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  • 1
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background  Inducible protein (IP)-10 belongs to the CXC chemokine subfamily and acts through the CXCR3 receptors that attract T lymphocytes. Keratinocytes are thought to be the main cell source of this chemokine in the skin, but other sources need to be elucidated.Objectives  To determine whether skin fibroblasts, besides keratinocytes, are able to produce IP-10 and the possible involvement of these cells in pathogenesis of atopic dermatitis (AD).Methods  We studied the production pattern of IP-10 in dermal fibroblasts obtained from healthy donors, AD patients and in the HaCaT cell line (normal human keratinocytes) used as control. We stimulated fibroblasts after the sixth and seventh passage with tumour necrosis factor (TNF)-α, interferon (IFN)-γ, interleukin (IL)-4, and by means of reverse transcriptase–polymerase chain reaction and enzyme-linked immunosorbent assay analysis detected the production pattern of IP-10. To determine whether a different pattern of production of IP-10 by fibroblasts corresponds to the level of this chemokine in the plasma of patients with AD, we also checked the plasma IP-10 levels in 33 AD patients and 10 healthy donors.Results  The pattern of chemokine production between dermal fibroblasts and HaCaT cells was different. The main inducer of IP-10 in fibroblasts was TNF-α, whereas IFN-γ was the main inducer of IP-10 in HaCaT cells. We demonstrate that fibroblasts from AD patients have higher IP-10 expression and are more sensitive to TNF-α stimulation compared with healthy controls. Consequently, IP-10 levels in plasma of AD patients were higher than in healthy donors.Conclusions  Skin fibroblasts could be an important source of IP-10. TNF-α is the main inducer of IP-10 by skin fibroblasts, but not IFN-γ or IL-4. The increased level of IP-10 in the plasma of patients with AD could be connected with increased activity of skin fibroblasts.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    British journal of dermatology 147 (2002), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Summary Background Impaired sweating is thought to be a cause of barrier dysfunction in atopic dermatitis (AD). Objectives To examine the sweating function in AD in a quantitative manner. Methods We investigated the sweating response of lesional and non-lesional skin of adult patients with AD by a quantitative sudomotor axon reflex test in which the axon reflex is stimulated by acetylcholine iontophoresis. Sweat volume on the volar aspect of the forearm was measured in 18 adult patients with AD and in 40 non-atopic controls; five patients with Sjögren's syndrome were also studied as disease comparators. We also evaluated the sweating function in four AD patients after topical corticosteroid therapy. Latency time, direct (DIR) sweat volume and axon reflex-mediated indirect (AXR) sweat volume were the variables studied. Results The latency time in AD patients was significantly prolonged and AXR sweat volume significantly reduced compared with those in non-atopic control subjects. The latency time and AXR sweat volume of lesional AD skin were significantly more prolonged and reduced, respectively, than those of non-lesional skin. In contrast, the DIR sweat volume of lesional or non-lesional AD skin induced by direct stimulation with acetylcholine was only slightly reduced when compared with that in non-atopic controls. Latency time and sweat volumes of lesional and non-lesional AD skin improved after topical corticosteroid therapy. Conclusions These results suggest that the impaired sweat response in AD is attributable to an abnormal sudomotor axon reflex, which is reversed by topical corticosteroid administration.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Clinical and experimental nephrology 4 (2000), S. 281-285 
    ISSN: 1437-7799
    Keywords: Key words Expression profile of nephron segment ; Functional genomics ; Bioinformatics ; Laser microdissection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract An expression profile is a list of expressed genes determined by a direct sequencing of thousands of clones randomly selected from nonbiased and unamplified cDNA libraries. The data depict their relative abundance in analyzed tissues or cells. We constructed the expression profiles of mouse proximal tubules and inner medullary collecting ducts. First, approximately 18 cm and 20 cm of mouse proximal tubules and inner medullary collecting duct, respectively, were collected by microdissection methods, and cDNA libraries were prepared. Second, 1000 to 2000 clones were randomly selected and sequenced, confirming that 646 and 1613 types of transcripts existed in each nephron segment respectively. The profiles revealed that the most abundant gene was kidney androgen-regulated gene (Accession number M22810) for proximal tubule and α-B crystallin (Accession number M63170) for inner medullary collecting duct. The computer-based subtraction was performed using the expression profiles of nephron segments with those of other tissues. It illuminated several putative nephron-specific genes. Northern analyses and in situ hybridization demonstrated that abundant genes appearing more than three times in the profile were predominantly expressed in kidney nephron segments. Recently, the possible roles of proximal tubules in the progression of kidney diseases, especially the adverse effects of proteinuria, have been proposed. To evaluate the hypothesis, proximal tubules were collected from a protein-overloaded proteinuria model and analyzed. The disease profile of model mouse proximal tubule constructed by sequencing approximately 3000 clones was compared with those of normal tubules. The results revealed that proteinuria for one week caused dramatic changes of gene expression in proximal tubules. The results were confirmed by laser-based microdissection along with a reverse transcription-polymerase chain reaction method that allowed us to isolate proxi-mal tubules from histological specimens and to quantify mRNA expression. The expression profiles provided useful bioinformatics concerning kidney diseases, hopefully leading to future applications including development of new therapies, better prognosis, and additional information for diagnosis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 363-365 (Apr. 2001), p. 163-166 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 363-365 (Apr. 2001), p. 159-162 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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