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  • 1
    ISSN: 1435-702X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We investigated the origin of fibronectin (FN) on five posterior and four anterior chamber explanted intraocular lenses (IOLs) using immunohistochemical methods. Cellular deposits (assumed to be macrophages) and fibrous or membrane-like proteinaceous deposits on the IOLs showed immunoreactivity to an antibody against cellular FN. These proteinaceous deposits were believed to be products of the cells that adhered to the IOLs.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-702X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  • Background: Bleeding into the subretinal space in the vicinity of the macula is associated with age-related macular degeneration or retinal arterial macroaneurysm. The prognosis for restoration of vision is poor in the presence of blood clots. • Methods: Using a simple device composed of three disposable syringes we injected tissue-type plasminogen activator (tPA) into the subretinal space during conventional vitrectomy in six patients to assist the draining of subretinal clots. • Results: Four of six patients recovered their visual acuity postoperatively, while visual acuity in the other patients was stabilized. • Conclusion: Early drainage of subretinal hemorrhage assisted by the introduction of tPA into the subretinal space led to uncomplicated surgery and favorable postoperative results.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-702X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  · Purpose: We used immunohistochemistry to characterize cellular and proteinaceous deposits on the surfaces of explanted posterior chamber intraocular lenses (PC-IOLs). · Methods: A total of 30 PC-IOLs were immunostained for the α- or β-subunits of prolyl 4-hydroxylase, which is involved in collagen biosynthesis; cellular fibronectin; αB crystalline; and CD68, a macrophage marker, to characterize the cellular deposits that adhere to the IOL surfaces and to evaluate the distribution of cells involved in the deposition of extracellular matrix on IOLs. · Results: Cellular or proteinaceous deposits were observed on all 30 PC-IOLs. Cells that showed positive staining for αB crystallin were classified as lens epithelial cells; CD68-positive cells were considered to be of macrophagic origin. Positivity for cellular fibronectin, including the macrophages and related cells, appeared to be responsible for the accumulation of fibronectin on the surfaces of PC-IOLs. Prolyl 4-hydroxylase-positive cells were involved in the deposition of collagen on PC-IOLs. · Conclusion: Immunohistochemical study revealed that macrophages, foreign-body giant cells, and lens epithelial cells adhered to explanted PC-IOLs. Such adherent cells are responsible for the deposition of extracellular matrix on the surfaces of PC-IOLs and may regulate the assembly of the extracellular matrix, influencing the biocompatibility of PC-IOLs.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Graefe's archive for clinical and experimental ophthalmology 238 (2000), S. 283-294 
    ISSN: 1435-702X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Purpose: To establish the alteration in expression pattern of transforming growth factor (TGF)-βs and their receptors during repair of lens capsules after cataract surgery, we immunohistochemically located TGF-β isoforms and their receptors in human lens capsules before and after cataract surgery.  Methods: Ten post-cataract surgery capsular specimens were obtained during vitrectomy. Three sections of the anterior capsules were obtained during cataract surgery. A whole lens capsular bag immediately after lens extraction was obtained during vitrectomy. Cryosections of these specimens were processed for immunohistochemical analysis for TGF-β1, TGF-β2, TGF-β3, TGF-β receptor type I (TβR-I), type II (TβR-II) and type III (TβR-III), and were observed under light micros-copy. Results: Lens epithelial cells (LECs) lining the inner surface of the anterior capsules exhibited immunoreactivity for TGF-β2 and TβR-II. Immunoreactivity for TGF-β1, -β3, TβR-I and TβR-III was negative. In the whole capsular bag specimen, equatorial LECs were positive for TGF-β1 and -β2, but not for -β3. In post-cataract surgery specimens, antibodies for each TGF-β isoform labelled either the LECs or ECM accumulated on the capsules. Post-surgical LECs expressed TβR-I and TβR-II, and had also TβR-III in seven of the nine specimens examined.  Conclusion: Expression pattern of TGF-β s in quiescent LECs showed regional heterogeneity. Anterior LECs exhibited TGF-β2 immunoreactivity, while equatorial LECs were positive for TGF-β1 and -β2. Quiescent LECs expressed TβR-II. LECs proliferating around IOLs expressed proteins of each TGF-β isoform and each TβR. TGF-β s were also localized in the ECM on capsules undergoing repair. TGF-β3, TβR-I and TβR-III are up-regulated in LECs after cataract surgery.
    Type of Medium: Electronic Resource
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