4 research outputs found
<i>SEMA3A</i> mutations identified in Kallmann syndrome patients.
<p><i>SEMA3A</i> mutations identified in Kallmann syndrome patients.</p
Expression of the Sema3A coreceptor Nrp1 by vomeronasal/terminal nerve fibers and migrating GnRH cells in human and mouse embryos.
<p>(A) Schematic representation of the head of a mouse embryo at E14.5, showing the scaffold of vomeronasal/terminal nerve fibers (in red) along which GnRH cells (in blue) migrate from the nose to the ventral forebrain region. Several areas along this migratory path have been shown to produce Sema3A, including the frontonasal mesenchyme and the olfactory bulb region <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002896#pgen.1002896-Schwarting1" target="_blank">[21]</a>, <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002896#pgen.1002896-Giger1" target="_blank">[33]</a>. Boxes indicate the locations of the sagittal sections shown in (B) and (C). Abbreviations: oe, olfactory epithelium; vno, vomeronasal organ; nm, frontonasal mesenchyme; mob, main olfactory bulb; aob, accessory olfactory bulb; vfb, ventral forebrain; 3V, third ventricle. (B) Sagittal section of the frontonasal region in an E14.5 mouse embryo. In the frontonasal mesenchyme (nm), migrating GnRH-immunoreactive cells (green) are morphologically associated with Nrp1-immunoreactive nerve fibers (red) originating in the vomeronasal organ (vno). Single plane confocal images at higher magnification (insets) show that GnRH cells are Nrp1-immunoreactive (green+red = yellow staining). (C) Sagittal section of the ventral forebrain (vfb) in an E14.5 mouse embryo. The peripherin-immunoreactive (green) fibers of the caudal branch of the vomeronasal nerve (arrows) are also Nrp1-immunoreactive (red), as shown by their yellow staining (green+red). (D) Sagittal section of the olfactory epithelium (oe) and olfactory bulb (ob) regions (left panel) and detail of the frontonasal region (right panel) in a 9 week-old human fetus. Clusters of GnRH-immunoreactive cells (green, arrowheads) are visible in the frontonasal mesenchyme (nm) and the rostral forebrain (fb). In the frontonasal region, these cells migrate in close contact with Nrp1-immunoreactive axons (red). Note that migrating GnRH cells are also Nrp1-immunoreactive, as shown by their yellow staining (green+red) in the right panel (arrows). Scale bars: 100 µm (25 µm in insets).</p
Defects in olfactory and vomeronasal axons, and GnRH cell migration in <i>Nrp1</i><sup>sema/sema</sup> mutant mice.
<p>(A) Coronal sections of the right olfactory epithelium (oe) and olfactory bulb (ob) regions (left panels), and detail of the olfactory bulb showing the olfactory nerve layer (nl) and glomerular layer (gl) (right panels) in <i>Nrp1</i><sup>+/+</sup> and <i>Nrp1</i><sup>sema/sema</sup> newborn (P0) mice. Axons of the olfactory receptor neurons were immunostained (red) using an antibody directed against the olfactory marker protein (OMP). In the <i>Nrp1</i><sup>sema/sema</sup> mouse, the immunostaining is both enlarged below the olfactory bulb ventro-medial aspect (asterisks) and markedly reduced in the glomerular layer (arrowheads) compared to wild-type. (B) Sagittal sections of the rostral and ventral forebrain regions (left panels), and detail of the caudal branch of the vomeronasal nerve (right panels) in <i>Nrp1</i><sup>+/+</sup> and <i>Nrp1</i><sup>sema/sema</sup> E14.5 mouse embryos. A crystal of the DiI lipophilic fluorescent dye has been placed in the vomeronasal organ lumen to anterogradely label vomeronasal axons. The vomeronasal nerve extends across the medial aspect of the olfactory bulb and projects both dorsally, to the accessory olfactory bulb, and caudally, to the ventral forebrain (vfb). In the mutant mouse, fibers in the caudal branch are scarce compared to wild-type. (C) Sagittal sections of the rostral and ventral forebrain regions at E14.5, immunostained for GnRH (green). Note the abnormal distribution of GnRH-immunoreactive cells in the <i>Nrp1</i><sup>sema/sema</sup> mouse (arrows). (D) Coronal sections of the preoptic region (upper panels) showing GnRH neuroendocrine cells (green) and their projections in the median eminence (me, arrows) (lower panels) in <i>Nrp1</i><sup>+/+</sup> and <i>Nrp1</i><sup>sema/sema</sup> newborn (P0) mice. The immunostaining is reduced in the <i>Nrp1</i><sup>sema/sema</sup> mouse. (E) Quantitative analysis (mean ± s.d.) of GnRH cell distributions in <i>Nrp1</i><sup>+/+</sup> and <i>Nrp1</i><sup>sema/sema</sup> mice at E14.5 and P0. * and ** denote statistically significant differences between genotypes in the indicated head regions (two-way ANOVA followed by Tukey's range test) with <i>p</i><0.05 and <i>p</i><0.01, respectively. Note that the total numbers of GnRH cells are not statistically different between <i>Nrp1</i><sup>+/+</sup> and <i>Nrp1</i><sup>sema/sema</sup> mice at E14.5 or P0 (Student's t-test, <i>p</i>>0.05). Other abbreviations: cx, cerebral cortex; ovlt, organum vasculosum of lamina terminalis; 3v, third ventricle. Scale bars: 100 µm (50 µm in inset).</p
Additional file 1: of Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case–control study
The questionnaire used in the current study. (PDF 620 kb