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Biomedical subjects

D Richter

Publications and source records attributed to D Richter.

At least 325 records · Page 18Linked to original sources
PubMed1986

Brattleboro rat hypothalamic neurons transcribe vasopressin gene: evidence from in situ hybridization.

In situ hybridization has been used to identify specific hypothalamic magnocellular neurons, in normal and Brattleboro rats, that contain vasopressin (VP) or oxytocin (OT) mRNA. The subnuclear distribution of identified neurons in hypothalamic magnocellular nuclei after hybridization with several probes specific for OT or VP mRNA was in direct agreement with immunocytochemical descriptions of the distribution of cells containing VP or OT hormone. The number of grains per cell suggested that Brattleboro rats contained greater levels of OT mRNA, while hybridization with VP probes produced fewer grains in tissue from Brattleboro rats compared to normal rats. This paper provides the first cell-by-cell description of VP gene expression in the Brattleboro rat and demonstrates that VP gene transcription is confined precisely to the magnocellular neurons that normally synthesize VP hormone in normal rats.

Animals↗
PubMed1986

In situ hybridization technique to localize rRNA and mRNA in mammalian neurons.

In situ hybridization provides a method for identifying cells that contain specific nucleic acid sequences. This report outlines an in situ hybridization procedure for mammalian neural tissue. The method maintains morphological quality and produces excellent specificity. Seven tritiated nucleic acid probes were examined: two ribosomal RNA probes, a control pBR322 plasmid probe, two probes encoding portions of the gene for oxytocin, one probe each encoding a portion of vasopressin glycoprotein, and neurophysin. Using cryostat-cut rat brain sections, rRNA probes labeled the cytoplasm of all cells and the nucleoli of larger neurons. The plasmid probe failed to produce a strong signal. Oxytocin and vasopressin probes appropriately labeled the cytoplasm of hypothalamic magnocellular neurons. Vasopressin parvocellular neurons were not identified by the current method, and the shorter length neurophysin probe failed to produce a signal. Methodological variables were examined by counting autoradiographic grains in cells. The longer oxytocin probe produced a stronger signal than the shorter oxytocin and vasopressin probes, and higher probe concentrations resulted in stronger signal. Hybridization could be abolished by tissue pretreatment with RNAse A, and longer exposure time increased signal strength. The outlined fixation steps with fresh-frozen tissue produced a superior signal compared to paraformaldehyde-perfused tissue.

Animals↗
PubMed1986

The neurohypophyseal hormones vasopressin and oxytocin. Precursor structure, synthesis and regulation.

Complete cDNA sequences for the vasopressin and oxytocin precursor polyproteins have been determined for the rat, calf, human and pig (vasopressin only), indicating the essential conservation of the precursor structures throughout mammals. DNA probes specific for vasopressin or oxytocin mRNAs have been used to identify both classic (hypothalamic) and novel (thymus, corpus luteum, phaeochromocytoma) sites of hormone expression. Semiquantitative DNA/RNA hybridization suggests that in rats expression of the vasopressin and oxytocin genes is positively effected by osmotic stress, negatively by a systemically applied excess of vasopressin; in the latter experiment a reduction in the hypothalamic levels of vasopressin and oxytocin mRNAs in normal and Brattleboro rats have been observed. This suggests a feedback regulation by the hormone as a possible element in controlling the transcription of the vasopressin gene.

Animals↗
PubMed1985

Expression of the vasopressin and oxytocin genes in human hypothalami.

Poly(A)+ RNA isolated from post-mortem human hypothalami has been used to characterize the poly-protein precursors to vasopressin and oxytocin. Translation in a cell-free system and subsequent immuno-precipitation with antibodies raised against either vasopressin or neurophysin identified a product of Mr 19000 (prepro-vasopressin). A second less intense product of Mr 16500 was tentatively identified as prepro-oxytocin. A cDNA library derived from the human hypothalamic poly(A)+ RNA was screened for vasopressin and oxytocin-encoding cDNA using heterologous probes; clones encoding the two precursors were identified and found to be organized as their rat and bovine counterparts. Northern blot analysis shows that the mRNAs for the two prepro-hormones consist of approximately 840 (AVP) and approximately 700 (OT) nucleotides.

Base Sequence↗
PubMed1985

Morphology of physiologically identified slowly adapting lung stretch receptor afferents stained with intra-axonal horseradish peroxidase in the nucleus of the tractus solitarius of the cat. I. A light microscopic analysis.

The present series of experiments was designed to study the organization of preterminal processes and synaptic boutons of single physiologically identified slowly adapting receptor (SAR) pulmonary stretch afferent fibers. Intra-axonally injected horseradish peroxidase-wheat germ agglutinin (HRP-WGA) conjugate was used as the label. In the first paper, we describe the pattern of arborization of axon collaterals from single physiologically identified SAR afferent fibers evident in the various subnuclei of the nucleus of the tractus solitarius (nTS). In the second paper, details are presented regarding the ultrastructure of these synaptic boutons and axon collaterals. A number of significant findings resulted from this study: (1) A single lung stretch SAR afferent fiber arborized over a considerable distance rostrocaudally in the brain stem (1,700-2,100 microns). (2) A single lung stretch SAR afferent fiber terminated as hundreds of bouton terminals (650-1,180). (3) There was a remarkable consistency in the subnuclei of the nTS that received these terminal arborizations of SAR afferents. (4) The ventral (vnTS), intermediate (nI), ventrolateral (vlnTS), and interstitial (ni) subnuclei of the nTS were the only regions of the nTS receiving bouton terminals of SAR afferent fibers. (5) Under the light microscope the pattern of termination of SAR afferents was similar in all the axons studied in this series. (6) The injected parent axon in each case could be followed in the TS at all levels and remained consistent with regard to position and orientation and could be traced rostrally to levels as far as 3.5 mm rostral to the obex whereas the region of terminal arborization was located around 1.7-2.1 mm rostral to the obex. This pattern indicates that a single lung stretch SAR afferent fiber descends caudally upon entering the nTS. In the cat vagal afferent fibers are known to enter the medulla at levels between 0.5 mm and 3.2 mm rostral to the obex (Kalia and Mesulam, '80a). The results of the light microscopic analysis presented in this article indicate that lung stretch (SAR) afferents from the lungs and tracheobronchial tree have distinctly localized patterns of distribution in the nTS. In addition, these findings support the concept that representation of pulmonary afferents in the medulla is constituted by a differentiated distribution of nerve terminals in the various subnuclei of the nTS. Modality-specific localization (SAR afferents in this case) appears to be predominant in the nTS. The widespread rostrocaudal distribution of the terminal field of a single lung stretch SAR afferent is remarkable.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗
PubMed1985

Morphology of physiologically identified slowly adapting lung stretch receptor afferents stained with intra-axonal horseradish peroxidase in the nucleus of the tractus solitarius of the cat. II. An ultrastructural analysis.

The nucleus of the tractus solitarius is a site for termination of primary afferents originating from a variety of visceral receptors. The localization of bouton terminals of slowly adapting lung stretch (SAR) afferent fibers originating from the tracheobronchial tree have been described in the companion paper (Kalia and Richter, '85). The most conspicuous finding regarding the location of SAR terminals is that they are concentrated within specific subnuclear groups of the nucleus of the tractus solitarius (nTS) and are distributed widely in the rostrocaudal plane of the medulla oblongata. These light microscopic features have provided us with valuable information with regard to the organization of visceral afferents in the central nervous system. The synaptic profiles formed by the 476 bouton terminals of these HRP-labeled afferents have been described in this paper in serial thin sections. All of the bouton terminals examined under the electron microscope were found to contain round synaptic vesicles. Synaptic boutons (1.0-3.0 microns in diameter) were usually of the en passant variety and made contact with different structures depending upon the subnucleus which was examined. In the ventral (v) and the ventrolateral (vl) subnuclei of the nTS, asymmetrical (type I) synaptic contacts containing round, clear synaptic vesicles of 35-50 microns in diameter were found and these contacts were made with (1) the soma of cell bodies located in that subnucleus; (2) spiny dendrites in that nucleus; (3) vesicle-containing axon terminals that were presynaptic to the HRP-labeled bouton terminal; and (4) vesicle-containing dendrites in which the HRP profile was presynaptically located. The terminal axon remained myelinated till the last 1 micron before the bouton terminal was formed. There was no distinct, unmyelinated portion of the terminal axon. The synaptic bouton received axon-axonal synapses from unlabeled bouton terminals containing round, clear vesicles. This is the first report of the localization of these afferent fibers as well as of the regional variations in the ultrastructure of boutons of physiologically identified terminals. It appears likely that the lung stretch afferent fibers, by having axon-axonal as well as axon-somatic contact in the ventral, ventrolateral, and intermediate subnuclei of the nTS, can interact in a variety of different ways in this region. The significance of these features in relation to the precise influence of respiratory afferents on central respiratory mechanisms needs to be evaluated further.

Afferent Pathways↗
PubMed1985

Ovulation triggers oxytocin gene expression in the bovine ovary.

The gene for the nonapeptide neurohormone oxytocin is highly expressed in the bovine corpus luteum. Measurements of oxytocin-specific mRNA through the oestrous cycle of non-pregnant cows show that transcription is maximal accompanying ovulation and decreases rapidly thereafter. In contrast, immunohistochemistry shows neurophysin peptide levels to be greatest at mid-cycle. Low levels of oxytocin mRNA are detected in follicles and in the luteolytic half of the cycle. This mRNA is virtually absent in the corpus luteum of pregnant cattle. No cyclicity is evident in hypothalamic oxytocin mRNA levels.

Animals↗
PubMed1985

Verapamil in primary pulmonary hypertension.

An 8 year old girl with primary pulmonary hypertension and signs of heart failure was given 17.5 mg of verapamil injected into the pulmonary artery over 25 minutes to test for the reversibility of pulmonary arteriolar obstruction. Pulmonary artery pressure fell from 70/50 to 35/25 mm Hg. Treatment with 40 mg verapamil by mouth four times daily was started, and she was discharged. She gradually became asymptomatic and resumed the activities of a normal child of school age. On recatheterisation seven months later her pulmonary artery pressure was 30/10 mm Hg. She was still doing well 12 months after the start of treatment.

Blood Pressure↗
PubMed1984

The mutant vasopressin gene from diabetes insipidus (Brattleboro) rats is transcribed but the message is not efficiently translated.

The vasopressin gene from normal and diabetes insipidus (Brattleboro) rats has been isolated and sequenced. Except for a single deletion of a G residue in region coding for the neurophysin carrier protein the approximately 2300 nucleotides of both genes are identical. Blot analysis of hypothalamic RNA as well as transfection and microinjection experiments indicate that the mutant gene is correctly transcribed and spliced, however the resulting mRNA is not efficiently translated.

Animals↗
PubMed1984

[Epithelioid sarcoma. Apropos of 3 cases].

The authors present two cases of epithelioid sarcoma of the hand and one of the foot with clinical interest. This recently described tumor (Enzinger, 1970), is relatively rare. It occurs in the hand, forearm, pretibial region and foot and affects principally young adults. It should be emphasized, and this is borne out in the literature, that this tumor may appear perfectly benign and often has a course of long duration. The difficulty of clinical and especially of histologic diagnosis as well as the difficulty of determining the boundaries of extension of the tumor make it necessary to carry out radical surgery (amputation or rarely block excision). Every author agrees that local excision is to be condemned, there being an 85% recurrence rate. Spread of the tumor is by way of the fascial planes and tendon sheaths. Lymphatic and pulmonary metastases occur particularly when there is vascular invasion.

Adult↗
PubMed1984

Cell-free synthesized precursor to somatostatin-28 from the rat hypothalamus.

Cell-free translation of rat hypothalamic mRNA and specific immunoprecipitation were used to identify a polypeptide of 16,000 apparent molecular weight as prepro-somatostatin. Quantifying these results suggested that the somatostatin-specific mRNA represented less than 0.01% of the total hypothalamic mRNA. Co-translational addition of microsomal membranes led to the in vitro synthesis of a pro-form of 14,500 molecular weight. By using antisera specifically recognizing 3 different but overlapping segments of somatostatin-28 (SRIF-28), the rat prepro-somatostatin was shown to contain antigenic determinants of this N-terminally extended somatostatin as well as of the tetradecapeptide (SRIF-14). Sequential immunoprecipitation experiments implied the existence of only a single somatostatin precursor among the rat hypothalamic translation products, which would have to be differentially processed to allow release of both SRIF-28 and SRIF-14.

Animals↗
PubMed1984

The gene for the hypothalamic peptide hormone oxytocin is highly expressed in the bovine corpus luteum: biosynthesis, structure and sequence analysis.

Expression of the vasopressin and oxytocin genes has been described so far only in the hypothalamus. We report here that at least the oxytocin gene is highly transcribed in the bovine corpus luteum during the mid-luteal phase of the oestrous cycle. Luteal cDNA sequence analysis as well as cell-free translation studies showed that the luteal mRNA is essentially similar to that in the hypothalamus, except that in the corpus luteum the poly(A) tail of this mRNA is shorter. When calculating the relative amounts per organ, the active corpus luteum produces approximately 250 times more oxytocin mRNA than a single hypothalamus.

Amino Acid Sequence↗
PubMed1984

Subcellular distribution of ribosomal proteins S6 and eL12. Analysis by autoradiography and immunofluorescence of sections from oocytes of Xenopus laevis.

The process of ribosome assembly in eukaryotes was studied by injecting tritium-labeled ribosomal proteins S6 and eL12 into oocytes of Xenopus laevis. The subcellular distribution of the two proteins was visualized by means of autoradiography in sections of oocytes. Protein S6 but not eL12 was found in the nucleus where it accumulated at the nucleoli. In the presence of actinomycin D the accumulation of S6 at the nucleoli was reduced. In-situ immunofluorescence studies indicated that S6 is located at the nucleoli and eL12 exclusively in the cytoplasm. It appears that S6 is involved in the early ribosomal assembly process at the nucleoli, whereas eL12 is restricted to the cytoplasm where it is incorporated into 60S ribosomal subunits in a late assembly step.

Animals↗
PubMed1984

Process surveillance: auditing infection control policies and procedures.

The infection control team in a university hospital designed, implemented, and evaluated a program to audit infection control policies. Process surveillance techniques of observation and monitoring were used during surveys of patient care areas to evaluate infection control practices. Nineteen unit surveys have been completed in a 2-year period. Analysis of the program has demonstrated it to be an effective method to determine compliance with infection control policies.

Communicable Disease Control↗
PubMed1984

Structure and comparison of the oxytocin and vasopressin genes from rat.

The gene encoding the precursor protein to the hormone oxytocin and its associated neurophysin has been isolated from a rat genomic library, and its sequence has been determined. The small gene (approximately equal to 850 base pairs) predicts a mRNA of approximately equal to 500 bases [without the poly(A) tail]. The exon-intron organization is similar to that of the vasopressin gene, with two splice sites in the protein-coding region. The first exon (A) comprises the 5' noncoding promoter region, a putative signal peptide, the nonapeptide hormone oxytocin, and the NH2-terminal, variable region of neurophysin. The second exon (B) encodes the central, conserved region of neurophysin, and the third exon (C) encodes the remaining COOH terminus of neurophysin, with an additional arginine residue at its end, presumably cleaved off during post-translational processing. A stretch of 143 nucleotides within exon B, except for a single base change, is entirely homologous to the equivalent part of the rat vasopressin gene, offering support for a gene conversion event having recently affected the two genes.

Animals↗