Uterine zonal anatomy as visualized on T2-weighted (repetition time, 2,500 msec; echo time, 80 msec) magnetic resonance (MR) images consists of a high-intensity central (endometrial) zone, a subjacent low-intensity junctional zone of myometrium, a moderately intense zone of myometrium, and a thin, low-intensity subserosal zone of myometrium. To better define the histologic correlates of these diagnostically significant zones, T2-weighted MR images of 17 in vivo and 13 extirpated human uteri were compared with histologic sections of 17 uteri stained with hematoxylin-eosin, Mallory trichrome, and immunofluorescence staining for actin. Morphometric and electron microscopic observations of uterine surgical specimens were also made. The observations indicate that both the junctional zone and the subserosal zone consist of compact smooth muscle fibers with little extracellular matrix compared with the myometrium proper. Also, the junctional zone is divided into a compact region and a transitional region. The compact region correlates well with the hypointense MR appearance of the junctional zone.

Legionella pneumophila (Lp) grow in cultures in human, guinea pig, and mouse macrophages from A/J strain mice. Because exudate macrophages from this strain of mice have been reported deficient in responsiveness to lymphokines, we thought it of interest to document the extent of responsiveness to interferon-gamma in the context of growth restriction of Lp. Peritoneal exudate macrophages were obtained from A/J mice and cultured in either the presence or absence of recombinant interferon-gamma. These cultures were then infected with Lp and the extent of bacterial growth estimated 48 hr later by means of a colony-forming unit (CFU) assay and electron microscopy. Interferon-gamma treatment significantly restricted the number of CFUs in the culture at concentrations as low as 20 U/ml, but did not affect the uptake of bacteria by macrophages. Furthermore, treatment with interferon induced morphological changes consistent with activated macrophages. The involvement of oxygen-dependent mechanisms in phagocyte killing and growth restriction was examined by the use of inhibitors such as superoxide dismutase (SOD) and catalase. Neither one of these inhibitors of toxic oxygen metabolites affected the interferon-gamma-induced suppression of Lp growth. These results suggest that although thioglycolate-induced exudate macrophages from A/J mice support the growth of Lp, these cells readily respond to the activating influence of interferon-gamma. Furthermore, lymphokine treatment does not inhibit Lp uptake by macrophages and apparently restricts the growth of bacteria by mechanisms independent of the activity of toxic oxygen metabolites.

Currently, the diagnostic interpretation of magnetic resonance (MR) images requires that radiologists integrate specific tissue contrast information from several different images obtained at the same anatomic slice position. Each of these images has its own unique tissue contrast patterns which are based on the image acquisition parameters (pulse sequence) selected. The complex contrast patterns observable in these images reflect the inherent biophysical characteristics of the tissues and fluids present in the imaged section. In an effort to increase the diagnostic accuracy and efficiency of MR image interpretation, we have generated color composite images from quantitatively analyzed achromatic MR images of the brain, obtained while utilizing different pulse sequences. By using a DEC MicroVAX II computer with Interactive Digital Language (IDL), this color display method has been applied to images obtained from General Electric Signa and Siemens Magnatom imagers. For this study, our image sets included T1-weighted, T2-weighted, and proton density spin echo sequences as well as both high and low flip angle gradient echo sequences. Advantages of our color composite methods, in contrast to many other image processing techniques that have been described, are that minimal information is lost, computer misclassification of tissues is avoided, and the conspicuity of specific tissues is enhanced. Furthermore, with this method it is possible to produce composite images whose color renditions approach a natural anatomic tissue appearance. Availability of these color composites to radiologists may improve the efficiency and accuracy of the diagnostic interpretation of MR images.

Legionella pneumophila infection of macrophages from permissive guinea pigs and from AIJ mice compared with infection of cells from nonpermissive BDF, mice was studied by electron microscopy. The cells from the BDF1 mice were nonpermissive for legionella growth in vitro and showed few if any bacteria in phagosomes by electron microscopic examination. Similar electron micrographic examination of macrophages from A/J mice permissive for legionella growth showed numerous intact intracellular bacteria within 24 to 48 h of culture and the transition of intracellular bacteria from localization in a few large vacuoles early in the course of infection to later localization in areas surrounded and studded by ribosomes. These electron microscopic observations were similar to those seen in the case of guinea pig macrophages infected with legionellae. Biochemical studies of macrophages from permissive versus nonpermissive animals showed little or no differences in respiratory burst and lysosomal enzyme activity for macrophages from all animals tested. However, when zymosan was used as a stimulant, macrophages from the nonpermissive mouse strain produced a larger amount of H202 and