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S Wray

Publications and source records attributed to S Wray.

At least 91 records · Page 5Linked to original sources

Contribution of extracellular calcium to intracellular pH-induced changes in spontaneous force of rat portal vein.

Normal spontaneous mechanical activity of isolated rat portal vein is critically dependent on external calcium as a source of contractile activation and this force is modified by alteration of intracellular pH. We have studied the involvement of the extracellular calcium pool in intracellular pH-induced changes in force. Intracellular pH was changed, at constant external pH, by NH4Cl application and withdrawal in bathing [CaCl2] varying between 3 and 0 mM, and manoeuvres were performed in the presence and absence of either the intracellular calcium mobilizer caffeine or the calcium channel blocker nifedipine. The results indicate that alteration of spontaneous force with intracellular pH has an absolute requirement for calcium entry from outside and calcium release from caffeine-sensitive intracellular stores.

Ammonium Chloride↗

Effects of insulin-like growth factors I and II and insulin on the immortalized hypothalamic GTI-7 cell line.

Insulin and insulin-like growth factor I (IGF-I) participate in energy metabolism, regulate cellular growth and differentiation, and are thought to act locally in a paracrine manner through specific receptors. Systemic levels of these peptides in humans and primates are directly associated with levels of activity of the reproductive axis. To date, it is unclear whether these peptides participate in reproductive function by acting at the level of the GnRH neuron. In this study we examined the effects of IGF-I, IGF-II and insulin on immortalized GnRH-secreting neurons, the GTI-7 cell line. The GTI-7 cells expressed all three members of the insulin receptor family as determined by analysis of 125I-IGF-I, 125I-IGF-II and 125I-insulin binding sites. Insulin receptors bound insulin, IGF-II and IGF-I with a ratio of potency of 1:5:20. IGF-I and IGF-II receptors bound both IGF-I and IGF-II. The ratio of potency of IGF-I/IGF-II was 1:5 for the IGF-I receptor and 100:1 for the IGF-II receptor. The binding characteristics of the growth factors at 22 degrees C suggested the possibility that these cells may secrete IGF binding proteins. To ensure that changes in GnRH levels in the media were due to secretion and not to changes in cell number, the mitogenic effect of these peptides on GTI cells was evaluated. Both insulin and IGF-I were strong mitogens (48-hour incubation), restoring cell number to that of serum-replete cultures at a dose of 0.1 ng/ml. A 100-fold higher dose of IGF-II was required to produce a similar level of mitogenicity, implicating an action through the IGF-I and/or insulin receptor. Due to these mitogenic effects, the effect of insulin, IGF-I and IGF-II on GnRH secretion was studied after short-term exposure. Insulin and IGF-I did not affect GnRH secretion, but IGF-II had a biphasic effect on GnRH release after 2 h of incubation (a maximum stimulatory effect occurred with a 0.1 ng/ml dose). In order to examine the signal transduction mechanism, the role of cytoplasmic calcium mobilization in IGF-II-induced GnRH secretion was examined in single cells using calcium imaging. The effect of IGF-II on GnRH secretion appeared to operate via a calcium-independent mechanism. The studies document an insulin/IGF system in the GTI-7 neuronal cell line and show that insulin and IGFs can exert direct effects on the immortalized GnRH neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Binding Sites↗

The relationship between plasma urea levels and some muscle trimethylamine levels in Xenopus laevis: a 31P and 14N nuclear magnetic resonance study.

Urea is known to be disruptive to proteins, yet high levels occur in a variety of tissues. It has been suggested that trimethylamines counteract the effects of urea on protein. We have, therefore, directly investigated whether elevating tissue urea levels produces an increase in trimethylamine concentrations by using 31P and 14N nuclear magnetic resonance (NMR) spectroscopy to detect two trimethylamines (glycine betaine and glycerylphosphorylcholine) in intact, living gastrocnemius muscle from Xenopus laevis. Xenopus laevis naturally elevates its tissue urea levels under dry conditions. This ability was used to obtain plasma urea levels ranging from 1 to 110 mmol l-1. This procedure did not alter pH or levels of ATP or phosphocreatine in the muscles, but did raise trimethylamine levels. We find that there is a significant relationship between plasma urea concentrations and the trimethylamine levels studied. This relationship was, however, limited to the lower range of urea levels. We propose that other trimethylamines or mechanisms come into play at urea concentrations above 20 mmol l-1.

Animals↗

Functional effects of intracellular pH alteration in the human uterus: simultaneous measurements of pH and force.

Changes in intracellular pH have differing effects on contraction in different types of muscle, and between species. Because of the large number of women requiring a caesarean section due to failure to progress in labour, it is important to know how the human myometrium responds to the changes in intracellular pH that may occur during labour. The pH-sensitive dye, carboxy-SNARF, was used to measure intracellular pH in small strips of human myometrium. Intracellular pH and tension were simultaneously recorded in pregnant and nonpregnant tissue. Intracellular pH was altered by the addition of weak acids and bases. Intracellular alkalinization caused an increase in the frequency and amplitude of contractions. Intracellular acidification led to an initial increase in the frequency and/or the amplitude of the contractions, followed by abolition of contractions. Alterations in intracellular pH had profound effects on contraction in human uterine smooth muscle. Possible mechanisms are discussed whereby pH could influence force production, and changes in contraction are related to the speed and extent of the change in intracellular pH.

Adult↗

Bombesin receptor gene expression during mammalian development.

Mammalian bombesin-like peptides (gastrin-releasing peptide [GRP] and neuromedin B [NMB]) and their receptors (GRP-R and NMB-R) can stimulate growth of cultured cells, and have been shown to be part of an autocrine growth regulatory network in some human small cell lung carcinoma cells. Given the connection between bombesin receptor expression and bombesin-mediated growth regulation in cultured cells, we were interested in investigating the possibility that bombesin peptides and their receptors might be important for normal growth and differentiation during development. As a first step, we examined the distribution of expression of GRP-R and NMB-R mRNA during rat embryonic development to identify changing spatio-temporal patterns of gene expression. In situ hybridization studies show that GRP-R mRNA is expressed at early embryonic stages in various locations of the nervous, urogenital, respiratory, and gastrointestinal systems. In contrast, the distribution of expression of NMB-R mRNA is more limited (upper gastrointestinal tract, bladder, and central nervous system) and is observed at later embryonic stages. In most locations, receptor mRNA levels increased steadily throughout development after onset of expression. However, transient GRP-R mRNA expression is observed in the posterior pituitary where expression increases from embryonic day 12 to 20, and abruptly disappears at birth. These studies suggest that appropriate development of several organ systems, in particular the posterior pituitary, may involve GRP-R-mediated signaling. We plan to test this hypothesis using gene targeting to inactivate the GRP-R gene in the mouse.

Animals↗

Abolition of contractions in the myometrium by acidification in vitro.

Uterine dystocia, often of unknown cause, remains one of the commonest causes of emergency caesarean section. We have tested the hypothesis that small acidic changes in pH, that can occur during labour contractions, can decrease contractions and contribute to dystocia. We simultaneously recorded intracellular pH (pHi) and force in human myometrium: acidification abolished contractions. Such effects of pHi on uterine contractile activity may be of clinical significance. Blood flow reduces during each uterine contraction; the resulting fall in pHi could lead to inefficient uterine action in some labours and failure to progress (ie, dystocia).

Adult↗

An in vivo study of the effects of ischaemia on uterine contraction, intracellular pH and metabolites in the rat.

There are no data concerning the functional or metabolic effects of hypoxia in vivo in smooth muscle. We have therefore used 31P-NMR spectroscopy and intra-uterine pressure measurements to examine simultaneously, in vivo, the effect of ischaemia on uterine metabolites, intracellular pH (pHi) and force. A 1-2 cm portion of uterus from day 1 postpartum anaesthetized rats was exteriorized and an NMR surface coil placed on it. A balloon catheter in the uterine lumen recorded intra-uterine pressure changes from the same area. Reversible occluders were placed around the uterine artery. Occlusion produced a decrease and then abolition of contractions, within 10 min. In four of five animals contraction was abolished within 2 min. Upon reperfusion force was rapidly restored (1 min), in all preparations. The mean level of force was significantly above control (pre-occlusion) 20-30 min after reperfusion. The NMR data showed a significant fall in [ATP] (28%) and [phosphocreatine] (34%) during occlusion. Inorganic phosphate doubled in concentration during this period. Metabolites recovered slowly upon reperfusion, taking 20-30 min to return to pre-occlusion levels. The mean pHi fell from 7.32 to 7.00 upon occlusion and was rapidly reversed upon reperfusion. The changes in pHi closely correlated with the changes in uterine force. Decreases of pHi of a similar magnitude in vitro have previously been shown to abolish contractions; thus it is suggested that during ischaemia in vivo the depression of contraction is caused by the large fall in pHi.

Animals↗

A comparison of the effects of intracellular and extracellular pH on contraction in isolated rat portal vein.

1. The effects of changes in extracellular and intracellular pH on spontaneous contractile activity in isolated rat portal vein have been investigated. 2. Small strips of portal vein were loaded with the pH-sensitive fluorophore carboxy-SNARF and intracellular pH (pHi) and contraction were measured simultaneously at 37 degrees C. The tissue was superfused with oxygenated, Hepes-buffered solutions at pH 7.4. Intracellular pH was altered by isosmotic substitution of weak acids or bases. External pH (pHo) was altered by addition of strong acid or base to the solution. 3. The mean resting value of pHi was 7.06 +/- 0.03 (n = 28). Alteration of pHi led to changes in spontaneous activity. Addition of butyrate (20 mM) reduced pHi by 0.18 +/- 0.01 pH units (n = 8). Decreasing pHi produced an early, brief increase in contractile activity followed by a longer lasting decrease or even abolition of contraction. 4. Addition of 20 mM trimethylamine or NH4Cl increased pHi by around 0.2 pH units and produced an early transient decrease in contractile activity followed by a later maintained increase, both in frequency and magnitude. Removal of base produced a rapid rebound decrease in pHi which was associated with a further transient increase in contractile activity followed by decreased activity. The effects of base on both pHi and contraction were concentration dependent over the range investigated (2.5-30 mM). 5. Alteration of pHo produced a change in pHi in the portal vein. The pHi change was rapid compared to other non-vascular cells (about 1 min to half-maximal response).(ABSTRACT TRUNCATED AT 250 WORDS)

Ammonium Chloride↗

LHRH cells migrate on peripherin fibers in embryonic olfactory explant cultures: an in vitro model for neurophilic neuronal migration.

Luteinizing hormone releasing hormone (LHRH) neurons arise from progenitor cells in the olfactory placode. During prenatal development, these cells migrate via neurophilic interactions, in track-like arrangements along axons of the olfactory complex. The mechanisms by which these cells attain an adult-like distribution are unknown. In this study, we established an in vitro, embryonic mouse olfactory explant model to examine the factors directing LHRH cell migration. Cultures were generated from E11.5 embryos and maintained for up to 3 weeks. Typically 20-50% (160-400 LHRH cells) of the total LHRH neuronal population survived and maintained gene expression in these explants. Fibronectin and laminin staining delineated substratum producing cells which concentrically spread, from Days 1-7, from the periphery of the entire explanted tissue. In contrast, LHRH cells emigrated exclusively from inside olfactory pit areas to the surface of the culture after 3 days. The relationship between groups of LHRH cells emerging from bilateral olfactory pits was not random, but highly organized; in 93% of the cultures examined, the angular relationship between these groups was 180-270 degrees. After 5 or more days in vitro, LHRH cells were found in directional tracks similar to those observed in vivo forming a continuum from the olfactory pit out onto the substratum, where many bipolar LHRH cells were discretely located. The maximum distance away from the olfactory pit that LHRH cells were detected was 0.9 mm, which is compatible with the distance traversed by LHRH cells through the nasal region in vivo. The reproducible spatiotemporal appearance of LHRH cells was unrelated to the concentric spread of the fibronectin and laminin producing cells of the explant. Taken together, these data indicate that LHRH cells migrated directionally in these explants and that the molecular cues governing the initial migration of these neurons remained intact in this system in the absence of brain tissue. Double-label immunocytochemistry indicated that at least three populations of neuronal fibers existed in the explants: N-CAM-positive, peripherin-positive, and N-CAM/peripherin-positive. Although all three fibers groups showed highly organized spatiotemporal distribution patterns, only peripherin-positive fibers correlated with the location of LHRH cells. LHRH cells were always preceded by, and in close association with, peripherin-positive fibers. We hypothesize that signals arising from the peripherin-positive axons provide the appropriate guidance cues to LHRH cells as they emigrate from the olfactory pit.

Animals↗

A subset of peripherin positive olfactory axons delineates the luteinizing hormone releasing hormone neuronal migratory pathway in developing mouse.

Luteinizing hormone releasing hormone (LHRH) neurons in the CNS are derived from cells of the olfactory placode and thereafter migrate from the olfactory pit into the diencephalon. In this study, we examined embryonic LHRH neurons and the LHRH migratory pathway for several markers. During development, N-CAM and peripherin mRNA were expressed by olfactory epithelia, but not by LHRH cells. In nasal regions, olfactory axons were not immunostained by laminin or fibronectin antibodies, but were robustly peripherin and N-CAM immunoreactive. Although the majority of these axonal tracks entered the developing olfactory bulbs, a small population of peripherin positive but N-CAM negative axons turned caudally into the developing forebrain. LHRH cells were consistently juxtaposed to these axons. We propose that this peripherin positive/N-CAM negative fiber track is the anatomical pathway upon which LHRH cells migrate from the olfactory pit into the diencephalon.

Animals↗

Steroid hormone regulation and tissue-specific expression of the human GnRH gene in cell culture and transgenic animals.

In order to study the molecular mechanisms involved in the control of GnRH gene expression, the human GnRH gene was cloned and characterized. The gene was expressed in cells obtained from CNS tumors in transgenic mice generated utilizing 1131 bp of 5' flanking GnRH DNA fused to the simian virus 40 large T antigen. We have shown a stimulatory estrogen response element in the human GnRH gene by transient transfection studies. DNase I footprinting and an avidinbiotin DNA binding assay demonstrated that the human GnRH gene bound ER. The GN cell line was found to have nuclear ERs utilizing an 125I estradiol binding study and by in situ hybridization histochemistry. In order to study GnRH expression in vivo, either 5000 or 484 bp of GnRH flanking DNA was fused to the luciferase (Luc) reporter gene, and transgenic mice generated. Expression in the transgenic animals was found in the hypothalamus of animals bearing the -5000Luc transgene, but not in animals bearing the -484Luc transgene. The transgenic mice expressing the -5000Luc gene were gonadectomized resulting in a 20-30% increase in hypothalamic Luc expression in the males and a 65% increase in females, while mice who were gonadectomized and replaced with testosterone (males) or E2 (females) showed a 50% decrease in Luc expression over control levels. Thus, these studies present in vitro evidence of E2 modulation of GnRH gene expression and an in vivo model in which sensitive studies of GnRH regulation and expression can be performed.

Animals↗

A quantitative study of the relation between intracellular pH and force in rat mesenteric vascular smooth muscle.

Strips of rat mesenteric artery were loaded with carboxy-seminaphthorhodafluor (SNARF) to measure intracellular pH (pHi) and force simultaneously. pHi was altered by using weak acids and bases. Alkalinization produced an increase in force. For equal elevations of pHi a greater and faster increase of force was obtained in depolarized (high K+) than in non-depolarised preparations. Acidification produced little change in force unless the tissue was contracted (high-K+), in which case it elicited relaxation. Examination of the relationship between pHi and force in depolarized preparations showed that acidification produced a greater change in force than alkalinization. Removal of weak bases produced a transient acidification that was accompanied by a fall in force in all preparations. This was followed by a secondary contraction in depolarized preparations during the period over which pHi was acidic and being restored to resting values. Some preparations demonstrated a hysteresis in the relation between pHi and force. It is concluded that the relationship between pHi and force in mesenteric vascular smooth muscle is not constant but depends on the previous history of the preparation, and may involve differences in the interactions between H+, Ca2+ and the contractile machinery.

Ammonium Chloride↗

Differential effects of external pH alteration on intracellular pH in rat coronary and cardiac myocytes.

Changes in extracellular pH (pHo) induce changes in the intracellular pH (pHi) of cardiac myocytes that are slow and attenuated. Little however is known about the effects of changing pHo on the pHi of the coronary smooth muscle cells. We have therefore directly compared the effects of altering pHo on pHi of both coronary and cardiac myocytes. Carboxy-SNARF was used in single cells to measure pHi. Alteration of pHo caused corresponding changes in pHi that were large (70-80% of pHo) and rapid in coronary myocytes compared to cardiac myocytes. In contrast, changes of pHi produced by weak acids or bases produced similar pHi responses in both types of cells. It is suggested that the differential effects of pHo on coronary and cardiac cells may be functionally significant, as it will allow rapid alteration of coronary perfusion to meet tissue needs, while maintaining cardiac output.

Animals↗

Changes in human and rat uterine phosphoethanolamine and taurine with pregnancy and parturition.

Phosphoethanolamine and taurine have been identified in uterine extracts from rat and, for the first time, human tissue. The concentration of phosphoethanolamine [PEtn] determined by HPLC and 31P NMR spectroscopy, increased markedly (40%) within the first 6-12 h following parturition in rats, suggesting a role in involution. It appears that changes in [PEtn] account for the changes in the NMR phosphomonoester peak previously reported. A significant fall in [PEtn] was found in the human myometrium with pregnancy. Taurine was found in high concentrations in the rat and human uterus but decreased with pregnancy. The possible functional significance of these changes is discussed.

Adult↗

Developmental and gestational changes of phosphoethanolamine and taurine in rat brain, striated and smooth muscle.

Concentrations of taurine and phosphoethanolamine in rat smooth (intestinal and uterine), skeletal and cardiac muscle, and brain have been determined, using high-performance liquid chromatography (HPLC), to examine possible interrelationships in their tissue content. Concentrations were determined in fetal and neonatal samples, as well as in adult tissue, to investigate whether phosphoethanolamine and taurine levels are influenced by developmental state. The effect of gestational state was also studied. A marked decrease in cerebral phosphoethanolamine concentration during development was found together with a concomitant decrease in striated muscle but not in the two smooth muscles studied. A rise in uterine phosphoethanolamine during the early postpartum period confirmed previous NMR data. This occurred only in the uterus, suggesting it is specific to the process of involution within the myometrium. Taurine concentrations showed no consistent pattern of change with postnatal development. In adult animals, the highest levels of taurine were found in cardiac muscle. Pregnancy was associated with a fall in taurine concentration in all tissues, suggesting an influence of steroid hormones. As taurine is cotransported with Na+ in many systems it may be related to the increased water retention seen in pregnancy. It is concluded that marked changes in phosphoethanolamine and taurine levels occur during development and gestation, but that the changes are not interdependent, i.e., the changes are tissue specific.

Animals↗

The frog gonadotropin-releasing hormone-I (GnRH-I) gene has a mammalian-like expression pattern and conserved domains in GnRH-associated peptide, but brain onset is delayed until metamorphosis.

Recent evidence indicates a localized origin in the olfactory placode for the mammalian forebrain neurons that express GnRH. To identify the cellular and molecular signals that induce the GnRH phenotype, we cloned and characterized a cDNA encoding the GnRH prohormone, the precursor for both GnRH-I and GnRH-associated peptide in the frog, Xenopus laevis, an embryonic model accessible to experimental manipulation. The 396-base cDNA represented a single mRNA species encoding an 89-amino acid prepro-GnRH that, unlike a recently cloned fish GnRH gene, was identical to both the mammalian GnRH decapeptide as well as multiple domains within GnRH-associated peptide. Serial section in situ hybridization histochemistry and immunocytochemistry in adult frog localized a forebrain system comprising 250-350 cell bodies whose overall neuroanatomy, including fiber projections, was very similar to that described for mammals. However, neither Northern nor in situ hybridization detected GnRH expression in midbrain, arguing that another frog gene encodes the midbrain GnRH-II expression pattern described by many others using antisera directed against the fish GnRH-I or chicken GnRH-II decapeptides. In contrast to mammals and birds, in which GnRH-expressing cells migrate into embryonic forebrain, frog GnRH cells were first detected after they reached their final position in the preoptic area during the late larval period. Thus, although previous studies proposed a complex organization for the GnRH system in the frog, our findings show that similar to mammals, there is a single gene that can account for the continuum of GnRH-I cells spanning frog forebrain. However, unlike mammals, in frogs, for unknown reasons, GnRH-I gene expression is suppressed until metamorphic climax.

Amino Acid Sequence↗

Characterization of the suprachiasmatic nucleus in organotypic slice explant cultures.

Suprachiasmatic nuclei (SCN) from hypothalami of postnatal rats were maintained for 18-39 days in vitro as organotypic slice explants. Neuronal subtypes containing vasopressin (VP), vasoactive intestinal polypeptide (VIP), gastrin releasing hormone (GRP), and GABA were immunocytochemically identifiable in these cultures. In situ hybridization histochemistry was compatible with these SCN slice explant cultures, and mRNA encoding for VP was detected bilaterally within these nuclei. After 18 days in vitro, both VP mRNA and VP immunoreactivity increased from levels present on postnatal days 4 (the earliest age from which the explanted tissue was derived) to levels typical of adult SCNs. In contrast, the GRP expression remained low, characteristic of early postnatal animals and far lower than adult levels. This suggests that the developmental cues or programs necessary for enhanced VP expression are maintained in these cultures, while those affecting GRP expression are absent or inhibited. VIP-containing neurons were numerous in the cultures. Culture slices appeared healthy, and similar numbers and distributions of identifiable neurons within the SCN were observed, whether or not the slices were grown in the presence of serum. EM analysis revealed that the SCN in vitro is composed of tightly packed neurons, processes, and abundant synapses containing both clear and dense core vesicles, closely resembling the SCN in vivo. Vasopressinergic neuronal somata contained extensive Golgi systems and labeled secretory granules, the latter organelle being present also within processes and synaptic terminals. GABA-immunopositive processes and synaptic profiles were abundant, with labeling occurring particularly over secretory vesicles and mitochondria. This slice culture system effectively maintained much of the intrinsic organization and cellular components of the SCN for long periods in vitro and should be an excellent model system for studying the intrinsic molecular mechanisms and extrinsic cues which regulate neuronal phenotype in this circadian pacemaker.

Animals↗