INT14448
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Fibrilar types I, II and III collagen maintain tissue architecture and rigidity16, while type V and XI proteins regulate the diameter of collagen fibrils.1721 | |||||||||||||||
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The stromal cells secrete an extracellular matrix composed mainly of collagen fibrils arranged in orthogonal lamellae, and proteoglycans [8]. | |||||||||||||||
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The inflammatory process is negligible in diseased tendons, where type I collagen is found in minor proportion, diffusely distributed, and grossly surrounded by type III fibrils. | |||||||||||||||
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In conclusion, the data here presented indicate a marked decrease in proteoglycan synthesis and changes in corneal collagen organization 24 h after in vitro LASIK surgery in human cornea.
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The original area of the collagen gels was the area (2 cm2) of a well of a 24 well plate, before release from the sides of the wells. | |||||||||||||||
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The process of collagen cleavage and denaturation of the triple helical molecule exposes certain protein sequences, termed neoepitopes, within the collagen molecule. | |||||||||||||||
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The type II collagen biomarkers indicative of degradation fall into three groups according to the localization of the particular epitope within the collagen molecule: cleavage neoepitopes localized to the collagenase cleavage site; denaturation neoepitopes localized to the triple-helical domain and made accessible to the detection reagents by unwinding of the triple helix; and epitopes localized to the mature ends or telopeptides of the molecule (Table 2). | |||||||||||||||
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Together with AH9, the sandwich ELISA assay has been used to monitor the release of amino- and carboxy-terminal fragments of type II collagen from cartilage explants treated with IL-1alpha (Croucher and Hollander, 1999). | |||||||||||||||
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The type II collagen biomarkers indicative of degradation fall into three groups according to the localization of the particular epitope within the collagen molecule: cleavage neoepitopes localized to the collagenase cleavage site; denaturation neoepitopes localized to the triple-helical domain and made accessible to the detection reagents by unwinding of the triple helix; and epitopes localized to the mature ends or telopeptides of the molecule (Table 2). | |||||||||||||||
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The present protocol was established with primary human hip joint capsule MFs by varying cell numbers, collagen gel volumes and concentrations, time points of detachment, and different concentrations of TGF-? | |||||||||||||||
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Based on the present case and on those previously reported in the literature, STMF is characterized by: 1) exclusive incidence in the male sex; 2) variable immunoreactivity of the neoplastic cells for desmin, probably reflecting an origin from a peculiar subset of myofibroblasts, or, alternatively, a further myoid differentiation; 3) variable abundance of (hyalinized) collagen; 4) presence of amianthoid fibers. | |||||||||||||||
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Osteochondral explants were fixed and decalcified for 4 weeks and subsequently embedded in paraffin, while collagen gel samples were fixed overnight in a phosphate-buffered solution of 4% Para formaldehyde and embedded in paraffin. 5 ? | |||||||||||||||
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This means that these enzymes dissolve basement membranes, an organization of collagen and extracellular matrices, enabling cancer cells to infiltrate and destroy adjacent normal tissues. | |||||||||||||||
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That is, cancer cells releases collagenase and dissove collagen between cells/tissues. | |||||||||||||||
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Depending on the individual gene expression level in each patient, gene expression variances in regulatory pathways may lead to enhanced inflammation [53,54], angiogenesis [71,72], enhanced collagen synthesis and secretion [9], and/or a reduced rate of apoptosis [73], thus potentially contributing to hyperplasia of the SM [74], collagen-dependent fibrosis of the joints [64], and a prolonged life span of activated synovial cells in RA [73,75]. | |||||||||||||||
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With a decrease in soluble collagen secretion, we hypothesized that the expression of individual ECM components known to be disrupted in leiomyomas may also be regulated by ATRA. | |||||||||||||||
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Leiomyomas are characterized by excessive collagen production in the ECM.7,16 We therefore evaluated the effect of ATRA treatment on collagen production in leiomyoma cell cultures by measuring salt soluble collagen secreted into the media after 24 h of ATRA treatment, prior to one cycle of cell division. | |||||||||||||||
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As shown in Fig. 2, leiomyoma cells demonstrated a decrease in collagen secretion with increasing ATRA exposure. | |||||||||||||||
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In this study, we report that bortezomib used alone and in combination with a glucocorticoid as front-line treatment in previously untreated, bisphosphonate-naïve patients stimulates bone formation not only as shown by an increase in bALP but also through the use of a novel bone marker, pro-collagen type I N-terminal propeptide (PINP) that is released as collagen is deposited and becomes insoluble during the formation of the organic bone matrix (34) and may, therefore, be a better marker for ongoing bone formation. | |||||||||||||||
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The epinephrine-collagen cartridge (EPI-COLL) is sensitive to aspirin and can be used for the detection of aspirin resistance [6]. | |||||||||||||||
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General Comments
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