Gene/Protein Disease Symptom Drug Enzyme Compound
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 58,342 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ultrastructural histochemical precedures were employed to determine the carbohydrate components and their contributions to the rodent and amphibian surfactant systems. Zirconium stained the rodent (rat) cytoplasm surrounding the multilamellar bodies, the Golgi, and was associated with the membrane structures of the compact lamellae of alveolar multilamellar bodies. In the rodent and amphibian (Rana pipiens), ruthenium red stain was observed within all tubular myelin surfactant matricies. The "gutters," tubular myelin surfactant matrix, and intratubular myelin surfactant matrix materials all demonstrated a positive reaction product. The periodic acid-chromic acid-silver procedure revealed irregular channels extending from the multilamellar bodies to the surface of the rodent great alveolar pneumocyte. The extra-pulmonary and respiratory surfaces in both species were additionally studied by stereoscanning electron microscopy. The respiratory anatomy of the rodent was corroborated. The amphibian lung demonstrated three orders of septa, and in the expired state, tertiary septal pits. The amphibian primary septa were hollow, blind tubules containing respiratory surfaces.
Anat Rec 1980 May
PMID:The ultrastructural histochemistry and stereoscanning electron microscopy of the rodent and amphibian surfactant systems. 696 19

C-cell complexes are special cell groups consisting of a mass of C-cells associated with other epithelial elements and cysts. They are remnants of ultimobranchial bodies retaining fetal characteristics. In the C-cell complexes there are follicular cells in various stages of differentiation, i.e., the cell clusters not yet organized into follicles, primordial follicles with small lumens and comparatively enlarged follicles storing plentiful amounts of colloid. They have a morphology similar to follicular cells of fetal thyroid glands and react to antiserum to 19S thyroglobulin. In order to determine whether or not the follicles in these complexes have the ability to incorporate radioiodine, autoradiography after a single injection of 125I was combined with immunoperoxidase staining using specific anti-calcitonin, anti-C-thyroglobulin, and anti-19S thyroglobulin antisera. The 19S-positive cells not yet organized into follicles did not take up radioiodine. Primordial follicles showed a heavy accumulation of silver grains over their follicular lumens storing new 19S thyroglobulin as colloid. Comparatively enlarged follicles revealed a strong autoradiographic reaction and their labeling patterns were identical with those of typical thyroid follicles. These results confirm that the follicles in C-cell complexes, as well as thyroid follicles, can incorporate radioiodine and are related to thyroid hormone synthesis. That is, functional thyroid follicles can arise from the ultimobranchial bodies.
Anat Rec 1981 Aug
PMID:Uptake of radioiodine in follicles of dog C-cell complexes studied by autoradiograph and immunoperoxidase staining. 703 Jan 41

An accumulation of cells in early S phase was observed in normal mouse duodenal epithelium studied with flow cytometry (Cheng and Bjerknes, 1982). To determine if this accumulation of cells was the result of a lower rate of DNA synthesis, animals were given a single injection of 3H-thymidine and the epithelium collected one hour later. The epithelium was processed for flow cytometry. Seven sort windows were established in different portions of the DNA histogram. Cells from each window were sorted onto glass slides that were then processed for radioautography. The number of silver grains over the nuclei of each sorted population was counted. It was found that cells in early S phase had significantly fewer grains over their nuclei than did mid- or late-S phase cells. We conclude that the accumulation of cells in early S phase is due, at least in part, to a lower rate of DNA synthesis in early than in mid or late S phase.
Anat Rec 1982 Sep
PMID:Cell flux through S phase in the mouse duodenal epithelium determined by cell sorting and radioautography. 714 79

The fiber connections between the trigeminal mesencephalic nucleus and tract and the trochlear nerve root of 15 cats were examined after silver impregnation of the pontomescencephalic region of the brains. The results revealed that: (a) some of the mesencephalic root fascicles join the trochlear root, (b) some of the mesencephalic root cells contribute their processes to the trochlear root, and (c) some mesencephalic cells are found amidst the fibers of the trochlear nerve during its intrabulbar course. The fibers of the trochlear nerve were counted at certain preselected sites before and after crossing the mesencephalic nucleus. The statistical data obtained indicated that the trigeminal mesencephalic root contributes 4-10% of the fibers of the trochlear nerve, before it crosses the mesencephalic nucleus.
Anat Rec 1981 Dec
PMID:Fiber contribution from the mesencephalic nucleus of the trigeminal nerve to the trochlear nerve in the cat: a histological quantitative study. 734 May 71

The available descriptions of the development of sympathetic innervation of the chick heart conflict with the known sympathetic innervation of the adult chicken heart. The adult heart is innervated by bilateral sympathetic cardiac nerves originating from the first thoracic sympathetic ganglia. These nerves travel lateral and anterior to the lung and join the vagi just before entering the pericardium along the great vessels. Using catecholamine histofluorescence techniques and silver preparations, we have observed the development of the sympathetic cardiac nerves. The sympathetic cardiac nerves arise from the first thoracic sympathetic ganglia on the 7th day of incubation. They grow lateral and then ventral to the developing lungs to join the vagi, and are found in the bulbar region of the heart and atrium on the 10th day of incubation. FLuorescent cells without processes mark the course of the sympathetic cardiac nerves and are present in the bulbar region on the 10th day and thereafter. Sympathetic ganglion cells lose their fluorescence between day 8 and day 16 of incubation. This is presumably due to dilution of the transmitter in the rapidly increasing volume of cytoplasm in the sprouting neurons. Small intensely fluorescent (SIF) and adrenal medullary cells do not undergo a diminution of fluorescence during this period. SIF cells appear well differentiated at 16 days.
Anat Rec 1980 Mar
PMID:Developing innervation of the chick heart: a histofluorescence and light microscopic study of sympthetic innervation. 740 24

Ascending axons in the dorsal column of garter snakes were examined following hemisection of the spinal cord at segment levels 2, 3, 4, 11, 13, and 31. After postoperative survival periods of 11 to 28 days, sections of the spinal cord and brain were processed with a silver method to demonstrate degenerated axons and preterminals. The study demonstrated that most ascending degenerated axons are located in the outer half of the dorsal column. The somatotopic pattern of ascending fibers is evident, whereby dorsomedial fibers are primarily of caudal origin and the more dorsolateral axons are from rostral cord segments. Rostral to segment 31, all spinal segments appear to project to a strip of dorsal column adjacent to the dorsal median septum. From the septum, axons descend to terminate somatotopically on cells of the nucleus of Bischoff located caudal to the obex of the medulla. Dorsal column degeneration ascends to the level of the dorsal column nuclei, where most fibers terminate. Degeneration from caudal cord segments terminates on caudo-medial cells of the dorsal column nuclei, while rostral cord segments project to rostro-lateral cells. The dorsal column nuclei consist of an expanded lateral part between tractus descendens trigemini and the vago-solitary complex, and a contiguous, thin medial lamina of cells dorsal and medial to the vagal nuclei. The somatotopic pattern of degeneration in the dorsal column nuclei, probably of dorsal root origin, follows the mammalian organization, which suggests that the garter snake has primitive nuclei gracilis and cuneatus. Other terminal sites of degenerating fibers, although probably of spinal gray origin, are nucleus commissura infima, nucleus descendens vestibuli, and area postrema.
Anat Rec 1980 Jan
PMID:Ascending projections of the dorsal column in a garter snake (Thamnophis siritalis): a degeneration study. 741

The purpose of this investigation was to test the hypothesis that activation of the immune system in rats will lead to changes in the density of innervation in lymph nodes. In order to reduce the variability between animals, the rats were reared under sterile conditions and immunostimulation was effected by subcutaneous application of bovine albumin in a region draining to the axillary lymph nodes of both sides. Control animals received an equivalent application of sterile physiological saline. The animals were sacrificed 10 days and 27 days and 4 months after immunostimulation. The nerves in the axillary lymph nodes were quantified by light microscopy in silver impregnated sections and at the ultrastructural level on ultrathin sections. The survival times were chosen so that the first group was in the ascending phase of antibody production, the second group at the peak, and the third group in the declining phase. Both at the light and ultrastructural levels, there were statistically significant differences in the density of innervation of medulla between the groups, with a particularly pronounced increase in the group 4 months after immunostimulation. At the ultrastructural level, there was also an increase in the density of incompletely ensheathed axonal profiles in the parenchyma of the medulla, while the nerves associated with blood vessels were not increased. We conclude that immunostimulation leads to morphological changes in the innervation of the medulla of axillary lymph nodes, that are consistent with the concept of functional activation of the autonomic nervous system through the immune system.
Anat Rec 1994 Feb
PMID:Plasticity of innervation of the medulla of axillary lymph nodes in the rat after antigenic stimulation. 815 7

SP-10 is a sperm-specific, intra-acrosomal protein that is considered to be a vaccine candidate for immunocontraception. In the present study, in situ hybridization with biotin and 35S labeled riboprobes was used to determine the pattern of SP-10 mRNA expression in human testes. Both methods demonstrated SP-10 mRNA primarily in round spermatids found in stages I, II, and III of the seminiferous cycle. Morphometric analysis of silver grains with the 35S-labeled probe showed less SP-10 mRNA in spermatids at stages IV, V, and VI than in previous stages, and rarely was label found in spermatogonia or spermatocytes. The expression of SP-10 mRNA first appeared at stage I coincident with the appearance of the protein, which was shown previously to persist in the acrosomal matrix throughout spermiogenesis. The decrease in SP-10 mRNA occurred when spermatids underwent polarization, nuclear condensation, and elongation. The appearance of SP-10 mRNA in round spermatids suggests that increases in SP-10 transcription or SP-10 mRNA stability or both occur as spermatids develop from the Golgi phase to the cap phase. The subsequent decline of SP-10 mRNA, despite the persistence of the SP-10 protein in all spermatids, suggests that a decrease in SP-10 transcription or an increase in mRNA degradation occurs when spermatids elongate.
Anat Rec 1993 Aug
PMID:Stage-specific detection of mRNA for the sperm antigen SP-10 in human testes. 837 86

Variously fixed, wax-embedded lung and gastrointestinal serial tissue sections from newborn to adult cats were stained with hematoxylin-eosin (H&E), Grimelius' silver, and immunohistochemical techniques using antisera to protein gene product (PGP) 9.5, a neuron-specific protein under strong evolutionary constraints. PGP 9.5 is revealed as a pan-neuroendocrine marker useful for tracing the pulmonary diffuse neuroendocrine system (PDNES) and studying the relationships between neuronal and neuroendocrine elements at various stages of life. Its occurrence is also compared in the pulmonary and the gastrointestinal tract. In spite of a close resemblance to already described neuroepithelial bodies (NEB) of other mammals, cat NEB feature typical constitutional and distributional difference, illustrating interspecies differences. The number of PGP 9.5 immunopositive pulmonary neuroendocrine cells declines gradually after 3 weeks and throughout adult life. Immunoreactivity in neuronal elements is lost after 1 week of age. In gastrointestinal tissues, only neuronal elements immunostain, suggesting functional variations or a separate embryological origin for enteroendocrine cells.
Anat Rec 1993 May
PMID:Immunocytochemical expression of protein gene product (PGP) 9.5 in the cat bronchopulmonary neuroendocrine cells and nerves. 850 6

The presence of porcine reproductive and respiratory syndrome (PRRS) virus in pig meat was assessed in samples collected from experimentally infected pigs and from the carcases of pigs from infected herds at an abattoir. In the experimental study, pigs approximately six months old were inoculated with two isolates of PRRS virus and tissue samples were collected seven and 14 days after inoculation. At seven days, PRRS virus was recovered from lungs, tonsils, lymph nodes and muscle tissues, and viral antigens were detected by immunogold silver staining (IGSS) in formalin-fixed lungs, tonsils and scattered cells in muscle tissues. Neither PRRS virus nor antigens were detected in muscle tissue samples collected 14 days after inoculation. In the abattoir pigs, attempts were made to isolate PRRS virus from a total of 44 samples of muscle tissue, collected as pools, from the carcases of 44 pigs originating from seropositive herds. No PRRS virus could be isolated on porcine alveolar macrophages from these 44 muscle tissue samples and no PRRS virus antigens could be detected by IGSS in the formalin-fixed tissue samples. Although the results of experimental infections indicated that PRRS virus may be recovered from muscle tissues early after infection with the virus, the presence of PRRS virus in muscle tissues from carcases of slaughter pigs previously exposed to the PRRS virus could not be demonstrated.
Vet Rec 1995 Nov 25
PMID:Evaluation of the persistence of porcine reproductive and respiratory syndrome virus in pig carcases. 864 34


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