Characterization, isolation, and in vitro culture of leptomeningeal fibroblasts

J Neuroimmunol. 2021 Dec 15:361:577727. doi: 10.1016/j.jneuroim.2021.577727. Epub 2021 Sep 29.

Abstract

Meninges, or the membranous coverings of the brain and spinal cord, play host to dozens of morbid pathologies. In this study we provide a method to isolate the leptomeningeal cell layer, identify leptomeninges in histologic slides, and maintain leptomeningeal fibroblasts in in vitro culture. Using an array of transcriptomic, histological, and cytometric analyses, we identified ICAM1 and SLC38A2 as two novel markers of leptomeningeal cells in vivo and in vitro. Our results confirm the fibroblastoid nature of leptomeningeal cells and their ability to form a sheet-like layer that covers the brain and spine parenchyma. These findings will enable researchers in central nervous system barriers to describe leptomeningeal cell functions in health and disease.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Aged
  • Amino Acid Transport System A / analysis
  • Amino Acid Transport System A / biosynthesis
  • Amino Acid Transport System A / genetics
  • Animals
  • Base Sequence
  • Biomarkers
  • Cell Separation
  • Cells, Cultured
  • Child, Preschool
  • Female
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Humans
  • Intercellular Adhesion Molecule-1 / analysis
  • Intercellular Adhesion Molecule-1 / biosynthesis
  • Intercellular Adhesion Molecule-1 / genetics
  • Male
  • Meninges / cytology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microdissection
  • Middle Aged
  • Primary Cell Culture
  • Staining and Labeling / methods
  • Transcriptome

Substances

  • Amino Acid Transport System A
  • Biomarkers
  • ICAM1 protein, human
  • Icam1 protein, mouse
  • SLC38A2 protein, human
  • Slc38a2 protein, mouse
  • Intercellular Adhesion Molecule-1