scholarly journals Studies on Cartilage: Electron Microscope Observations on Normal Rabbit Ear Cartilage

1958 ◽  
Vol 4 (4) ◽  
pp. 401-406 ◽  
Author(s):  
Huntington Sheldon ◽  
Robert A. Robinson
Keyword(s):  
Electron Microscope ◽  
Three Dimensional ◽  
Elastic Fibers ◽  
Acid Fuchsin ◽  
Cartilage Cell ◽  
Cell Border ◽  
Rabbit Ear ◽  
The Matrix ◽  
Dense Substance ◽  
Ear Cartilage

Normal rabbit ear cartilage studied with the light and electron microscope shows chondrocytes in which large lipide spherules, and an abundance of glycogen, a few small mitochondria, and relatively few elements of the endoplasmic reticulum can be identified. The chondrocytes contain, in addition, a material which stains strongly with acid fuchsin and appears in the electron microscope as a relatively dense felt-work. In electron micrographs, the matrix of normal rabbit ear cartilage consists of two components: a uniformly distributed moderately dense substance which appears as a fine meshwork without any particular pattern extending from cartilage cell border to cartilage cell border; and a three-dimensional anastomotic network of more dense material, which is best described as "felt-like" lying between the cells. The similarity between the felt-like material of the matrix and the elastic fibers described in previous electron microscope observations is discussed.

scholarly journals STUDIES ON CARTILAGE

1960 ◽  
Vol 8 (1) ◽  
pp. 151-163 ◽  
Author(s):  
Huntington Sheldon ◽  
Robert A. Robinson
Keyword(s):  
Amorphous Material ◽  
Surface Membrane ◽  
Electrophoretic Pattern ◽  
Elastic Component ◽  
Elastic Tissue ◽  
Cell Cytoplasm ◽  
Elastic Cartilage ◽  
Rabbit Ear ◽  
The Matrix ◽  
Ear Cartilage

Electron microscope observations on rabbit ear cartilage following the administration of papain show that both the elastic component of the matrix and the amorphous material disappear leaving a matrix which consists of delicate fibrils which are presumed to be collagen. This unmasking of fibrils coincides with the appearance of an abnormal component in the electrophoretic pattern of the rabbit's serum. The chondrocytes show vacuoles in their cytoplasm which appear at the same time that the cells appear crenated in the light microscope. A ruffly appearance of the cell surface membrane coincides with this vacuolization, and vacuoles often appear open and in continuity with the extracellular space. The resurgence of the rabbit ear is accompanied by a reconstitution of both the amorphous material and the elastic component of the matrix. During this period numerous dilated cisternae of the endoplasmic reticulum which contain a moderately dense material are present in the chondrocyte cytoplasm. We have been unable to demonstrate a direct relationship between the elastic component of the matrix and a particular component of the chondrocyte cytoplasm, but it is clear that changes occur in the cartilage cell cytoplasm during both the depletion and reconstitution of the matrix. Previous studies on the effect of papain on elastic tissue are noted and the possible relationships between changes in the cells and matrix of this elastic cartilage are discussed.

Fine Structure of the Elastic Fibers and the Elastin Crystalloids by Means of Tannic Acid Fixation Method

1976 ◽  
Vol 34 ◽  
pp. 318-319
Author(s):  
V. Mizuhira ◽  
Y. Futaesaku ◽  
H. Nakamura
Keyword(s):  
Fine Structure ◽  
Electron Microscope ◽  
Tannic Acid ◽  
Staining Method ◽  
Fixation Method ◽  
Elastic Fibers ◽  
Osmium Tetraoxide ◽  
Ear Cartilage ◽  
Staining Methods

It is well known that the elastic fibers do not stain well with conventional electron fixation and staining methods. However some investigators have tried to demonstrate elastic fibers as a stained structure under the electron microscope. Greenlee et al.(1966) and Ouintarelli et al.(1973) reported a phosphotaungstic acid staining method for elastic fibers; Albert (1970 & 1971) reported his results using a metalic tetraphenylprophine staining method.In the contrast to these staining methods for elastic fibers, Mizuhira et al (1971,'72, ‘75) have succeeded in demonstrating elastic fibers very clearly using an improved fixation method for proteins with glutaraldehyde containing tannic acid, followed by the osmium tetraoxide method.This new fixation method is very simple. Aorta, ear cartilage, intestine or skin are fixed with 2.5 % glutaraldehyde, containing 0.5 % to 4 % tannic acid buffered with veronal acetate or phosphate at pH 6.8 to 7.2 for 1.5 hrs to overnight.

scholarly journals Facile Fabrication of Environmentally-Friendly Hydroxyl-Functionalized Multiwalled Carbon Nanotubes/Soy Oil-Based Polyurethane Nanocomposite Bioplastics with Enhanced Mechanical, Thermal, and Electrical Conductivity Properties

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 763 ◽  
Author(s):  
Xiaogang Luo ◽  
Zengcheng Yu ◽  
Yixin Cai ◽  
Qiangxian Wu ◽  
Jian Zeng
Keyword(s):  
Carbon Nanotubes ◽  
Electrical Conductivity ◽  
Electron Microscope ◽  
Multiwalled Carbon Nanotubes ◽  
Three Dimensional ◽  
Mechanical Analysis ◽  
Multiwalled Carbon ◽  
Methylene Diphenyl Diisocyanate ◽  
The Matrix ◽  
Functionalized Multiwalled Carbon Nanotubes

It is challenging to prepare polyurethane bioplastics from renewable resources in a sustainable world. In this work, polyurethane nanocomposite bioplastics are fabricated by blending up to 80 wt % of soy-based polyol and petrochemical polyol with hydroxyl-functionalized multiwalled carbon nanotubes (MWCNTs-OH). The scanning electron microscope (SEM), transmission electron microscope (TEM), and Fourier transform infrared spectroscopy (FTIR) analyses reveal homogeneous dispersion of the MWCNTs-OH in the matrix, as well as interaction or reaction of MWCNTs-OH with the matrix or polymeric methylene diphenyl diisocyanate (pMDI) in forming the organic–inorganic hybrid bioplastic with a three-dimensional (3D) macromolecule network structure. Mechanical properties and electrical conductivity are remarkably enhanced with the increase of the multiwalled carbon nanotube (MWCNTs) loading. Dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA) results show that the bioplastics with MWCNTs-OH have a better thermal stability compared with the bioplastics without MWCNTs-OH. The composition of the nanocomposites, which defines the characteristics of the material and its thermal and electrical conductivity properties, can be precisely controlled by simply varying the concentration of MWCNTs-OH in the polyol mixture solution.

Electron microscopy and diffraction studies of polyimides

1983 ◽  
Vol 41 ◽  
pp. 28-29
Author(s):  
O.C. de Hodgins ◽  
K. R. Lawless ◽  
R. Anderson
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Structural Features ◽  
Inert Atmosphere ◽  
Polyimide Films ◽  
Resolution Electron ◽  
The Matrix ◽  
High Resolution Electron Microscope ◽  
Diffraction Patterns ◽  
Polymeric Samples

Commercial polyimide films have shown to be homogeneous on a scale of 5 to 200 nm. The observation of Skybond (SKB) 705 and PI5878 was carried out by using a Philips 400, 120 KeV STEM. The objective was to elucidate the structural features of the polymeric samples. The specimens were spun and cured at stepped temperatures in an inert atmosphere and cooled slowly for eight hours. TEM micrographs showed heterogeneities (or nodular structures) generally on a scale of 100 nm for PI5878 and approximately 40 nm for SKB 705, present in large volume fractions of both specimens. See Figures 1 and 2. It is possible that the nodulus observed may be associated with surface effects and the structure of the polymers be regarded as random amorphous arrays. Diffraction patterns of the matrix and the nodular areas showed different amorphous ring patterns in both materials. The specimens were viewed in both bright and dark fields using a high resolution electron microscope which provided magnifications of 100,000X or more on the photographic plates if desired.

Freeze-Fracture Replication in the Ultrastructure of Blue-Green Algae

1967 ◽  
Vol 25 ◽  
pp. 74-75
Author(s):  
L. V. Leak
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Green Algae ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Electron Microscopic ◽  
Photosynthetic Membranes ◽  
Blue Green Algae ◽  
Cell Biol ◽  
Cellular Components

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.

A Scanning Electron Microscope Study of Isolated Guard Cells

1973 ◽  
Vol 31 ◽  
pp. 454-455 ◽  
Author(s):  
P. Dayanandan ◽  
P. B. Kaufman
Keyword(s):  
Electron Microscope ◽  
Electron Microscope Study ◽  
Three Dimensional ◽  
Guard Cells ◽  
Scanning Electron Microscope Study ◽  
Psilotum Nudum ◽  
Subsidiary Cells ◽  
Welwitschia Mirabilis ◽  
Cycas Revoluta ◽  
Scanning Electron

A three dimensional appreciation of the guard cell morphology coupled with ultrastjuctural studies should lead to a better understanding of their still obscure dynamics of movement. We have found the SEM of great value not only in studies of the surface details of stomata but also in resolving the structures and relationships that exist between the guard and subsidiary cells. We now report the isolation and SEM studies of guard cells from nine genera of plants.Guard cells were isolated from the following plants: Psilotum nudum, four species of Equisetum, Cycas revoluta, Ceratozamia sp., Pinus sylvestris, Ephedra cochuma, Welwitschia mirabilis, Euphorbia tirucalli and Allium cepa.

A New 1000kv Electron Microscope

1969 ◽  
Vol 27 ◽  
pp. 100-101
Author(s):  
J.L. Williams ◽  
K. Heathcote ◽  
E.J. Greer
Keyword(s):  
Electron Microscope ◽  
Direct Observation ◽  
High Voltage ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Specimen Thickness ◽  
Voltage Electron ◽  
High Voltage Electron Microscope ◽  
Dynamic Experiments ◽  
Conventional Instrument

High Voltage Electron Microscope already offers exciting experimental possibilities to Biologists and Materials Scientists because the increased specimen thickness allows direct observation of three dimensional structure and dynamic experiments on effectively bulk specimens. This microscope is designed to give maximum accessibility and space in the specimen region for the special stages which are required. At the same time it provides an ease of operation similar to a conventional instrument.

Methods for making stereoslides and -prints, with freeze-etched olfactory epithelium as example

1984 ◽  
Vol 42 ◽  
pp. 704-705
Author(s):  
Bert Ph. M. Menco ◽  
Ido F. Menco ◽  
Frans L.T. Verdonk
Keyword(s):  
Electron Microscope ◽  
Olfactory Epithelium ◽  
Three Dimensional ◽  
Supporting Cell ◽  
Structural Features ◽  
Extensive Study ◽  
Sprague Dawley ◽  
Freezing Method ◽  
Respiratory Epithelia ◽  
Three Dimensional Presentation

Previously we presented an extensive study of the distributions of intramembranous particles of structures in apical surfaces of nasal olfactory and respiratory epithelia of the Sprague-Dawley rat. For the same structures these distributions were compared in samples which were i) chemically fixed and cryo-protected with glycerol before cryo-fixation, after excision, and ii)ultra-rapidly frozen by means of the slam-freezing method. Since a three-dimensional presentation markedly improves visualization of structural features micrographs were presented as stereopairs. Two exposures were made by tiling the sample stage of the electron microscope 6° in either direction with an eucentric goniometer. The negatives (Agfa Pan 25 Professional) were reversed with Kodak Technical Pan Film 2415 developed in D76 1:1. The prints were made from these reversed negatives. As an example tight-junctional features of an olfactory supporting cell in a region where this cell conjoined with two other cells are presented (Fig. 1).

Designing TIMP (tissue inhibitor of metalloproteinases) variants that are selective metalloproteinase inhibitors

2003 ◽  
Vol 70 ◽  
pp. 201-212 ◽  
Author(s):  
Hideaki Nagase ◽  
Keith Brew
Keyword(s):  
Three Dimensional ◽  
Therapeutic Interventions ◽  
Tissue Inhibitors Of Metalloproteinases ◽  
Structural Basis ◽  
Structural Elements ◽  
Ridge Structure ◽  
Extracellular Matrix Components ◽  
Metalloproteinase Inhibitors ◽  
The Matrix ◽  
A Disintegrin And Metalloproteinase

The tissue inhibitors of metalloproteinases (TIMPs) are endogenous inhibitors of the matrix metalloproteinases (MMPs), enzymes that play central roles in the degradation of extracellular matrix components. The balance between MMPs and TIMPs is important in the maintenance of tissues, and its disruption affects tissue homoeostasis. Four related TIMPs (TIMP-1 to TIMP-4) can each form a complex with MMPs in a 1:1 stoichiometry with high affinity, but their inhibitory activities towards different MMPs are not particularly selective. The three-dimensional structures of TIMP-MMP complexes reveal that TIMPs have an extended ridge structure that slots into the active site of MMPs. Mutation of three separate residues in the ridge, at positions 2, 4 and 68 in the amino acid sequence of the N-terminal inhibitory domain of TIMP-1 (N-TIMP-1), separately and in combination has produced N-TIMP-1 variants with higher binding affinity and specificity for individual MMPs. TIMP-3 is unique in that it inhibits not only MMPs, but also several ADAM (a disintegrin and metalloproteinase) and ADAMTS (ADAM with thrombospondin motifs) metalloproteinases. Inhibition of the latter groups of metalloproteinases, as exemplified with ADAMTS-4 (aggrecanase 1), requires additional structural elements in TIMP-3 that have not yet been identified. Knowledge of the structural basis of the inhibitory action of TIMPs will facilitate the design of selective TIMP variants for investigating the biological roles of specific MMPs and for developing therapeutic interventions for MMP-associated diseases.

3D simulation of emulsion flow using the boundary element method on the heterogeneous computational systems

2012 ◽  
Vol 9 (1) ◽  
pp. 142-146
Author(s):  
O.A. Solnyshkina
Keyword(s):  
Boundary Element Method ◽  
Boundary Element ◽  
Three Dimensional ◽  
Reynolds Numbers ◽  
Problem Size ◽  
Low Reynolds Numbers ◽  
Infinite Domains ◽  
The Matrix ◽  
Computational Systems ◽  
Element Method

In this work the 3D dynamics of two immiscible liquids in unbounded domain at low Reynolds numbers is considered. The numerical method is based on the boundary element method, which is very efficient for simulation of the three-dimensional problems in infinite domains. To accelerate calculations and increase the problem size, a heterogeneous approach to parallelization of the computations on the central (CPU) and graphics (GPU) processors is applied. To accelerate the iterative solver (GMRES) and overcome the limitations associated with the size of the memory of the computation system, the software component of the matrix-vector product

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