Scanning electron microscopy最新文献

Alligator lizards were exposed to broadband noise ranging in intensity from 106 to 132 dB SPL for two hours and permitted to recover from 19 to 62 days. Hearing loss was assessed by comparing the auditory nerve component of the cochlear potential recorded at the end of the recovery period with that recorded before the noise exposure. The stereocilia in these ears were examined with a scanning electron microscope. These sensory hairs showed pathological changes similar to those described in mammalian cochleas with noise-induced damage. In decreasing order of severity the damage included completely missing auditory papillas, missing hair cells, missing hairs, hairs fallen over, and hairs that were only moderately splayed apart compared with their normal appearance. Long lasting hearing loss seems to be associated with all of these sensory hair pathologies.

The squamous epithelium lining the rat foregut was removed by incubating fresh, unfixed specimens in 2N sodium bromide. The surface morphology of the exposed subepithelial basal lamina was examined by scanning electron microscopy. Areas examined included hard and soft palates, oropharynx, tongue, esophagus, and forestomach. The basal lamina was continuous were not present at all sites. The saucer-like defects of lymphocyte migration that are present in the basal lamina beneath the squamous epithelium of the skin were not observed in rat foregut. The epithelial-connective tissue interface of the rat esophagus does not have the coiled and branched papillae seen in esophagi of adult humans. The three dimensional shapes of the connective tissue cores of the various lingual papillae are well-demonstrated by this technique and are distinct. The basal lamina of the hard and soft palates are also distinct.

Eggs of Trichuris trichiura were prepared for scanning electron microscopy (SEM) by the dimethylsulfoxide freeze-cracking method. The egg-shell and oocyte were examined by SEM. The egg has a chitinous shell which consists of more than 10 layers of dense lamellae. The shell is bordered by a limiting membrane. An operculum and a collar made of chitinous shell together form the opercular area. The operculum is an empty cavity. The chitinous fibers of the egg-shell in this area are diffuse and loose, with numerous micropores or spaces. The egg-shell in this area therefore appears to form a fine tubular network. The oocyte is an undifferentiated cell with a biconcave drum-like shape. The perivitelline space is conspicuous at both ends of the cell.

The paper deals with methods and results of the microcorrosion cast technique in lymph angiology. For the representation of the special organization of the lymph vascular system including the initial vascular structures, intranodal pathways, bigger collectors, and lymph trunks, the application of various injection techniques is necessary. The interstitial injection of Mercox proves to be suitable to show the initial lymphatics and prelymphatic spaces. Similarly, the intranodal injection makes visible the system of the lymph sinuses and the spaces of the reticular tissue in this organ. Casts of bigger collecting vessels, lymph trunks, and thoracic duct can be obtained by direct injection of the resin into the vascular lumen. Thus, these techniques enable to make visible the structural details of the cast preparations of all parts of the lymphatic system.

The present paper describes a procedure for preparing vascular corrosion casts of rat myocardial microvasculature. Essential components of the procedure include: partial "self clearing" of the heart in vitro; cardiac arrest by infusion of KCl; retrograde aortic root infusion of Mercox-Sevriton casting resin; KOH digestion of ventricular tissue; and desiccation and mounting of casts for scanning electron microscopy. About 50% of rats yielded complete casts. Vasculature closely paralleled muscle fiber orientation. Capillary beds characteristically exhibited branching, many intercapillary cross bridges, and occasional coiling. Average capillary cast diameter (5.6 microns) and intercapillary distance (15 microns) are comparable to results from in vivo studies. From preliminary calculations, vascular volume represents about 10% of the ventricular walls. These data indicate that vascular corrosion casts may be useful in the analysis of pathologic states and in determining the role of potential therapeutic interventions.

Bone marrow aplasia was induced in rats by whole body lethal irradiation (1,000 rads by x-ray), and rats died of irradiation injury within 7 days. Correlative studies at light (LM), transmission (TEM) and scanning electron microscopy (SEM) demonstrated swelling of endothelial and reticular cells and hemorrhage due to detachment of sinus endothelial cells on days 1 and 2. With time, structural recovery occurred without hemopoietic recovery. Reticular cells developed small intracytoplasmic lipid droplets on days 3 and 4. This resulted in fatty aplastic marrow within 7 days. On the other hand, in the marrow of irradiated rats parabiosed with healthy mates by aortic anastomosis, hemopoiesis was initiated by adhesion of nucleated blood cells to fine cytoplasmic pseudopods of fat-stored cells on days 1 and 2 after parabiosis. On days 3 to 5, reticular cells with large lipid droplets and fine pseudopods increased, then hemopoietic foci became clear and extensive. On day 8 after parabiosis, the aplastic bone marrow recovered completely both its structure and hemopoietic activity. Thus, hemopoietic recovery in lethally irradiated marrow begins with recovery of vascular endothelial cells, re-establishment of sinusoidal structure, and morphological and functional recoveries of reticular cells from fat-storage cells by releasing intracytoplasmic lipid droplets. Marrow stromal cells, namely reticular, fat-storage and fibroblastoid cells, share a common cellular origin, and regain their structure and function when fat-storage cells and fibroid cells are placed in contact with hemopoietic precursor cells.

The interface between cells and matrices in mineralized tissues formed in vivo has been studied mainly by looking at the matrix surface, which is easily prepared, and not at the cell surface, which presents problems. Vertebrate calcified tissues range from being acellular to highly cellular, but for all the tissues the formative cells lay down and organise a cell-specific matrix, although this may be deposited initially on a different tissue-type. The formation of hard tissues is a group activity of many cells; resorption is the province of one cell, though it may be controlled by others in the vicinity. Cell-matrix interfaces that develop in vitro have also mainly been studied at the matrix side. The main difficulty with in vitro studies of hard tissue interfaces is that the cells do not have the same activity or even cellular functions as they had in vivo under the complex control of physiological regulation. The question of osteoblastic osteoclasis falls into this category. It is possible to provide new substrata for both formative and resorptive hard tissue cells to test for the interaction between the cells and the 'matrix' on to which they are seeded. The changing cell-matrix interface may also be modelled using computer simulation of osteoclastic movement across a substrate based on known patterns exhibited by other cell types in vitro. Comparison with the shapes of complex resorption pits shows a surprising match. This suggests that the track of the osteoclast due to cell motility and the bone resorptive mechanism resulting in pits along that track are likely to be separately controlled phenomena.

Chromatid activity during the process of nuclear reformation following metaphase is a period of mitosis where little precise information is available. Nuclear reformation requires that chromosomes, at metaphase and chromatids during anaphase and telophase align, position and associate in a clearly defined sequence to insure the specific design of each nucleus. Four cell lines with chromosome numbers ranging from seven to almost seventy were chosen to determine whether the process of nuclear assembly is the same throughout. Chromosomal alignment at metaphase is found to be radial in all four cell lines. Chromosome positioning is essentially the same in all four, where the smaller chromosomes are located centrally and longer ones are positioned peripherally in a radial alignment. Chromosomal association is directly related to chromosome number. The more chromosomes in a one dimensional plane occupying a given area, the closer the association. In comparing the HeLaS3 and muntjac chromatids, the former has the closer association at metaphase. Since association is the most important aspect of chromatid behavior in nuclear reformation, chromatid positioning becomes a vital process during anaphase movement. Chromatid positions established during anaphase determines later positioning in the interphase nucleus because of the subsequent interconnection of adjacent chromatids by the formation of a fibrous meshwork. This fibrous meshwork, formed in anaphase and early telophase, functions to stabilize chromatids following their positioning and it also serves as a substrate or matrix for the assembly of nuclear envelope.

Otolith formation was studied in a mutant strain of low-fertility Delaware chicks which exhibit an otolithic defect. In all chicks of this strain, otoliths were present as a fused crystal mass which contained abnormally large (giant) otoconia. Studies of the formation of such otoliths during embryonic development revealed that from the very earliest stages the otoconia were much larger than normal, and in the saccular and utricular otoliths formed a fused mass. These results are interpreted as supporting a hypothesis of the de novo formation of giant otoconia in this giant-crystal strain as opposed to the recrystallization hypothesis proposed for other, dissimilar mutant mammals and birds which also produce giant otoconia.

Infrared spectroscopy of feline urinary stones revealed that struvite was the main constituent in 77.6% of all concrements. However, only in 30.8% (16/52) of struvite stone patients were any infections of the urinary tract detected. Scanning electron microscopical comparison of non-infected feline struvite stones and human struvite concrements which had grown in the presence of infection revealed clear differences. All the feline struvite concrements were of coarse crystalline construction with the crystalline form typical of struvite. Traces of partial solution and stratification were frequently detected on the crystalline surfaces. The human struvite stones whose growth had been accompanied by infection did not display these features; the predominant structures in these concrements revealed very little evidence of any ordered growth. Examination of the urine and calculation of the relative supersaturation showed that where physiological pH values and physiological concentrations of lithogenic substances were present sterile urine can become supersaturated with struvite. The morphological peculiarities of the feline concrements and the results of urinary analysis indicate slow crystalline growth rates. Phases of growth alternate with periods of stagnation. This process may be influenced by dietary factors. In contrast to this, struvite stone formation in the presence of infection is characterised by rapid growth in continually supersaturated urine.