia, lack of blood flow, and reperfusion, return of blood flow, is a common phenomenon affecting millions of Americans each year. Roughly 30,000 Americans per year experience intestinal ischemia-reperfusion (IR), which is associated with a high mortality rate. Previous studies of the intestine established a role for neutrophils, eicosanoids, the complement system and naturally occurring antibodies in IR-induced pathology. Furthermore, data indicate involvement of a lipid or lipid-like moiety in mediating IR-induced damage. It has been proposed that exposure of neo-antigens are recognized by antibodies, triggering action of the complement cascade. While it is evident that the pathophysiology of IR-induced injury is complex and multi-factorial, we focus this review on the involvement of eicosanoids, phospholipids and neo-antigens in the early pathogenesis. Lipid changes occurring in response to IR, neo-antigens exposed and the role of a phospholipid transporter, phospholipid scramblase 1 will be discussed
Struktuur van de amino-terminus van het A-eiwitgen en van een polynukleotidefragment uit het replikase-gebied van de R.N.A. bakteriofaag MS2 / Joseph Merregaert.
Characterization of the stromal osteogenic cell line MN7 : mRNA steady-state level of selected osteogenic markers depends on cell density and is influenced by 17<tex>\beta$</tex>-estradiol
The extracellular matrix protein 1 (ECM1) in skin biology : an update for the pleiotropic action
Extracellular matrix protein 1 (ECM1) is a secreted glycoprotein that plays a pivotal role in the structural and
homeostatic biology of the skin, particularly in angiogenesis, reconstitution of basement membrane, proliferation and
differentiation of epidermal keratinocytes and dermal fibroblasts, and malignant transformation. This rationale is
substantiated by loss-of-function mutations in the ECM1 gene in an autosomal recessive genodermatosis lipoid
proteinosis and circulating IgG autoantibodies to this molecule in a humoral autoimmune condition lichen sclerosus, both
of which are counterpart disease conditions sharing comparable skin pathology. In the recent decade, considerable
progress has been made in determining the in vivo function of ECM1 in animal model studies. Furthermore, underlying
insights arose for the genetic predisposition in inflammatory bowel disease ulcerative colitis, acquisition of immune
tolerance and allergic responses via particular T cell subsets such as CD4+CD25+ regulatory T cells and Th2 cells,
regeneration of certain organs, and clinical advantages for diagnostic and prognostic significance in various cancers.
Following our latest review in 2009, we now update the most recent evidences for the pleiotropic action of ECM1 in skin
research, and also highlight the novel pathogenic relevance of this molecule in a variety of human disorders.</jats:p
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