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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 251 (1974), S. 65-67 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 a, Phase contrast photomicrograph of isolated bovine retinal vessel aggregate. Red blood cells are visible within vessel lumina. x 158. b, Photomicrograph of epoxy-embedded isolated bovine retinal vessel aggregate. Vessels are cut in various planes of section. Non-yascular surrounding ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Fertile hens eggs were incubated 48 hours. Embryos were removed from the shell and the cervical region from each excised and placed in a balanced salt solution containing 1% trypsin for 40 minutes. Notochords were isolated by microdissection and further incubated in vitro 48 or 72 hours. Following trypsinization, unincubated notochords were rod-shaped and were shown by electron microscopy to be devoid of extracellular materials or contaminating mesenchymal cells. Extracellular materials, ultrastructurally indistinguishable from those in the perinotochordal connective tissue space in vivo, are present on the surfaces of cell clusters at 48 hours of in vitro incubation. Areas of fibrillogenesis, in which microfibrils are separated from the surface of cells by intermittent basement lamina, are common. At 72 hours of in vitro incubation fibrogenic activity is less evident, but occasionally intense concentrations of small and large microfibrils, basement lamina and other extracellular substances are seen adjacent to notochordal cell surfaces. These observations are of special interest in light of the known role of the notochord in embryonic induction and recent demonstrations that surface-associated substances (specifically collagen) are necessary for normal cytodifferentiation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 197 (1980), S. 257-276 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The perinotochordal sheath (PNS) is a “tube” of extracellular matrix (ECM) that surrounds the avian notochord beginning in the second day of development. Somites, like the notochord, derive from chordamesoblast but are encased by a less substantial perisomitic matrix (PSM). Initially both tissue types exhibit epithelioid characteristics. Somitic cells subsequently disperse, however, while notochordal histoarchitecture is maintained until much later. To test the possible shape-preserving role of the PNS, notochords were isolated from chick embryos by homogenization (which retains the sheath) or by trypsinization (which removes the sheath). Somites were similarly isolated. Tissues were cultured 12-72 hours and studied by LM, SEM and TEM. Mechanically isolated notochords are initially rigid with smooth surfaces. During the culture period a few cells grow outward from cut ends of the notochord, but its overall rod shape and intact PNS are maintained. In contrast, uncultured trypsinized notochords are flaccid, denuded cylinders with numerous cytoplasmic blebs. They adhere to the substratum within 12 hours of culture when a few cells break away from the central tissue rod, migrate laterally, and appear mesenchymal. This cellular dispersion is directional (perpendicular to the long notochordal axis) and continuous (up to 72 hours). At this time a flattened ovoid growth area is formed. Cultured somites form flat circular growth areas within 12 hours of culture irrespective of the isolation method. These data suggest that the maintenance of an epithelial configuration by notochords in vivo may be due in part to physical restraints of the PNS. It seems possible that notochordal secretions (manifested by the formation of a PNS) could result in its compartmentation and axial confinement while its unrestrained somitic relatives are free to disperse.
    Additional Material: 29 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 226 (1990), S. 295-306 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Human retinas from persons with diabetic retinopathy and agematched controls were rendered acellular by sequential detergent treatment. The resulting network of microvascular extracellular matrix (ECM) materials, including basement membranes (BMs), was compared by TEM and, following cryofracture, by SEM. Our study demonstrates that in diabetics, retinal capillary BM complexes are generally thickened and that their ECM subcomponents, including BM leaflets and BM-like pericytic matrix (PCM), are differentially altered. Two diabetic microvessel types were identified. In type A vessels, ECM expansion is manifested by loosely arranged combinations of concentric PCM layers and collagen fibrils with thickened subendothelial (EBM) and pericyte (PBM) BM leaflets. Type B vessels show densely compact central PCM masses and poorly recognizable EBMs and PBMs. In both types, Müller cell BMs (MBMs) are relatively unaffected. High-resolution SEM shows tissue-specific features in normal EBM and MBM surfaces, but disease-related topographic changes are not evident. It is possible that the ECM arrangements identified in our study relate to different microvessel domains and that their specific morphological features may play important roles in the pathogenesis of diabetic retinopathy including capillary closure and neovascularization.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 216 (1986), S. 349-358 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Previous transmission electron microscopic studies have demonstrated glomerular basement membrane (GBM) thickening and mesangial matrix (MM) expansion in chronic stages of diabetes. It is difficult, however, to achieve an appreciation of GBM surface features and distribution of MM in planar views. In the current study, autopsy human renal cortical tissue from patients with end-stage diabetic nephropathy were minced and rendered acellular with detergents prior to fixation, cryofracture, and preparation for light microscopic (LM), transmission electron microscopic (TEM), and scanning electron microscopic (SEM) observation in an effort to visualize extracellular materials in three dimensions.Our studies demonstrated that although diabetic glomerular changes vary widely within and between individuals, most showed alterations primarily affecting peripheral (epithelial) GBM (with MM increased but diffusely distributed), or they exhibited similar GBM changes but with variable nodular MM expansion leading ultimately to capillary occlusion. Both types showed peripheral GBM thickening and demonstrated external surface irregularities that by SEM appeared as “cauliflower-like” lobulations. In these glomeruli, GBM lamellation or reduplication was common with internal layers frequently thrown into lumenward projections.Glomeruli with diffusely distributed MM generally showed patent capillary channels with little evidence of occlusion. By TEM, highly compact, epithelial GBMs were clearly distinguishable from the electron-lucent MM. In these preparations the matrix was concentrated in relatively small discrete masses sometimes covered by a finely fibrillar material, which extended intermittently onto lumenal surfaces of epithelial GBMs.In more advanced stages of MM involvement, glomeruli typically exhibited smooth-surfaced nodules that were increased at the expense of capillary surface area. By TEM, MM nodules were comprised of a meshwork of very fine (20-Å) fibrils surrounding a variety of detergent-resistant structures including collagenous fibrils and non-collagenous 30-nm circular fibrils with 16-nm subunits. By SEM, GBM and MM nodules were not distinguishable and merged to form substantial barriers to capillary blood flow. In those capillary channels remaining patent, inwardly projecting folds and ridges were common GBM features, and frequently thin fenestrated layers, distinctly separate from epithelial GBMs, formed sieve-like linings for the channels. These three-dimensional observations provide unique views of the processes leading to diabetic glomerular occlusion and suggest a potential for this technique in the study of renal BM disease.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 231 (1991), S. 35-47 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Renal glomerular basement membranes (GBMs) exhibit a charge-selective barrier, consisting of heparan sulfate proteoglycan (HSPG) that restricts the passage of anionic molecules into the urine. Previous efforts to localize the HSPG core protein within various layers of the GBM have been contradictory. Furthermore, attempts to correlate proteinuria in several disease states with a decrease in anionic sites of HSPG core protein have yielded conflicting results.When antibodies to HSPG from the EHS tumor matrix [anti-(EHS) HSPG] and GBMs [anti-(GBM) HSPG] were used together with immunogold to label renal tissues from puromycin aminonucleoside nephrotic (PAN) rats, immunolabeling results indicated that a portion of the protein core recognized by anti-(EHS) HSPG was significantly reduced, while immunolabeling with anti-(GBM) HSPG was only slightly reduced in early PAN. Anionic sites (stained with the cationic probe, polyethyleneimine) within the lamina rara externa of the GBM remained unaltered throughout the course of PAN.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 230 (1991), S. 325-331 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Previous attempts to prepare skeletal muscle basal laminae (BL) for ultrastructural analyses have been hampered by difficulties in successfully removing skeletal muscle proteins and cellular debris from BL tubes. In the present study we describe a two phase method which results in an acellular muscle preparation, the BL of which are examined by light, transmission electron, and scanning electron microscopy. In the first phase, excised rat extensor digitorum longus muscles are subjected to x-radiation and then soaked in Marcaine to inhibit muscle regeneration and to destroy peripheral muscle fibers. The muscles are then grafted back into their original sites and allowed to remain in place 7-14 days to allow for maximal removal of degenerating muscle tissue with minimal scar tissue formation. In the second phase, the muscle grafts are subjected sequentially to EDTA, triton X-100, DNAase, and sodium deoxycholate to remove phagocytizing cells and associated degenerating muscle tissue. These procedures result in translucent, acellular muscle grafts which show numerous empty tubes of BL backed by endomysial collagenous fibers. These preparations should be useful for morphological analyses of isolated muscle BL and for possible in vitro studies by which the biological activity of muscle BL can be examined.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Notochords were isolated from Hamburger-Hamilton stages 13-15 chick embryos by trypsinization and microdissection. These were shown by electron microscopy to be completely devoid of extracellular materials or mesenchymal contaminants. Cultivation of notochordal isolates was carried out on a non-collagenous (Falcon Plastic) substratum for 0 to 48 hours. At 12 hours of in vitro incubation, a discontinuous basal lamina could be demonstrated on the surface of notochordal cells. This was followed by the appearance of microfibrils of various sizes and other components of the extracellular matrix. By 48 hours of in vitro incubation, the same extracellular materials which surround the notochord in vivo (notochord sheath) could be demonstated in vitro.Autoradiographic studies show that tritiated proline is taken up by notochordal cells and secreted to the extracellular space where label is associated with basal lamina, microfibrils and ground substance. When cis-hydroxyproline, a known collagen-specific inhibitor is added to the system, tritiated proline label is located primarily intracellularly and fewer areas of active fibrillogenesis are noted. This suggests that ultrastructurally recognizable materials produced by notochordal cells in vitro may be at least partially collagenous. Significantly, these materials are produced in vivo at the same time (following stage 10) that notochordal tissues actively induce somite differentiation and cartilage formation. It seems reasonable that a biochemically or ultrastructurally identifiable component of the extracellular matrix may possibly mediate such induction.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 200 (1981), S. 421-436 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Glomeruli and tubules were isolated from rabbit kidney cortex by mild homogenization and sieving. Mixtures of these renal components were treated with detergents to prepare pellets of morphologically intact and easily distinguishable tubular (TBM) and glomerular basement membranes (GBM). These BMs were prepared for electron microscopy after: (1) no treatment; (2) treatment with buffer alone; or (3) treatment with enzyme (pronase, trypsin, pepsin, collagenase or testicular hyaluronidase). Mixtures of TBMs and GBMs were treated in the same incubation medium to keep constant the enzyme concentration, temperature, pH, and duration of the treatment. Untreated TBMs showed collapsed, highly folded sheets of electron-dense material. In contrast, control GBMs were thinner and strikingly resistant to changes in in vivo histoarchitecture. In all enzymatic treatments except hyaluronidase, TBM was more susceptible to digestion than GBM. In general, the effect of pepsin was greater than trypsin, which was greater than pronase. Collagenase also solubilized TBM but was only slightly effective in attacking GBM. Hyaluronidase-treated BMs were indistinguishable from controls. TBMs and GBMs were both affected least by the enzyme on their epithelial surfaces, which generally remained crisp and sharply demarcated. In contrast, fibrillar materials and BM fragments were released from connective tissue surfaces of TBMs and endothelial-mesangial surfaces of GBMs. Data in the present study indicate that various BMs are morphologically heterogeneous and that a “non-unitary” concept of BM is most appropriate. Moreover, the BM “sidedness” demonstrated following enzymatic digestions strongly suggests that macromolecular complexes within laminae densae may be arranged such a manner that opposing surfaces of the same BM are compositionally disparate.
    Additional Material: 26 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Microscopy Research and Technique 28 (1994), S. 165-177 
    ISSN: 1059-910X
    Keywords: Diabetic nephropathy ; Diabetic retinopathy ; Mesangial matrix ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Basement membranes (BMs) were first described in the mid-19th century, but they were not isolated and prepared for compositional studies until nearly 100 years later. Early methods of isolation were carried out on renal glomeruli, which were first sub-fractionated from kidney tissues by sieving. BMs were then isolated from the glomeruli by ultrasonic disruption, which, following low speed centrifugation, yielded “purified” but highly fragmented BM material. In an effort to obviate the mechanical damage to BMs produced by ultrasound, a sequential detergent solubilization technique was introduced that resulted in morphologically intact BMs from a variety of tissue sub-fractions. This was highly advantageous because “acellular” BMs produced by the procedure could be examined critically by light and electron microscopic methods. Subsequently, this procedure has been utilized to demonstrate the substructural heterogeneity of vascular and non-vascular BMs from a wide variety of animal species. The current review describes the results of scanning and transmission electron microscopic studies of acellular BMs prepared from renal glomeruli and from the retinal microvessels of the eye. These BMs are of particular interest to basic scientists and clinicians because they are altered in several disease states, most notably diabetes mellitus. An effort is made to point out the implications of glomerular and retinal vessel BM changes to the pathogenesis of diabetic kidney and retinal vessel BM disease. © 1994 Wiley-Liss, Inc.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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