Analysis of the brain mural cell transcriptome

Autor: Annika Keller, Maarja Andaloussi Mäe, Thibaud Lebouvier, Bongnam Jung, Elisabeth Raschperger, Jennifer J. Hofmann, Liqun He, Michael Vanlandewijck, Koji Ando, Christer Betsholtz
Přispěvatelé: University of Zurich, Betsholtz, Christer
Jazyk: angličtina
Rok vydání: 2016
Předmět:
0301 basic medicine
In silico
Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology)
Molecular Biology
Microbiology
Biochemistry or Biopharmacy)

610 Medicine & health
In situ hybridization
Biology
Mural cell
Article
Transcriptome
03 medical and health sciences
Mice
10180 Clinic for Neurosurgery
medicine
Animals
Cardiac and Cardiovascular Systems
Gene
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi)
molekylärbiologi
mikrobiologi
biokemi eller biofarmaci)

1000 Multidisciplinary
Multidisciplinary
Kardiologi
Staining and Labeling
Sequence Analysis
RNA

Gene Expression Profiling
Brain
Cell sorting
Flow Cytometry
Cell biology
Gene expression profiling
030104 developmental biology
medicine.anatomical_structure
Microvessels
Pericyte
Pericytes
Zdroj: Scientific Reports
Popis: Pericytes, the mural cells of blood microvessels, regulate microvascular development and function and have been implicated in many brain diseases. However, due to a paucity of defining markers, pericyte identification and functional characterization remain ambiguous and data interpretation problematic. In mice carrying two transgenic reporters, Pdgfrb-eGFP and NG2-DsRed, we found that double-positive cells were vascular mural cells, while the single reporters marked additional, but non-overlapping, neuroglial cells. Double-positive cells were isolated by fluorescence-activated cell sorting (FACS) and analyzed by RNA sequencing. To reveal defining patterns of mural cell transcripts, we compared the RNA sequencing data with data from four previously published studies. The meta-analysis provided a conservative catalogue of 260 brain mural cell-enriched gene transcripts. We validated pericyte-specific expression of two novel markers, vitronectin (Vtn) and interferon-induced transmembrane protein 1 (Ifitm1), using fluorescent in situ hybridization and immunohistochemistry. We further analyzed signaling pathways and interaction networks of the pericyte-enriched genes in silico. This work provides novel insight into the molecular composition of brain mural cells. The reported gene catalogue facilitates identification of brain pericytes by providing numerous new candidate marker genes and is a rich source for new hypotheses for future studies of brain mural cell physiology and pathophysiology.
Databáze: OpenAIRE