6533b824fe1ef96bd1280140

RESEARCH PRODUCT

Bi- and uniciliated ependymal cells define continuous floor-plate-derived tanycytic territories

José Manuel García-verdugoChristian OrtizZaman MirzadehBin ChenSara Gil-perotinNader SanaiYael KusneMaria Duran-morenoArturo Alvarez-buyllaElaine Cabrales

subject

Male0301 basic medicineEpendymal CellScienceEpendymoglial CellsGene ExpressionGeneral Physics and AstronomyMice TransgenicS100 Calcium Binding Protein beta SubunitFourth ventricleArticleGeneral Biochemistry Genetics and Molecular BiologyNestinMice03 medical and health sciencesLateral ventriclesEpendymaGlial Fibrillary Acidic ProteinmedicineAnimalsHumansVimentinCell LineageHedgehog ProteinsCiliaSonic hedgehogAgedBrain VentricleFloor plateBrain MappingMultidisciplinaryThird ventriclebiologyQCD24 AntigenCell DifferentiationGeneral ChemistryAnatomyMiddle Aged030104 developmental biologymedicine.anatomical_structureCell Trackingbiology.proteinFemaleNerve NetEpendymaBiomarkers

description

Multiciliated ependymal (E1) cells line the brain ventricles and are essential for brain homeostasis. We previously identified in the lateral ventricles a rare ependymal subpopulation (E2) with only two cilia and unique basal bodies. Here we show that E2 cells form a distinct biciliated epithelium extending along the ventral third into the fourth ventricle. In the third ventricle floor, apical profiles with only primary cilia define an additional uniciliated (E3) epithelium. E2 and E3 cells' ultrastructure, marker expression and basal processes indicate that they correspond to subtypes of tanycytes. Using sonic hedgehog lineage tracing, we show that the third and fourth ventricle E2 and E3 epithelia originate from the anterior floor plate. E2 and E3 cells complete their differentiation 2–3 weeks after birth, suggesting a link to postnatal maturation. These data reveal discrete bands of E2 and E3 cells that may relay information from the CSF to underlying neural circuits along the ventral midline.

https://doi.org/10.1038/ncomms13759