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Histological comparison of morphea and lichen sclerosus et atrophicus.

Although lichen sclerosus et atrophicus at an early stage and morphea can be differentiated clinically and histologically, both diseases at a late stage present diagnostic difficulties. In this study, collagen and acid glycosaminoglycans in the skin of both morphea and lichen sclerosus et atrophicus were examined by polarization microscopy. Picrosirius red and Toluidine blue (pH 5.8) were used as stains. Under polarized light, the picrosirius red-stained collagen fibers appeared green in the papillary and reticular dermis of morphea, except the fibers immediately below the epidermis, which appeared orange yellow. In lichen sclerosus et atrophicus, the collagen fibers appeared green in the reticular dermis at both early and late stage. In the papillary dermis the fibers appeared orange at an early stage and greenish orange at a late stage. Toluidine blue-stained birefringence in morphea diminished in the presence of MgCl2 at 0.2 M, in lichen sclerosus et atrophicus in the presence of MgCl2 at 0.3 M. Histologically, there were some differences in epidermal changes between the two diseases; the epidermis was thick in morphea and thin in lichen sclerosus et atrophicus. This difference seems to relate to that in the fibers beneath the epidermis.

Humans↗

Polarized Raman confocal microscopy of single gallium nitride nanowires.

Polarized Raman spectra and corresponding Raman scattering intensity images of an isolated gallium nitride nanowire with a diameter of 170 nm are presented. The sensitivity of the confocal microscope combined with a high-resolution piezoelectric stage enables analysis of the crystalline phase and crystallographic orientation of an individual nanowire with an excellent spatial and spectral resolution in a short acquisition time.

Journal Article↗

Nucleotide binding and hydrolysis induces a disorder-order transition in the kinesin neck-linker region.

Kinesin translocation is thought to occur by a conformational change in a region of the motor domain called the neck linker. However, most evidence supporting this hypothesis comes from monomeric constructs unable to move processively. To address this issue, we investigated the neck-linker configuration on microtubule-bound monomeric and dimeric kinesin constructs using single-molecule fluorescence polarization microscopy. We found that the neck-linker region (i) is very mobile in the absence of nucleotides and during steady walking, (ii) decreases mobility and aligns along the microtubule axis in the presence of AMPPNP or ADP + AlF4(-), (iii) is mostly ordered in the monomeric constructs in the presence of ADP + AlF4(-), and (iv) is closer to parallel to the microtubule axis in the dimeric constructs. These results support the proposed role of the neck linker and suggest a coordination mechanism between the two motor domains in the dimer.

Binding Sites↗

Three-dimensional polarization control in microscopy.

We propose an approach to optical microscopy that enables full control over the three-dimensional polarization vector at the focal spot of a high-numerical-aperture lens. The input field to the lens is linearly polarized and no polarization optics are needed. This technique utilizes the azimuthal spatial degree of freedom of the input field. We find that only a small set of low-order azimuthal spatial harmonics contributes to the focused field on axis, and a simple transformation exists between the linear vector space of these harmonics and the three-dimensional polarization-vector space. Controlling the relative complex weights of these azimuthal harmonics produces any desired three-dimensional state of polarization.

Algorithms↗

Interaction between O-carboxymethylchitosan and dipalmitoyl-sn-glycero-3-phosphocholine bilayer.

O-carboxylmethylchitosan (OCMCS), a chitosan derivative, has emerged as a strong polymeric biomembrane perturbant. In this study, the interaction between OCMCS and dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was examined with cross-polarization microscopy, differential scanning calorimetry (DSC) and the surface pressure-area isotherms techniques. Cross-polarized light images showed that OCMCS induced the fusion of small DPPC multilamellar vesicles (MLV) to form large lamellar structures. From DSC measurement, the highest degree of fusion was found at the optimum OCMCS concentrations between 0.0625 and 0.2 mg/ml which are orders of magnitude lower than those required for similar reductions with unmodified chitosan as perturbant. At these concentrations, the association of DPPC and OCMCS enhances the fusion of DPPC vesicles. Surface pressure-area isotherms of DPPC monolayer in the presence of OCMCS imply interactions between OCMCS and DPPC in neutral condition. In comparison with chitosan, OCMCS proved to be a more effective membrane perturbant not only in neutral but also in acidic and basic conditions. The physical driving forces for OCMCS-induced perturbation of DPPC bilayer in neutral conditions are mainly hydrogen bonding and hydrophobic interactions. In acidic or basic conditions, the physical driving forces are dominated by the electrostatic interactions. The strong OCMCS-DPPC interaction will potentially increase the effectiveness of OCMCS for gene or drug delivery.

1,2-Dipalmitoylphosphatidylcholine↗

Methoxy-polyethoxy side-chain silastomers as materials controlling drug delivery by diffusion flux.

The density of a diffusion medium and the solubility of the diffusant in this material are predominant parameters which control the diffusion flux. Side-chain silastomers can be structurally modified in such a manner that density and polarity are widely varied and adjustable to distinct conditions. The synthesis of cross-linked methoxy-polyethoxy side-chain polysiloxanes is performed by reaction of alpha, omega-bis-(trimethyl-silyloxy)-poly-(methyl-hydrogen-siloxane), alpha, omega-divinyl-poly-(dimethyl-siloxane), and 4-propenyloxy-(4'-methoxy-polyethoxy)-biphenyl. Silastomer foils were obtained with side-chains having up to 9 ethoxy groups. Various silastomer types were characterized by DSC-measurements, polarization microscopy, uptake of water and salicylic acid (as model drug), and by permeation measurements. The polarity of the polymers depends on their contents of ethoxy groups influencing the uptake of polar substances. Polymers with penta-ethoxy and hepta-ethoxy groups at the side-chains take up water under swelling. The solubility and the distribution coefficients of salicylic acid are linearly correlated to the weight fractions of the methoxy-polyethoxy groups in all silastomer types. The temperature dependence of the distribution coefficients of the penta-ethoxy and hepta-ethoxy polymer types shows deviations from the Arrhenius equation. As the side-chains occupy considerable volumes, the density of the molecular packing within the cross-linked polysiloxane matrices is high. The arrangement of the side-chain domains, therefore, depends on the chain length of the cross-linker; the diffusion coefficients are influenced by this parameter. Evidence for the existence of a lyotropic liquid-crystalline phase was observed for one type of these polymers only. Methoxy-polyethoxy side-chain silastomers as membranes or matrices are suited for controlled drug delivery. Drug liberation rates and swelling by uptake of water can be widely altered by variations of the side-chain structures.

Diffusion↗

Atomic-scale spin-polarized scanning tunneling microscopy applied to Mn3N2(010).

Atomic-scale spin-polarized scanning tunneling microscopy is demonstrated in the case of the unique surface spin structure of Mn3N2(010) at 300 K. We find that the surface spin structure is manifested as a modulation of the normal atomic row height profile. The atomic-scale spin-polarized image is thus shown to contain two components, one the normal, nonpolarized part, and the other the magnetic, spin-polarized part. A method is presented for separating these two spatially correlated components, and the results are compared with simulations based on integrated local spin density of states calculated from first principles.

Journal Article↗

Amyloid deposits in human hip joints. A macroscopic, light and polarization microscopic and electron microscopic study of congophilic substance with green dichroism in hip joints.

The occurrence of amyloid in capsular tissue and cartilage from human hip joints were studied by the macroscopic iodine/sulphuric acid test, by light and polarization microscopy, and finally by electron microscopy. It is concluded that the congophilic substance with green dichroism, which in an earlier light and polarization microscopic study was found in a large percentage of hip joints of elderly persons, is amyloid.

Aged↗

[Anatomical and histological studies on a microdontic wisdom tooth].

The purpose of this study is to investigate features and histological structures of the microdontic wisdom tooth. Materials investigated in this study deal with a very small upper right microdontic wisdom tooth of a male patient aged thirty-six. It was observed with binocular microscopy and under X-ray. Horizontal ground sections of it were prepared and observed with polarizing microscopy, phase microscopy, microradiograph, and scanning electron microscopy. Total length of this specimen was about 1/2 of the average measurement in Japanese upper third molars, breadth of the crown about 1/3, thickness of the crown about 1/4. It had one cusp and one root. It is considered that one cusp was formed by fusing of the mesiolingual cusp and mesiobuccal one because fundamental features of the buccal and lingual surfaces of upper molars were preserved in this specimen. It is thought that dental tubules in this specimen were formed more densely than those in the common wisdom tooth because the space of retreating odontoblasts of this specimen was limited but that enamel rods in this specimen were formed more thickly than those in the common wisdom tooth because the space of retreating ameloblasts of this specimen was wide. It is considered that the degeneration in this specimen came up to not only the dental form, but also the histological structure of the enamel because the surface layer of the enamel of this specimen was composed of the laminal structure.

Adult↗

Two-dimensional vectorial photonic crystals formed in azo-dye-doped liquid crystals.

A 2D, square lattice, vectorial photonic crystal is formed by vectorial holography using an azo-dye-doped liquid-crystal material. Four coherent beams are interfered to generate a highly stable, switchable polarization holography structure. The formation of the vectorial lattice by the liquid-crystal molecular orientation is confirmed by diffraction pattern and polarization microscopy analysis. Simulations of the alignment and diffraction pattern are in good agreement with the experimental results. Polarization sensitive diffraction behavior is also consistent with the Kakichashvili model.

Journal Article↗

Two-dimensionally periodic phases in mixtures of compounds made of rodlike and bent-core molecules.

We report two distinct types of two-dimensionally periodic phases in different concentration regions of a binary system composed of the bent-core (BC) compound 1,3-phenylene bis[4-(3-methylbenzoyloxy)] 4(') - n-dodecylbiphenyl 4(') -carboxylate (BC12) and the rodlike (R) compound 4-n-octyloxy 4(') -cyanobiphenyl (8OCB). BC12 exhibits only the lamellar B2 phase. 8OCB which has a highly polar cyano end group exhibits the smectic-A(d) phase with a lamellar structure of partial bilayers made of antiparallel pairs of the polar molecules. The molecular arrangements in the two-dimensionally periodic phases have been deduced based on optical microscopy, polarized infrared and x-ray diffraction studies. The arrangement in the two-dimensionally periodic phase in lower concentration ranges of BC12 (24 to 35 mol% ) is dictated by the partial bilayer structure formed by the rods. The BC molecules arrange themselves with their arrow axes parallel to the long axes of the R molecules and the structure conforms to the c2mm space group symmetry. In higher concentration ranges of BC12 (35 to 60 mol% ) the structure is dominated by the BC molecules, to form the familiar B1 phase with the p2mg space group symmetry. The R molecules lie at the interfaces of these domains stabilizing the structure.

Journal Article↗

[Optic methods for measurements of muscle fiber birefringence].

An optical method for measuring the birefringence of muscle fibers was developed, which is realized on an automated Linnick interferometer microscope equipped with a laser. It was shown that the method has some advantages over the methods based on measurements of the intensity of light passing through a crossed polarizer, an analyzer, and a fiber (light polarized microscopy). The method involves direct phase measurements of optical path length at the parallel and perpendicular orientations of the polarization plane of probing radiation. The phase image is reconstructed automatically from interferograms with the use of the four-frame phase-shifting algorithm. The phase images of one and the same central part of the fiber at different orientations of the polarization plane represent two-dimensional numerical maps of the optical path length. The subtraction of these images gives a two-dimensional map of the phase shift, which includes information about the birefringence of the fiber. A formula for birefringence measurements was deduced, which has a certain advantage in comparison to that used earlier in that it does not take into account the thickness of a fiber that depends on the measurement point. The birefringence is normalized to a value of the half sum of phases, which are measured separately in the course of the experiment.

Algorithms↗

Effects of ethylenediaminetetraacetic acid-4 sodium solution on the surface of renal calculi and the uroepithelium.

Tetrasodium ethylenediaminetetraacetic acid is one of the most effective agents that dissolve renal calculi, especially calculi containing calcium. To study the dissolving process of calculi in solutions, with or without trypsin, serial thin sections of renal calculi composed of calcium oxalate and/or phosphate were prepared and observed by polarizing microscopy. The effects of the solution on the surface of human renal calculi and rat uroepithelium also were studied by scanning electron microscopy. A remarkable difference in solubility was noted between the crystalline and the amorphous components in struvite calculi. Under the polarizing microscope the dissolving effect of 5 per cent tetrasodium ethylenediaminetetraacetic acid solution on struvite after 30 minutes of incubation was equivalent to the use of saline for 24 hours. The effect of trypsin was not apparent. However, under the scanning electron microscope trypsin accelerated the dissolving effect of the tetrasodium ethylenediaminetetraacetic acid solution in struvite and calcium oxalate calculi. The contradictory findings of the ineffectiveness of trypsin on the thin sections as opposed to the pronounced changes seen on the surface of the calculi could be attributed to the difference in the exposed area. The results suggest that trypsin does not seem to dissolve calculi but mainly facilitates the solution to permeate the calculi. The cellular arrangement of the uroepithelium was preserved in tetrasodium solution and in 0.04 per cent trypsin tetrasodium ethylenediaminetetraacetic acid solution.

Animals↗

Chromium-induced lymph node histiocytic proliferation after hip replacement. A case report.

BACKGROUND: Prosthetic joint replacement is frequently used for the treatment of degenerative joint disease, rheumatoid arthritis, bone tumors and traumatic lesions. The prostheses contain such materials as titanium, cobalt and chromium. We describe a patient who, after total hip arthroplasty, developed an inguinal-pelvic mass. Fine needle aspiration revealed metallic particles, also seen on light microscopy in reactive pelvic lymph nodes. Ultrastructure was consistent with the presence of foreign particles, while energy dispersive x-ray microanalysis established the presence of chromium. To our knowledge, this is the first report of chromium-related lymph node metallosis diagnosed by fine needle aspiration. CASE: Eight years after total hip arthroplasty, a 78-year-old woman developed a right pelvic cystic mass. Aspiration drainage was performed. Smears from fine needle aspiration showed numerous macrophages with abundant, foamy cytoplasm and round nuclei without atypia. Small, birefringent particles were seen in the cytoplasm. Histopathology showed fibroconnective tissue with chronic inflammation and marked lymph node sinus histiocytosis. Within histiocytes, numerous particles were present, identical to those seen in the smears. Their nature as "foreign bodies" was confirmed by electron microscopy, and the presence of chromium was shown by energy dispersive x-ray analysis. CONCLUSION: Fine needle aspiration and polarized microscopy are excellent techniques to evaluate foreign materials in lymph nodes draining the sites of joint prostheses, thus precluding confusion with other conditions, such as metastatic carcinoma.

Aged↗

[Study of structural changes of contractile muscle proteins with the aid of polarization ultraviolet fluorescence microscopy. 1. Conformational changes of F-actin in the muscle fiber caused by ATP and its analogs].

Increase of anisotropy of F-actin fluorescence of balanus and rabbit muscle fibers under the influence of ATP, AMP and pyrophosphate in EGTA presence was detected by means of the polarized ultraviolet (UV) fluorescent microscopy methods. The fluorescence anisotropy changes are assumed to be associated with the conformational changes in the actin. ATP cause more noticeable changes of actin structure, than pyrophosphate and AMP. The conformational changes in the actin of balanus and rabbit muscle fibres were similar. ATP and its analogs induced also decrease of UV fluorescence anisotropy of A-band which appears to be associated with conformational changes in myosin. It was siggested that the changes in fluorescence of anisotropy of A-bands are due to structural changes in both HMM and LMM parts of myosin molecule.

Actins↗

The first polar body does not predict accurately the location of the metaphase II meiotic spindle in mammalian oocytes.

OBJECTIVE: To evaluate how well polar body location predicts spindle localization and to examine spindle morphology. DESIGN: Randomized, controlled animal study. SETTING: University-affiliated research laboratory. ANIMAL(S): Mature, female golden hamsters. INTERVENTION(S): After superovulation with pregnant mare serum gonadotropin and hCG, metaphase II oocytes were obtained and imaged under digital polarization microscopy. MAIN OUTCOME MEASURE(S): Identify the meiotic spindle in living, unfixed hamster oocytes and determine spindle location relative to the polar body. RESULT(S): Spindles were imaged in 30 oocytes and only in 5 of them could the polar body predict the spindle localization. In the remaining oocytes, the spindles presented a random distribution within the cytoplasm. CONCLUSION(S): These data show that the polar body location is not an accurate predictor for meiotic spindle location in mammalian oocytes.

Animals↗

[Changes in the ratio of collagen type I and III in the interlobular interstitium of the lung in sudden infant death--a pilot study].

In a blind study the interlobular interstitial connective tissue in paraffin embedded lung sections from 45 autopsy cases aged under 2 years (23 SIDS and 22 Non-SIDS) were investigated with the aim of determining the collagen type I:type III ratio by means of polarimetric evaluation. Sections were stained with Resorcin-Fuchsin for elastin fibres, Celestine Blue/Mayer's Haematoxylin for nuclear details and with Solophenyl Red 3 BL in saturated picric acid solution for the differential staining of type I and type III collagen fibres for polarization microscopy. The type I fibres were orange and the type III fibres green in colour. The spectral distribution of the coloured polarized light from the sections was determined and peaks were evident at the wavelengths 590 nm for the orange coloured light of type I and 490 nm for the green coloured light of type III collagen. With corresponding filtres the intensities of the orange and green emissions were separately measured at several points adjacent to lymphatic vessels. The ratio collagen I/III, deduced from the ratio of the intensities of orange to green light, was significantly higher in the SIDS-group than in the Non-SIDS-group (a = 0.001) due to the increase in the amount of collagen type I and could indicate an insiduous fibrosis resulting from lymphostasis.

Collagen↗

Microtubules: a brief historical perspective.

Microtubules are cylindrical organelles of varying length, an overall diameter of 25 nm, and a central hollow core of approximately 5 nm thick. They constitute one of three major structural components of the cytoskeleton and are found in almost all eukaryotic cells, where they perform a variety of essential functions, including chromosome movement, vesicular traffic, beating of cilia and flagella, and maintenance of cell form and morphogenesis. Although microtubules were discovered by transmission electron microscopy in the late 1950s, biophysical evidence for their dynamic structure and function in mitosis was obtained almost a decade earlier through polarizing microscopy. Research on the morphology and molecular structure of microtubules spans 3 decades and is now entering an exciting new "biophysical" era, as described in this issue.

Animals↗