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Biomedical subjects

J C Adams

Publications and source records attributed to J C Adams.

At least 91 records · Page 5Linked to original sources
PubMed1984

Dorsal nucleus of the lateral lemniscus: a nucleus of GABAergic projection neurons.

Immunocytochemical staining of the dorsal nucleus of the lateral lemniscus with a well characterized antiserum to glutamate decarboxylase reveals that all, or nearly all, cells in this nucleus show immunoreactivity without the use of agents to block axonal transport. Most somata and dendrites are also contacted by immunoreactive axonal endings. It has previously been established that this nucleus is richly innervated by ascending lemniscal fibers and contains different types of neurons that project to the inferior colliculus. One may conclude that this precollicular nucleus is a major GABAergic feedforward inhibitory center in the acoustic pathway.

Animals↗
PubMed1983

Multipolar cells in the ventral cochlear nucleus project to the dorsal cochlear nucleus and the inferior colliculus.

When retrograde markers are placed in the dorsal cochlear nucleus two classes of labeled cells are found in the ventral cochlear nucleus. These are multipolar cells and granule cells. The structure and distribution of labeled multipolar cells greatly resemble those seen following injection of retrograde markers into the contralateral inferior colliculus. When one retrograde marker is placed in the dorsal cochlear nucleus and another simultaneously placed into the contralateral inferior colliculus, large numbers of multipolar cells containing both markers are found in the ventral cochlear nucleus. These findings show that all or most cells in the ventral cochlear nucleus that project to the inferior colliculus also send collaterals to the ipsilateral dorsal cochlear nucleus.

Animals↗
PubMed1983

Cytology of periolivary cells and the organization of their projections in the cat.

Projections of cells located near principal nuclei of the superior olive, periolivary cells, were studied by injecting horseradish peroxidase or fluorescent tracers into the cochlea, cochlear nucleus, and inferior colliculus. At least two distinct cytological classes of periolivary cells were found to project to each of these structures. "Large" and "small" olivocochlear cells were labelled. Their cytology and locations were found to be as had been previously described. Some olivocochlear cells also project to the cochlear nucleus. Other major periolivary cell classes that project to the cochlear nucleus include a lateral group of multipolar cells whose members are located around the ipsilateral lateral superior olive and have coarse, darkly staining Nissl substance. The other major periolivary cell class that projects to the cochlear nucleus is the small cell of the ventral nucleus of the trapezoid body. This cell is characterized by its size and by only one or two intensely staining clumps of Nissl substance. Projections of these cells to the cochlear nucleus is from both sides. Periolivary cells that project to the inferior colliculus include medial and lateral groups. Cells of the lateral group project from both sides. These cells are multipolar in shape and contain lightly staining, flocculent Nissl substance. They are predominantly located immediately ventral to the lateral superior olive. Projections from the medial group are predominantly ipsilateral and arise from the region medial to the medial superior olive. The cells are multipolar and contain clumped Nissl substance. They often lie near "large" olivocochlear cells, which they resemble in Nissl material, but are distinguished from the latter in Protargol material by having ring-type axosomatic endings. The appearance and locations of these six classes of periolivary cells make it possible to recognize them in nonexperimental material and to infer with confidence what their projections are. These results show considerable organization of these previously little understood structures.

Animals↗
PubMed1983

Longevity of selected bacteria in black water.

Twenty four bacteria were killed when exposed to black water. The initial concentration of the organism appeared to have a significant effect upon the survival of the bacteria in six of thirteen cases. Neutralization of black water to pH 7.0 reduced its toxicity to the bacteria studied. Material precipitated during neutralization was also toxic to the bacteria.

Bacteria↗
PubMed1981

Stimulated acoustic emissions in the ear canal of the gerbil.

Ear-canal sound pressure and cochlear potentials were monitored inthe anesthetized gerbil to study the origins of acoustic emissions produced by transient and continuous stimuli. No evidence was found of any delayed emissions (echoes) originating within the cochlea in the acoustic or cochlear microphonic (CM) waveforms. However, strong acoustic and CM distortion products occurred when two primary tones of moderate levels were presented to the ear; the site of origin of these products was traced to the cochlea. Further, the levels of distortion followed a complex time course after anoxia, often becoming stronger after animal death for up to one hour, then decaying to the noise floor of the system. The disappearance of the distortion products was coincident with elimination of both the negative endocochlear potential and the CM response to a fundamental tone.

Acoustic Stimulation↗
PubMed1980

Stabilizing and rapid thionin staining of TMB-based HRP reaction product.

Tetramethyl benzidine (TMB) as a substrate for horseradish peroxidase (HRP) histochemistry offers a great advantage over other substrates in its sensitivity but the reaction product is unstable in alcohol. Immersing TMB-reacted sections in methyl salicylate renders the reaction product stable enough so that exposure to ethanol for 10 min causes no detectable loss of HRP labelled neurons. A rapid thionin stain is introduced which, after stabilizing the TMB-based reaction product in methyl salicylate, causes no detectable loss of HRP labelled neurons. These procedures should prove valuable to users of the popular HRP techniques for studying neural connections.

Benzidines↗
PubMed1980

Crossed and descending projections to the inferior colliculus.

Crossed and descending projections to the inferior colliculus of the cat were studied following injections of horseradish peroxidase. Earlier injections of large (about 1 microliter) volumes and diaminobenzidine histochemistry were fully confirmed with later small volume injections and tetramethylbenzidine histochemistry. Emphasis was placed on describing the cell types projecting to the colliculus and 16 cell types were described. These were found in the contralateral inferior colliculus, the ipsilateral superior colliculus, central gray, substantia nigra, parabrachial region, medial geniculate and bilaterally in the hypothalamus and auditory cerebral cortex.

Animals↗
PubMed1979

Ascending projections to the inferior colliculus.

Cells that send ascending projections to the inferior colliculus were identified following injections of horseradish peroxidase into the colliculus. Labelled cells were found in all subcollicular auditory nuclei. Virtually all cells of the ipsilateral ventral nucleus of the lateral lemniscus and medial superior olive appear to project to the colliculus. Very few cells in these nuclei were labelled on the contralateral side. Heavy labelling on the contralateral side was found in the dorsal nucleus of the lateral lemniscus and cochlear nucleus, with less labelling being found ipsilaterally in these nuclei. The lateral superior olive was approximately evenly labelled on the two sides, with about half the cells from each side projecting to each colliculus. Cells in all periolivary cell groups were labelled, with most being found adjacent to the medial superior olive. An effort was made to identify individual cell types that were labelled and some 24 cell types were identified. In the cochlear nucleus there were marked differences between cell types in the extent of their labelling. Topographic projections matched previously described tonotopic organization of the colliculus and all major subcollicular nuclei except the ventral nucleus of the lateral lemniscus. A description of the cells in the nucleus is provided.

Animals↗
PubMed1978

Anatomy of germinal centers in mouse spleen, with special reference to "follicular dendritic cells".

Lymphocyte proliferation in germinal centers (GC's) is thought to be triggered by antigen retained extracellularly on the surface of special "dendritic" cells. The anatomy and function of these cells have not been studied directly or in detail. We therefore examined mouse spleen GC's developing in response to sheep erythrocyte stimulation. We found that distincitve "follicular dendritic cells" (FDC's) were present in both the GC and adjacent mantle region of secondary follicles. The large, irregularly shaped nucleus, containing little heterochromatin, allowed for the light microscope (LM) identification of FDC's. By EM, the cell was stellate in shape sending out long, thin sheets of cytoplasm which could fold and coil into complex arrays. The processes were coated extracellularly by an amorphous electron-dense material of varying thickness, as well as particulates including variable numbers of virions. The FDC cytoplasm lacked organelles of active secretory and endocytic cells, such as well-developed rough endoplasmic reticulum (RER) and lysosomes. These anatomical features readily distinguished FDC's from other cell types, even those that were extended in shape. To pursue these descriptive findings, we injected three electron-dense tracers i.v. and sacrificed the mice 1 h-10 days thereafter. Colloidal carbon, colloidal thorium dioxide (cThO2), and soluble horseradish peroxidase (HRP) were actively sequestered into the vacuolar system of macrophages but were interiorized only in trace amounts by FDC's. Therefore, FDC's are not macrophages by cytologic and functional criteria. FDC's did display a unique property. Both colloidal carbon and thorium dioxide, which are nonimmunogens, could be visualized extracellularly on the cell surface for several days. The meaning of this is unclear, but the association of colloid with FDC's appeared to slow the movement of particulates through the extracellular space into the GC proper. FDC's were not readily identified in splenic white pulp lacking GC's. They must develop de novo then, possibly from novel dendritic cells that we have identified in vitro (Steinman, R. M., and Z. A. Cohn. 1973. J. Exp. Med. 137:1142-1162).

Animals↗
PubMed1978

Distribution of horseradish peroxidase (HRP)-anti-HRP immune complexes in mouse spleen with special reference to follicular dendritic cells.

The distribution of immune complexes has been studied in mouse spleen stimulated to contain many germinal centers (GC's). Horseradish peroxidase (HRP)-anti-HRP complexes were used as an appropriately precise and sensitive model. We were primarily interested in the relative abilities of three cell types to interact with complexes: lymphocytes, macrophages, and follicular dendritic cells (FDC's). The latter are distinctive, nonendocytic, stellate cells located primarily at the transition of mantle and GC zones of 2 degrees lymphoid follicles (Chen, L. L., J. C. Adams, and R. M. Steinman, 1978, J. Cell Biol. 77:148). Binding of immune complexes to lymphocytes could not be visualized in situ. Macrophages avidly interiorized complexes into lysosomes, but did not retain them extracellularly. In contrast, FDC's could retain HRP-anti-HRP extracellularly under appropriate conditions, but did not endocytose them. Cytochemical reactivity accumulated progressively on FDC's 1--6 h after administration of complexes i.v., remained stable in amount and location for 1 day, and then was progressively lost over a 1- to 5-day period. Several variables in the association of complexes with macrophages and FDC's were pursued. Only 1 microgram of complexed HRP had to be administered to visualize binding to both cell types. Macrophages interiorized complexes formed in a wide range of HRP/anti-HRP ratios, while FDC's associated with complexes formed in HRP excess only. Quantitative studies with [125I]HRP-anti-HRP demonstrated that 20% of the splenic load of HRP associated with FDC's. Complexes formed with an F(ab')2 anti-HRP were distributed primarily in macrophages. When the levels of the third component of serum complement were depleted by prior treatment with cobra venom factor, uptake of complexes by macrophages was reduced some 50% whereas association with FDC's was abolished. The fact that antigen excess complexes are retained extracellularly strengthens the idea that they are immunogenic. Finally, the association of complexes with FDC's seems to retard the entry of antigen into the GC proper.

Animals↗