Tetanus in New York State, excluding New York City. Incidence and control.
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Humans↗
Biomedical subjects
R M Albrecht
Publications and source records attributed to R M Albrecht.
Distribution and movement of membrane-associated platelet glycoproteins: use of colloidal gold with correlative video-enhanced light microscopy, low-voltage high-resolution scanning electron microscopy, and high-voltage transmission electron microscopy.
Scanning electron microscopy (SEM), especially low-voltage (1 KeV) high-resolution SEM, can be used in conjunction with stereo pair high-voltage (1 MeV) transmission electron microscopy (HVEM) of whole spread cells or thick sections effectively to correlate surface structure with internal structure. Surface features such as microvilli, pits, pseudopodia, ruffles, attached virus, and other surface-related morphologic characteristics can be identified using SEM, while underlying cytoskeletal structure and organelle organization can be viewed by HVEM of the same preparation. However, the need to "prepare" cells for electron microscopy precludes observation in the living state. The use of several types of video-enhanced light microscopy (VLM) permits observation of living cells such that certain surface and internal features can be observed at a relatively high level of resolution or detection. Thus, changes in living cells can be followed, and at appropriate times the cells may be chemically fixed or rapidly frozen and prepared for ultrastructural examination by electron microscopy. We have utilized VLM in conjunction with SEM and HVEM to correlate changes in shape and surface structure with changes in the internal structure of platelets. In addition, we have found it advantageous to use colloidal gold-labeling procedures, because these markers are detectable by all three forms of microscopy. Using this approach we have labeled platelet membrane GPIIb/IIIa, a receptor for RGD-containing adhesive proteins, with gold-fibrinogen or gold-anti-IIb/IIIa. The initial binding and subsequent movement of gold-fibrinogen-IIb/IIIa complexes in living platelets was followed by VLM. The movement of individual labels could be mapped. Subsequent observation by low-voltage (1 KeV) high-resolution SEM and HVEM permits visualization of the same individual receptors tracked by LM. The final position on the membrane or the position-in-transit when fixative was added was determined relative to surface ultrastructure (SEM) and internal, particularly cytoskeletal, ultrastructure (HVEM).
Biological Transport↗
Scanning electron microscopy after cytologic examination of urinary cells: lack of diagnostic advantage using combined microscopy.
A simple method for combined light microscopy (LM) and scanning electron microscopy (SEM) of urinary sediment is described. Spontaneously voided cells were routinely collected onto a filter for cytologic study. Individual cells were photographed and demarcated by an ink grid pattern and puncture marks in the filter. The filter was prepared for SEM. The cells that were studied by LM could be readily located and examined by SEM. This study showed the importance of identifying individual cells before observation by SEM since cells with similar appearances by LM may have markedly different features by SEM, and vice versa. The results obtained in a series of patients with transitional-cell bladder carcinoma indicate that degenerative changes in voided urothelial cells negate the utility of SEM as a routine screening tool.
Carcinoma, Transitional Cell↗