Nasal Epithesis Retained by Basal (Disk) Implants

2010 ◽  
Vol 21 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Vitomir S. Konstantinović ◽  
Vojkan M. Lazić ◽  
Ihde Stefan
Keyword(s):  
2002 ◽  
Vol 724 ◽  
Author(s):  
María S. Fernández ◽  
Italo Vergara ◽  
Alejandro Oyarzún ◽  
José I. Arias ◽  
Renato Rodríguez ◽  
...  

AbstractAustromegabalanus psittacusis a large (normally up to 30 cm high) sessile balanomorph barnacle from the coast of Chile and South Peru. Its hard shell is composed of twelve calcareous side plates, six parietes and six radii, joined in the form of a truncated cone opened at the top. Plates rest on a basal disk firmly cemented to the substratum. Although the crystalline microstructure of barnacle's shell has been studied to some extent, its organic composition and the mechanisms governing the biomineralization of such highly ordered nanocomposite have remained obscure. By using X-ray diffraction, infrared spectrometry, SEM and TEM electron microscopy, histochemistry, immuno-histochemistry and -ultrastructure, biochemistry and a crystallization assay, we have studied the cell-shell interactions, the crystalline microstructure of the inorganic moiety and the localization of particular macromolecules, and tested their influence on crystallization.The mineral of the plates and basal disk was calcite showing a (104) preferential orientation. Plates were not solid but porous. While parietes have longitudinal canals (from the base to the apex), radii have transversal canals arranged parallel to the base. These canals are not in the center of the plates but displaced to the outside of the shell delimiting a thinner solid outer lamina and a thicker inner one. The inner lamina consisted of parallel calcified layers separated by organic sheets. These sheets showed autofluorescence and consisted of chitin surrounded by proteoglycans and other minor proteins, which seems to be responsible for the fluorescent behaviour. These organic sheets were also organized as several concentric rings around the canals. The shell matrix obtained after decalcification, which surrounded the crystals, also contained a loose net of such proteoglycans. Mantle epithelial cells covered the entire surface of the inner side of the inner lamina and extend to the plate canals. While isolated chitin did not promote or alter calcite crystallization, the proteoglycan-rich fraction dramatically modified crystal morphology and size. As we have demonstrated in another model of biomineralization, such as the eggshell, hereby we suggest that these structured polyanionic proteoglycan moieties could also be part of the regulatory mechanisms of the barnacle shell mineralization.


1973 ◽  
Vol 19 (3) ◽  
pp. 309-313 ◽  
Author(s):  
Judith F. M. Hoeniger ◽  
H.-D. Tauschel ◽  
J. L. Stokes

Sphaerotilus natans developed sheathed filaments in stationary liquid cultures and motile swarm cells in shaken ones. Electron microscopy of negatively stained preparations and thin sections showed that the sheath consists of fibrils. When the filaments were grown in broth with glucose added, the sheath was much thicker and the cells were packed with granules of poly-β-hydroxybutyrate.Swarm cells possess a subpolar tuft of 10 to 30 flagella and a polar organelle which is usually inserted in a lateral position and believed to be ribbon-shaped. The polar organelle consists of an inner layer joined by spokes to an accentuated plasma membrane. The flagellar hook terminates in a basal disk, consisting of two rings, which is connected by a central rod to a second basal disk.


Science ◽  
1968 ◽  
Vol 159 (3820) ◽  
pp. 1246-1247 ◽  
Author(s):  
H. K. MacWilliams ◽  
F. C. Kafatos
Keyword(s):  

1966 ◽  
Vol 14 (1-2) ◽  
pp. 74-84 ◽  
Author(s):  
Delbert E. Philpott ◽  
Alfred B. Chaet ◽  
Allison L. Burnett

2012 ◽  
Vol 38 (5) ◽  
pp. 611-616 ◽  
Author(s):  
Guillaume Odin ◽  
Carl E Misch ◽  
Itzak Binderman ◽  
Gerard Scortecci

Rehabilitation of severely atrophic jaws is facilitated when basal disk implants are used after activation of the future bony implant bed with a purpose-designed instrument (Osteotensor) 45 to 90 days before implant surgery. Fabrication of a highly rigid, screw-secured fixed prosthesis that acts as an external orthopedic fixator permits immediate functional loading. This protocol also represents a second chance for patients who have experienced complete implant loss and/or bone graft failure.


Development ◽  
2000 ◽  
Vol 127 (4) ◽  
pp. 907-920 ◽  
Author(s):  
A.A. Leontovich ◽  
J. Zhang ◽  
K. Shimokawa ◽  
H. Nagase ◽  
M.P. Sarras

As a member of Cnidaria, the body wall of hydra is structurally reduced to an epithelial bilayer with an intervening extracellular matrix (ECM). Biochemical and cloning studies have shown that the molecular composition of hydra ECM is similar to that seen in vertebrates and functional studies have demonstrated that cell-ECM interactions are important to developmental processes in hydra. Because vertebrate matrix metalloproteinases (MMPs) have been shown to have an important role in cell-ECM interactions, the current study was designed to determine whether hydra has homologues of these proteinases and, if so, what function these enzymes have in morphogenesis and cell differentiation in this simple metazoan. Utilizing a PCR approach, a single hydra matrix metalloproteinase, named HMMP was identified and cloned. The structure of HMMP was similar to that of vertebrate MMPs with an overall identity of about 35%. Detailed structural analysis indicated some unique features in (1) the cysteine-switch region of the prodomain, (2) the hinge region preceding the hemopexin domain, and (3) the hemopexin domain. Using a bacterial system, HMMP protein was expressed and folded to obtain an active enzyme. Substrate analysis studies indicated that recombinant HMMP could digest a number of hydra ECM components such as hydra laminin. Using a fluorogenic MMP substrate assay, it was determined that HMMP was inhibited by peptidyl hydroxamate MMP inhibitors, GM6001 and matlistatin, and by human recombinant TIMP-1. Whole-mount in situ studies indicated that HMMP mRNA was expressed in the endoderm along the entire longitudinal axis of hydra, but at relatively high levels at regions where cell-transdifferentiation occurred (apical and basal poles). Functional studies using GM6001 and TIMP-1 indicated that these MMP inhibitors could reversibly block foot regeneration. Blockage of foot regeneration was also observed using antisense thio-oligo nucleotides to HMMP introduced into the endoderm of the basal pole using a localized electroporation technique. Studies with adult intact hydra found that GM6001 could also cause the reversible de-differentiation or inhibition of transdifferentiation of basal disk cells of the foot process. Basal disk cells are adjacent to those endoderm cells of the foot process that express high levels of HMMP mRNA. In summary, these studies indicate that hydra has at least one MMP that is functionally tied to morphogenesis and cell transdifferentiation in this simple metazoan.


2006 ◽  
Vol 123 (5) ◽  
pp. 352-361 ◽  
Author(s):  
Yasuko Amimoto ◽  
Rie Kodama ◽  
Yoshitaka Kobayakawa
Keyword(s):  

1970 ◽  
Vol 23 (3) ◽  
pp. 380-398 ◽  
Author(s):  
H.K. MacWilliams ◽  
F.C. Kafatos ◽  
W.H. Bossert

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