The Cytoskeletal Elements MAP2 and NF-L Show Substantial Alterations in Different Stroke Models While Elevated Serum Levels Highlight Especially MAP2 as a Sensitive Biomarker in Stroke Patients

Mol Neurobiol. 2021 Aug;58(8):4051-4069. doi: 10.1007/s12035-021-02372-3. Epub 2021 May 1.

Abstract

In the setting of ischemic stroke, the neurofilament subunit NF-L and the microtubule-associated protein MAP2 have proven to be exceptionally ischemia-sensitive elements of the neuronal cytoskeleton. Since alterations of the cytoskeleton have been linked to the transition from reversible to irreversible tissue damage, the present study investigates underlying time- and region-specific alterations of NF-L and MAP2 in different animal models of focal cerebral ischemia. Although NF-L is increasingly established as a clinical stroke biomarker, MAP2 serum measurements after stroke are still lacking. Therefore, the present study further compares serum levels of MAP2 with NF-L in stroke patients. In the applied animal models, MAP2-related immunofluorescence intensities were decreased in ischemic areas, whereas the abundance of NF-L degradation products accounted for an increase of NF-L-related immunofluorescence intensity. Accordingly, Western blot analyses of ischemic areas revealed decreased protein levels of both MAP2 and NF-L. The cytoskeletal alterations are further reflected at an ultrastructural level as indicated by a significant reduction of detectable neurofilaments in cortical axons of ischemia-affected areas. Moreover, atomic force microscopy measurements confirmed altered mechanical properties as indicated by a decreased elastic strength in ischemia-affected tissue. In addition to the results from the animal models, stroke patients exhibited significantly elevated serum levels of MAP2, which increased with infarct size, whereas serum levels of NF-L did not differ significantly. Thus, MAP2 appears to be a more sensitive stroke biomarker than NF-L, especially for early neuronal damage. This perspective is strengthened by the results from the animal models, showing MAP2-related alterations at earlier time points compared to NF-L. The profound ischemia-induced alterations further qualify both cytoskeletal elements as promising targets for neuroprotective therapies.

Keywords: Atomic force microscopy; Biomarker; Cerebral ischemia; MAP2; NF-L; Stroke.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Biomarkers / blood
  • Brain Ischemia / blood*
  • Brain Ischemia / diagnosis
  • Disease Models, Animal*
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microtubule-Associated Proteins / blood*
  • Middle Aged
  • Neurofilament Proteins / blood*
  • Prospective Studies
  • Rats
  • Rats, Wistar
  • Stroke / blood*
  • Stroke / diagnosis

Substances

  • Biomarkers
  • MAP2 protein, human
  • Microtubule-Associated Proteins
  • Neurofilament Proteins
  • neurofilament protein L