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B M Chronwall

Publications and source records attributed to B M Chronwall.

69 records · Page 4Linked to original sources

Glial and nonglial neoplasms evaluated on frozen section by double immunofluorescence for fibronectin and glial fibrillary acidic protein.

Antisera against fibronectin (FN) and glial fibrillary acidic protein (GFAP) were used to combined on frozen sections of surgical biopsies to distinguish between astrocytoma and hemangioblastoma, meningioma, or sarcoma. The nonglial neoplasms contained FN in their parenchyma, whereas the gliomas contained GFAP. The immunofluorescent staining procedure takes 10 min. The immunoperoxidase staining for the permanent files takes 30 min. The stains have been used in this institute for more than 1 year, and 26 tumors have been evaluated.

Astrocytoma↗

Glial and divergent cells in primate central nervous system tumors induced by JC virus isolated from human progressive multifocal leukoencephalopathy (PML).

Immunofluorescent stains for fibronectin (FN) and glial fibrillary acidic protein (GFAP) were used in conjunction with routine histologic stains to study tumors induced in squirrel and owl monkeys by JC virus from progressive multifocal leukoencephalopathy (PML). Three varieties of glioma were identified. The first and most common variety was a neoplasm similar to grade 4 astrocytoma in humans. The second had thin, normal-appearing FN-positive vessel walls and a vastly expanded neuroectodermal parenchyma which could not be characterized by routine histologic stains. Anti-GFAP revealed the glial nature of the parenchyma. Isolating glial parenchymal cells from divergent FN-positive cells has become important to neurooncology. This type of tumor may be of particular interest for such isolations due to its high ratio of glial cells to divergent cells. The third variety was not a homogeneous neoplasm. It occurred as focal regions within tumors of the first type, and consisted of giant cells with huge nuclei. These cells resemble the cells of a human giant cell glioblastoma and bear a slight similarity to the bizarre glial cells seen in PML. The rare human giant cell glioblastoma might have an association with JC virus or with PML.

Animals↗

Axosomatic synapses in the visual cortex of adult rat. A comparison between GABA-accumulating and other neurons.

Differences in axosomatic synapses between GABA-accumulating [G(+)N] or non-accumulating [G(-)N] neurons have been investigated in the visual cortex of adult rat. The neurons were classified and localized in light microscopic autoradiograms after [3H]GABA injections. The cells resectioned for electron microscopic identification of type 1 synapses (T1S) and type 2 synapses (T2S). A total of 167 neurons [45 G(+)N, 122 G(-)N] situated in laminae II-VI were evaluated. The two groups of neurons were not uniform populations. G(-)N included both pyramidal and non-pyramidal neurons, whereas no typical pyramidal neurons were found among G(+)N. A total of 691 synaptic contacts was evaluated for these groups of somata. The density of synapses was higher on G(+)N than on G(-)N. This was mainly due to a difference in the number of T1S. On G(-)N the frequency distributions of both types of synapses represented Poisson distributions, indicating that there were stochastic variations around mean values. In contrast, on G(+)N the distribution was exponential which suggests that G(+)N include several subpopulations with different densities of T1S. On all cortical neurons the average density of T2S was 509-60 T2S per 1000 microns2 of soma surface, which resembles the density in the neuropil. In contrast, T1S varied from zero to a mean of 12 per 1000 microns2 on G(-)N and to a mean of 51 per 1000 microns2 on G(+)N, i.e. the density of T1S, unlike T2S, is much smaller on neuronal somata than in the surrounding neuropil. It is suggested that the formation of axosomatic T1S, but not of T2S, is suppressed to a variable degree on almost all cortical neurons. Only on pyramidal neurons does the suppression of T1S seem to be complete.

Animals↗

Characterization and distribution of FMRFamide immunoreactivity in the rat central nervous system.

FMRFamide immunoreactive material (irFMRFamide) was studied in rat brain and gastrointestinal tract. Highest irFMRFamide concentrations were found in tissues of the gastrointestinal tract and, in the brain, highest concentrations were found in the hippocampus, midbrain, brainstem and hypothalamus. High pressure liquid chromatographic characterization of irFMRFamide demonstrated that the immunoreactive material in brain, pancreas and duodenum was different from molluscan FMRFamide but it was also distinct from any known neuropeptide.

Animals↗

Histochemical localization of FMRFamide-like immunoreactivity in the rat brain.

Molluscan cardioexcitatory neuropeptide or FMRFamide is present in the invertebrate central nervous system (CNS) and FMRFamide like peptide has been demonstrated in the mammalian CNS. In this study, the distribution of FMRFamide immunoreactivity was studied in rat brain using the indirect immunofluorescent method. The highest number of FMRFamide staining cell bodies was found in the nucleus (n) arcuatus. N. paraventricularis, n. hypothalamus, n. ventromedialis, n. dorsomedialis and n. tractus solitarii also contained high numbers. FMRFamide positive nerve fibers and terminals were widely distributed. The septal complex contained high densities, especially in n. interstitialis striae terminalis. N. paraventricularis hypothalami, n. paraventricularis, n. hypothalamicus, n. ventromedialis and n. dorsomedialis showed a high to very high degree of immunoreactivity. In myelencephalon, n. tractus solitarii had the densest innervation. Spinal cord had a dense band of FMRFamide positive fibers in lamina I and II of the dorsal horn. The present findings support a neurotransmitter role for a FMRFamide like peptide in the mammalian brain, possibly related to endocrine and autonomic regulation as well as pain modulation.

Animals↗

Presence and distribution of immunoreactive and bioactive FMRFamide-like peptides in the nervous system of the horseshoe crab, Limulus polyphemus.

FMRFamide immunoreactivity was detected in all regions of the Limulus nervous system, including the brain (6.5 +/- 0.6 pg FMRFamide/mg), cardiac ganglion (2.06 +/- 0.67 pg FMRFamide/mg), and ventral nerve cord (5.8 +/- 0.7 pg FMRFamide/mg). The distribution of immunoreactive FMRFamide (irFMRFamide) was mapped by immunofluorescence and the distribution corresponded to regional RIA data. A good proportion of the CNS and cardiac ganglion neuropile contained irFMRFamide, and fluorescent cell bodies were observed in several areas. High performance liquid chromatography (HPLC) was employed to separate and characterize the FMRFamide-like peptides from extracts of Limulus brains. HPLC fractions were analyzed using coincidental radioimmunoassay and bioassay (the radula protractor muscle of Busycon contrarium). There appear to be at least three FMRFamide-like peptides in the Limulus brain, including one similar to clam FMRFamide. FMRFamide acts on Limulus heart in a biphasic manner at relatively high concentrations (10(-5)M), but has no effect on the activity of the isolated ventral nerve cord. These data suggest that in Limulus FMRFamide-like peptides are acting as neurotransmitters, or neuromodulators.

Animals↗

Neuropeptide Y and peptide YY neuronal and endocrine systems.

An extensive system of neuropeptide Y (NPY) containing neurons has recently been identified in the central and peripheral nervous system. In addition, NPY and a structurally related peptide, peptide YY (PYY), containing endocrine cells have been identified in the periphery. The NPY system is of particular interest as the peptide coexists with catecholamines in the central and sympathetic nervous system and adrenal medulla. Evidence has been presented which indicates that NPY may play important roles in regulating autonomic function.

Animals↗

POMC-derived peptide immunoreactivity in neural lobe axons of the human pituitary.

The efferent projections of proopiomelanocortin (POMC) neurons in the arcuate nucleus and nucleus of the solitary tract have been extensively characterized in the rat, but are less well understood in the human brain. We report here that ACTH, alpha-MSH, beta-endorphin, and N-acetyl-beta-endorphin immunoreactive axons are localized in the neural lobe of the human pituitary gland, in congruence with prior evidence that beta-endorphin and other POMC-derived peptides modulate vasopressin and oxytocin secretion.

Adrenocorticotropic Hormone↗