Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:Q9UIJ5 (Rec)
58,342 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A highly specific serotonin binding protein (SBP) has been found in serotonergic neurons in both brain and gut. This protein has an extremely high affinity for serotonin and may be a storage protein. Serotonin is found in many endocrine cells, including parafollicular cells of the sheep thyroid, as well as in neurons. SBP is also present in sheep thyroid. The present study was done to localize the protein in the gland. Thyroid glands were divided into five segments. Concentrations of serotonin and SBP, as well as parafollicular cell volume were measured in each. Serotonin was assayed by enzymatic conversion to melatonin using tritiated S-adenosylmethionine. SBP was assayed by molecular sieve chromatography on sephadex G-50. The relative volume of parafollicular cells was obtained by stereological analysis of electron micrographs. Experiments were also done to demonstrate these cells by histofluorescence and radioautography following incubation with tritiated 5-hydroxytryptophan. Good correlations were found between serotonin and SBP concentrations, and parafollicular cell volume. These peaked in the rostro-central portion of the gland and were minimal at the poles. We conclude that thyroid SBP is probably localized in parafollicular cells.
Anat Rec 1979 Feb
PMID:Localization of a highly specific neuronal protein, serotonin binding protein, in thyroid parafollicular cells. 42 98

Rana pipiens larval beaks of consist of column cells, sheath cells and basal cells which supply cells to column and sheath. Each column consists of disk-like precone cells, cone cells and keratinized cone cells; they are cells in different stages of the process of keratinization. Breaks first appear externally at embryonic stage 24. Epidermal cells align at the tip of the jaw at stage 21. They increase in number and change in shape. Keratinization starts at stage 23. By stage 24, the apical column cells are keratinized and the histological organization is set for the whole larval period. During the larval period, the numbers of column cells increase until stages VIII or IV, stay relatively constant during mid-larval stages, and decrease at late larval stages. The beak is completely shed at stage XX. The widening of the beaks goes on during the entire larval period. Along the cutting edge of the jaw the tooth spikes increase in number and in individual width as the animal grows older and larger. Thyroid hormone causes a premature reduction of the column cell number and a precocious beak loss. The loss of break at metamorphic climax is thyroid dependent event.
Anat Rec 1975 Aug
PMID:Development of beaks of Rana pipiens larvae. 108 23

The effect of aging on the formation of C cell follicles was examined in the thyroid gland of guinea pigs at various ages ranging from 1 to 29 months. The C cell follicles were demonstrated with the immunoperoxidase methods by using anticalcitonin and antisomatostatin antisera and with PAS reaction. They were already detected in 1-month-old guinea pigs but in low number. Thyroid glands from 1- to 14-month-old animals contained only a small number of C cell follicles and did not reveal the age-related increase. In aged guinea pigs (20- to 29-month-old), a dramatic increase of C cell follicles was found, about 13 times as high as the number of other age groups. The C cell follicles through all age groups were present in large clusters of C cells. In the aged guinea pigs, nodular large aggregates of C cells regarded as C cell hyperplasia occurred and numerous C cell follicles were formed in the large cell aggregates. Thus, the conspicuous increase of C cell follicles in aged animals was associated with a proliferative abnormality of C cells. The C cells forming follicles showed moderate to weak immunoreactivity for calcitonin, whereas they showed very intense immunoreactivity for somatostatin. In addition, the colloidlike and flocculent materials stored in the follicular lumina, which were consistently PAS-positive, were weakly immunoreactive to somatostatin but nonreactive to calcitonin.
Anat Rec 1986 Oct
PMID:Age associated increase of C cell follicles in guinea pig thyroid glands. 287 95

The postnatal structural development of the thyroid gland of the Australian native bandicoot, Isoodon macrourus, was monitored and the onset of thyroid function (i.e., the secretion of thyroid hormones) was determined. Thyroid glands were obtained from bandicoots at days 1, 3, 11, 12, 13, 21, 25, 30, 34, 35, 39, 46, 48, 50, 59, 61, 75, 79, 83, and 163 of age and from adult animals, and the tissues were examined with the transmission electron microscope. The thyroid gland of the newborn bandicoot consisted of undifferentiated cells with no lumen. Follicles were first observed at day 12 postpartum, after which time rapid follicular growth occurred. The first signs of thyroid hormone secretion were seen at day 30 postpartum. A peak in thyroid activity seemed to occur around day 50 postpartum, and it correlated with the rapid rate of development of thermoregulatory capacity and hair development which occurred over the last 2 weeks of pouch life.
Anat Rec 1987 Feb
PMID:Thyroid development in the marsupial bandicoot, Isoodon macrourus. 357 35

Thyroids from rat fetuses of different ages (from day 14 to day 19 of gestation) were transplanted to organ culture for 2 days, with or without added thyroid-stimulating hormone (TSH) in the medium. Thyroid tissue from 14-day fetuses that initially consisted of irregularly arranged cell cords did not form follicles when cultured in the presence or absence of TSH. Thyroids from 15- and 16-day fetuses initially consisted of epithelial cell masses. When cultured in the presence or absence of TSH they formed follicles, and a majority stored small amounts of colloid. In thyroid transplants from 17-day fetuses, the response to TSH appeared as a significant increase in the follicular diameter and cell height. Thereafter, in all transplants cultured in the presence of TSH, both the follicular diameter and the cell height were markedly greater than in the transplants cultured in the absence of added TSH. These results suggest that the initial formation of thyroid follicles is independent of TSH and that, once developed, follicles become able to respond to TSH.
Anat Rec 1986 Aug
PMID:Differentiation and thyroid-stimulating hormone (TSH) sensitivity of the fetal rat thyroid in organ culture. 374 Apr 70

Thyroid glands of fetal hypothyroid (hyt/hyt) mice were studied to determine the effects of the mutant gene during embryogenesis. Comparisons of mutant and normal thyroids were made with respect to morphology, iodine-concentrating ability, and glandular thyroxine (T4) content at day 18 of gestation. Fetal hyt/hyt thyroid tissue was properly located, but incompletely differentiated. The mutant thyroid was characterized microscopically by small, poorly developed follicles with colloid diminished in PAS-staining properties. The mutant glands' ability to concentrate iodine was found to be only 5--16% of that exhibited by normal glands. When litters contained both mutant and normal off-spring, the differential iodine-concentrating ability allowed fetuses to be separated into two distinct, nonoverlapping populations. The distribution of fetal mice into high or low iodine-concentrating groups agreed closely with predicted frequencies for normal and mutant phenotypes. Thyroid content of T4 in mutant mice was found to be approximately equal to that found in age-matched normal controls. The poorly developed morphology and deficient iodine-concentrating ability of fetal thyroids from day 18 hyt/hyt mice indicated that the mutant gene acts during the ontogeny of this gland. Although such data are not available on human fetuses affected by thyroid dysgenesis, postnatal hyt/hyt mice display characteristics similar to those of infants born with this form of congenital primary hypothyroidism. Thus, elucidation of the site of mutant gene action in the mouse should contribute to our knowledge of disturbed fetal thyroid development and its implications in the adult mammal.
Anat Rec 1982 Mar
PMID:Defective thyroid ontogenesis in fetal hypothyroid (hyt/hyt) mice. 707 84

Twenty-two subjects in a family with Graves' Disease and 20 normal subjects unrelated to the family were examined for T-cell responses to rec h TSHR-ECD and its synthetic peptides. Seven of the family members and none of the controls responded positively to rec h TSHR-ECD. Peptide 158-176 was the only residue that showed a high percentage of response among family members, no responses in spouses, and a significant difference compared to unrelated controls. Family members under age of 6 did not differ from spouses in response to rec h TSHR-ECD or any individual peptide. Family members ages 6-12 years were significantly different from spouses in response to peptides 30-49, 158-176, and 172-186. The reactivity of adult family members including 3 Graves' patients was significantly different from spouses in response to peptides 44-62, 132-150, 158-176, and 248-263. The responses of female members of the family were higher than that of the male members and significantly different for peptide 272-291. These data suggest that recognition of peptide 158-176 may be an early event in the pathogenesis of the disease and that recognition of both 158-176 and 248-263 residues may be the cornerstone for establishment of the disease.
Thyroid 1996 Dec
PMID:T-cell recognition of residue 158-176 in thyrotropin receptor confers risk for development of thyroid autoimmunity in siblings in a family with Graves' disease. 900 Nov 88

Thyroid-stimulating hormone (TSH) is routinely measured in blood to diagnose thyroid disorders using immunoassays. This study used recombinant TSH (recTSH) as a source of hormonal compound exhibiting a serum-type glycosylation and putatively reflecting physiopathological alterations in TSH polymorphism. Mass spectrometry revealed that in recTSH, both subunits display high-molecular-size glycoforms compared to the pituitary hormone (pitTSH), indicating more complex glycosylation. To determine how changes in TSH glycosylation may affect epitope expression, comparative epitope mapping of rec- and pitTSH was carried out using a panel of ten hormone-specific monoclonal antibodies. Three common epitopes, I, II and III, were identified as common to both preparations and allowed the design of six assays as I/II, II/I, I/III, III/I, II/III, and III/II. Highly sialylated recTSHs were produced by enzymatic remodeling to mimic the hormone circulating in blood and revealed limited expression of epitope I, but enhanced recognition of epitope II. Fractionation on a lentil lectin-Sepharose column allowed selection of non-fucosylated recTSH, thought to be associated with primary hypothyroidism. Recognition of epitope I was not modified by TSH core fucosylation, while epitope III expression was increased in non-fucosylated glycoforms. Taken together, our findings demonstrate that changes in both core and terminal glycosylation alter epitope expression in TSH and thereby induce highly variable antibody recognition, resulting in significant discordances among hormone measurements.
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PMID:Both core and terminal glycosylation alter epitope expression in thyrotropin and introduce discordances in hormone measurements. 1589 74

This study aimed to investigate the association of handedness and position of esophagus with thyroid size asymmetry. One hundred and five healthy subjects were included, and their occurrence of thyroid nodules and position of the esophagus were assessed with ultrasound. Three-dimensional ultrasound was used to measure the volume of the thyroid lobes. The handedness of the subjects was also assessed. Thyroid nodules were found in 43 subjects who were excluded from the study, whereas 62 subjects showed normal thyroid. For normal thyroid, the right lobe (6.8 mL) was significantly larger than the left lobe (5.66 mL) (P < 0.05). Right-handed subjects (mean, 7.11 mL) had a significantly larger right lobe than left-handed subjects (mean, 5.82 mL) (P < 0.05). There was no significant difference in the left lobe volume between right-handers (mean, 5.81 mL) and left-handers (mean, 5.18 mL) (P > 0.05). Subjects with an esophagus deviated to the left (mean, 7.15 mL) had a significantly larger right lobe than those with a centrally located esophagus (mean, 5.7 mL) (P < 0.05). There was no significant difference in the left lobe volume between subjects with different esophageal positions (deviated to left: mean, 5.76 mL; centrally located: mean, 5.19 mL) (P > 0.05). Thyroid asymmetry is associated with the handedness of subjects and the position of the esophagus.
Anat Rec (Hoboken) 2009 Feb
PMID:Asymmetry of thyroid lobe volume in normal Chinese subjects: association with handedness and position of esophagus. 1905 Dec 70

Echolocating bats have adaptations of the larynx such as hypertrophied intrinsic musculature and calcified or ossified cartilages to support sonar emission. We examined growth and development of the larynx relative to developing flight ability in Jamaican fruit bats to assess how changes in sonar production are coordinated with the onset of flight during ontogeny as a window for understanding the evolutionary relationships between these systems. In addition, we compare the extent of laryngeal calcification in an echolocating shrew species (Sorex vagrans) and the house mouse (Mus musculus), to assess what laryngeal chiropteran adaptations are associated with flight versus echolocation. Individuals were categorized into one of five developmental flight stages (flop, flutter, flap, flight, and adult) determined by drop-tests. Larynges were cleared and stained with alcian blue and alizarin red, or sectioned and stained with hematoxylin and eosin. Our results showed calcification of the cricoid cartilage in bats, represented during the flap stage and this increased significantly in individuals at the flight stage. Thyroid and arytenoid cartilages showed no evidence of calcification and neither cricoid nor thyroid showed significant increases in rate of growth relative to the larynx as a whole. The physiological cross-sectional area of the cricothyroid muscles increased significantly at the flap stage. Shrew larynges showed signs of calcification along the margins of the cricoid and thyroid cartilages, while the mouse larynx did not. These data suggest the larynx of echolocating bats becomes stronger and sturdier in tandem with flight development, indicating possible developmental integration between flight and echolocation.
Anat Rec (Hoboken) 2014 Jul
PMID:Ontogeny of the larynx and flight ability in Jamaican fruit bats (Phyllostomidae) with considerations for the evolution of echolocation. 2477 87


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