Behind the Wall-Compartment-Specific Neovascularisation during Post-Stroke Recovery in Mice

Cells. 2022 May 17;11(10):1659. doi: 10.3390/cells11101659.

Abstract

Ischemic stroke is a highly prevalent vascular disease leading to oxygen- and glucose deprivation in the brain. In response, ischemia-induced neovascularization occurs, which is supported by circulating CD34+ endothelial progenitor cells. Here, we used the transient middle cerebral artery occlusion (tMCAO) mouse model to characterize the spatio-temporal alterations within the ischemic core from the acute to the chronic phase using multiple-epitope-ligand cartography (MELC) for sequential immunohistochemistry. We found that around 14 days post-stroke, significant angiogenesis occurs in the ischemic core, as determined by the presence of CD31+/CD34+ double-positive endothelial cells. This neovascularization was accompanied by the recruitment of CD4+ T-cells and dendritic cells as well as IBA1+ and IBA1- microglia. Neighborhood analysis identified, besides pericytes only for T-cells and dendritic cells, a statistically significant distribution as direct neighbors of CD31+/CD34+ endothelial cells, suggesting a role for these cells in aiding angiogenesis. This process was distinct from neovascularization of the peri-infarct area as it was separated by a broad astroglial scar. At day 28 post-stroke, the scar had emerged towards the cortical periphery, which seems to give rise to a neuronal regeneration within the peri-infarct area. Meanwhile, the ischemic core has condensed to a highly vascularized subpial region adjacent to the leptomeningeal compartment. In conclusion, in the course of chronic post-stroke regeneration, the astroglial scar serves as a seal between two immunologically active compartments-the peri-infarct area and the ischemic core-which exhibit distinct processes of neovascularization as a central feature of post-stroke tissue remodeling. Based on our findings, we propose that neovascularization of the ischemic core comprises arteriogenesis as well as angiogenesis originating from the leptomenigeal vasculature.

Keywords: T-cell; angiogenesis; dendritic cell; microglia; multiplex immunohistochemistry; stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Ischemia* / pathology
  • Cicatrix / pathology
  • Endothelial Cells / pathology
  • Infarction, Middle Cerebral Artery / pathology
  • Mice
  • Neovascularization, Pathologic / pathology
  • Stroke* / complications
  • Stroke* / pathology

Grants and funding

This work was supported by the DFG grants SFB1039 (TP A08 and B08) SCHO817/3-3, GRK2336 (TP07), Cardio-Pulmonary Institute (CPI), EXC 2026, Project ID: 390649896 and the LOEWE initiative ACLF-I and the Fraunhofer Cluster of Excellence for Immune-Mediated Diseases (CIMD), Frankfurt/Main, Germany.