| Literature DB >> 32295886 |
Jolien Wolbert1, Xiaolin Li1, Michael Heming1, Anne K Mausberg2, Dagmar Akkermann3, Clara Frydrychowicz3, Robert Fledrich4, Linda Groeneweg5, Christian Schulz6, Mark Stettner2, Noelia Alonso Gonzalez5, Heinz Wiendl1, Ruth Stassart3, Gerd Meyer Zu Hörste7.
Abstract
Peripheral nerves contain axons and their enwrapping glia cells named Schwann cells (SCs) that are either myelinating (mySCs) or nonmyelinating (nmSCs). Our understanding of other cells in the peripheral nervous system (PNS) remains limited. Here, we provide an unbiased single cell transcriptomic characterization of the nondiseased rodent PNS. We identified and independently confirmed markers of previously underappreciated nmSCs and nerve-associated fibroblasts. We also found and characterized two distinct populations of nerve-resident homeostatic myeloid cells that transcriptionally differed from central nervous system microglia. In a model of chronic autoimmune neuritis, homeostatic myeloid cells were outnumbered by infiltrating lymphocytes which modulated the local cell-cell interactome and induced a specific transcriptional response in glia cells. This response was partially shared between the peripheral and central nervous system glia, indicating common immunological features across different parts of the nervous system. Our study thus identifies subtypes and cell-type markers of PNS cells and a partially conserved autoimmunity module induced in glia cells.Entities:
Keywords: Schwann cell; peripheral nervous system; single cell RNA-seq; transcriptomics
Year: 2020 PMID: 32295886 DOI: 10.1073/pnas.1912139117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205