4.6 Article

Molecular and Cellular Analysis of the Repair of Zebrafish Optic Tectum Meninges Following Laser Injury

Journal

CELLS
Volume 11, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/cells11132016

Keywords

fish; midbrain; meninx; meningioma; arachnoid space; two-photon laser injury; ischemic accident; brain mild traumatic injury; radar plots; water channels; solute carriers

Categories

Funding

  1. Leducq Foundation
  2. ANR-TEFOR-'Investissement davenir' [ANR-II-INBS-0014]
  3. ANR FEATS [ANR-19CE34-0005]
  4. ANR NewBornNeurons [ANR-21-CE16-0038]
  5. CNRS
  6. INRAE
  7. l'Agence Nationale de la Recherche [ANR-11-EQPX-0029, ANR-10-INBS-04, ANR-11-IDEX-0003-02]
  8. France Genomique - French National Program Investissement d'Avenir [ANR-10-INBS-09]
  9. Agence Nationale de la Recherche (ANR) [ANR-21-CE16-0038] Funding Source: Agence Nationale de la Recherche (ANR)

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In this study, the recruitment of cells following optic tectum (OT) injury in zebrafish was investigated. The results showed that deep-laser injury did not induce massive recruitment of cells, while surface-laser injury led to the migration of different cell types to the injury site. This study provides important insights into the mechanisms of meninges repair in zebrafish and potentially in mammalian meninges.
We studied cell recruitment following optic tectum (OT) injury in zebrafish (Danio rerio), which has a remarkable ability to regenerate many of its organs, including the brain. The OT is the largest dorsal layered structure in the zebrafish brain. In juveniles, it is an ideal structure for imaging and dissection. We investigated the recruited cells within the juvenile OT during regeneration in a Pdgfr beta-Gal4:UAS-EGFP line in which pericytes, vascular, circulating, and meningeal cells are labeled, together with neurons and progenitors. We first performed high-resolution confocal microscopy and single-cell RNA-sequencing (scRNAseq) on EGFP-positive cells. We then tested three types of injury with very different outcomes (needle (mean depth in the OT of 200 mu m); deep-laser (depth: 100 to 200 mu m depth); surface-laser (depth: 0 to 100 mu m)). Laser had the additional advantage of better mimicking of ischemic cerebral accidents. No massive recruitment of EGFP-positive cells was observed following laser injury deep in the OT. This type of injury does not perturb the meninx/brain-blood barrier (BBB). We also performed laser injuries at the surface of the OT, which in contrast create a breach in the meninges. Surprisingly, one day after such injury, we observed the migration to the injury site of various EGFP-positive cell types at the surface of the OT. The migrating cells included midline roof cells, which activated the PI3K-AKT pathway; fibroblast-like cells expressing numerous collagen genes and most prominently in 3D imaging; and a large number of arachnoid cells that probably migrate to the injury site through the activation of cilia motility genes, most likely being direct targets of the FOXJ1a gene. This study, combining high-content imaging and scRNAseq in physiological and pathological conditions, sheds light on meninges repair mechanisms in zebrafish that probably also operate in mammalian meninges.

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