4.6 Article

Enteric Glia Express Proteolipid Protein 1 and Are a Transcriptionally Unique Population of Glia in the Mammalian Nervous System

Journal

GLIA
Volume 63, Issue 11, Pages 2040-2057

Publisher

WILEY
DOI: 10.1002/glia.22876

Keywords

enteric nervous system; neuroglia; RNA-Seq; gastrointestinal tract

Categories

Funding

  1. NIDDK [F32DK098903]
  2. NASPGHAN
  3. George Ferry Young Investigator Award
  4. NINDS [R01 NS35884]
  5. NICHD [P30-HD18655]
  6. NSF
  7. Milton Fund
  8. Divisions of Pediatric Gastroenterology, Hepatology, and Nutrition at Boston Children's Hospital
  9. Columbia University Medical Center

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In the enteric nervous system (ENS), glia outnumber neurons by 4-fold and form an extensive network throughout the gastrointestinal tract. Growing evidence for the essential role of enteric glia in bowel function makes it imperative to understand better their molecular marker expression and how they relate to glia in the rest of the nervous system. We analyzed expression of markers of astrocytes and oligodendrocytes in the ENS and found, unexpectedly, that proteolipid protein 1 (PLP1) is specifically expressed by glia in adult mouse intestine. PLP1 and S100 beta are the markers most widely expressed by enteric glia, while glial fibrillary acidic protein expression is more restricted. Marker expression in addition to cellular location and morphology distinguishes a specific subpopulation of intramuscular enteric glia, suggesting that a combinatorial code of molecular markers can be used to identify distinct subtypes. To assess the similarity between enteric and extraenteric glia, we performed RNA sequencing analysis on PLP1-expressing cells in the mouse intestine and compared their gene expression pattern to that of other types of glia. This analysis shows that enteric glia are transcriptionally unique and distinct from other cell types in the nervous system. Enteric glia express many genes characteristic of the myelinating glia, Schwann cells and oligodendrocytes, although there is no evidence of myelination in the murine ENS.

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