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Biomedical subjects

B Chronwall

Publications and source records attributed to B Chronwall.

3 recordsLinked to original sources

Sarcoma arising from a gliosarcoma.

An 18-year-old woman with headaches and visual abnormalities was found upon biopsy to have an occipital gliosarcoma, which was treated with irradiation and chemotherapy for a year. Cells in the gliosarcoma tissue were positive for GFAP. At necropsy, only the sarcoma was evident at the site of original surgical removal. The sarcoma had spread widely along meningeal routes, causing the patient's death. The biologic behavior and histologic features of the sarcoma were clearly malignant. Cells cultured from the biopsy specimen maintained features in common with sarcoma.

Adolescent↗

Prenatal and postnatal development of GABA-accumulating cells in the occipital neocortex of rat.

The development of the 3H-GABA-accumulating cells in the neocortex has been followed by light microscopical autoradiography, and after resectioning of the original autoradiograms, by electron microscopy. The validity of the methods used are discussed. The study has been limited to the primary visual cortex and its precursors of rat, from embryonic day (E) 15 to adult. GABA-accumulating cells were found from E 16 onwards in the occipital cortex, which is one to two days after cells arrive in the pallial anlage and one day before the first synapses have been found. Until E 18, the prevalent positions of labeled cells were in lamina I and below the cortical plate. Later, labeled cells also occurred as strands within the cortical plate. During the perinatal period, more and more GABA-accumulating neurons and glial cells began to differentiate and show a characteristic distribution at the periphery of unlabeled cell clusters. From postnatal day 11, no apparent change in density or position of labeled neurons took place. At prenatal stages, two main types of labeled cells were found: 1) Comparatively large cells with rounded nuclei and rough endoplasmic reticulum consisting of narrow, electron-lucent cisterns. These cells were tentatively identified as preneurons. 2) Smaller, polymorphous cells with irregular nuclei and rough endoplasmic reticulum with wide cisterns filled with a dense matrix. These cells are probably precursors of glial cells. Both labeled neurons and glial cells were identified at postnatal stages. In young and adult rats, only neurons to be characterized as nonpyramidal neurons were labeled. Synapses were not found on the perikarya of labeled cells until E 21. Also, in postnatal preparations, labeled neurons showed few axo-somatic synapses. These data were correlated with other events of the structural and functional development of the neocortex. The delay between the appearance of GABA accumulating cells and synaptogenesis indicates that apart from being an inhibitory neurotransmitter, GABA might play a specific morphogenetic role in synaptogenesis. This could even be its primary function during early developmental stages.

Animals↗

A comparison of the anatomical distribution of substance P and substance P receptors in the rat central nervous system.

A comparison of anatomical distributions of substance P (SP) and substance P receptors in the rat central nervous system was performed. SP was localized by microdissection and radioimmunoassay and SP fibers and cell bodies by immunohistochemistry. Receptors for 125I-Bolton Hunter labelled SP (125I-BH-SP) were characterized pharmacologically by a slice binding technique in sections that contained primarily striatum. The receptor was saturable and had an equilibrium dissociation constant (KD) of 0.30 nM and maximum number of binding sites (Bmax) of 37.8 fmol/mg protein. Pharmacological characterization using C terminal fragments and naturally occurring analogues of SP reflected characteristics of the receptor which had been shown previously in bioassays and biochemical assays. Comparison of distribution of SP fibers and cell bodies and SP receptors indicated that there is no consistent relationship between the amount of SP receptor and density of SP fibers or cell bodies in a given region of the brain.

Animals↗