Impairment of spinal CSF flow precedes immune cell infiltration in an active EAE model

J Neuroinflammation. 2024 Oct 23;21(1):272. doi: 10.1186/s12974-024-03247-9.

Abstract

Accumulation of immune cells and proteins in the subarachnoid space (SAS) is found during multiple sclerosis and in the animal model experimental autoimmune encephalomyelitis (EAE). Whether the flow of cerebrospinal fluid (CSF) along the SAS of the spinal cord is impacted is yet unknown. Combining intravital near-infrared (NIR) imaging with histopathological analyses, we observed a significantly impaired bulk flow of CSF tracers within the SAS of the spinal cord prior to EAE onset, which persisted until peak stage and was only partially recovered during chronic disease. The impairment of spinal CSF flow coincided with the appearance of fibrin aggregates in the SAS, however, it preceded immune cell infiltration and breakdown of the glia limitans superficialis. Conversely, cranial CSF efflux to cervical lymph nodes was not altered during the disease course. Our study highlights an early and persistent impairment of spinal CSF flow and suggests it as a sensitive imaging biomarker for pathological changes within the leptomeninges.

Keywords: CSF flow; Cerebrospinal fluid; Experimental autoimmune encephalomyelitis; Glia limitans; Multiple sclerosis; Neuroinflammation; Subarachnoid space.

MeSH terms

  • Animals
  • Cerebrospinal Fluid* / immunology
  • Disease Models, Animal
  • Encephalomyelitis, Autoimmune, Experimental* / cerebrospinal fluid
  • Encephalomyelitis, Autoimmune, Experimental* / immunology
  • Encephalomyelitis, Autoimmune, Experimental* / pathology
  • Female
  • Mice
  • Mice, Inbred C57BL*
  • Myelin-Oligodendrocyte Glycoprotein / immunology
  • Spinal Cord* / immunology
  • Spinal Cord* / pathology
  • Subarachnoid Space / pathology

Substances

  • Myelin-Oligodendrocyte Glycoprotein