Abstract

The peri-infarct region, which surrounds the irreversible ischemic stroke area is named ischemic penumbra. This term emphasizes the borderline conditions for neurons placed within such a critical region. Area penumbra separates the ischemic core, where frank cell loss occurs, from the surrounding healthy brain tissue. Within such a brain region, nervous matter, and mostly neurons are impaired concerning metabolic conditions. The classic biochemical marker, which reliably marks area penumbra is the over-expression of the heat shock protein 70 (HSP70). However, other proteins related to cell clearing pathways are modified within area penumbra. Among these, autophagy proteins like LC3 increase in a way, which recapitulates Hsp70. In contrast, components, such as P20S, markedly decrease. Despite apparent discrepancies, the present study indicates remarkable overlapping between LC3 and P20S redistribution within area penumbra. In fact, the amount of both proteins is markedly reduced within vacuoles. Specifically, a massive loss of LC3 + P20S immuno-positive vacuoles (autophagoproteasomes) is reported here. This represents the most relevant sub-cellular alteration here described in cell clearing pathways within area penumbra. The functional significance of these findings remains to be determined and it will take a novel experimental stream to decipher the fine-tuning of such a phenomenon.

Highlights

  • Introduction iationsThe peri-infarct region, which surrounds the irreversible neuropathology following an ischemic stroke is named ischemic penumbra

  • heat shock protein 70 (HSP70) undergo an enlarged infarct followin the amount of LC3 and P20S is measured at different time intervals following ischemia

  • The decrease molecularentry mechanisms of HSP70 leaves open the chance of either or increased escapeare of each antigen known to counteract the deleterious effects produced by brain ischemia

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Summary

Results

Its rostro-caudal extent recruits the primary motor cortex Its rostro-caudal extent recruits the primary motor cortex (M1, in the legend of forelimb (S1FL, in the legend), dysgranular Ininfarct detail,area, the infarct area, whenbyevaluated by Nissl at 24 h occlusion corresponds a rostro-caudal from bregma to bregma. 3.28;to after MCA occlusiontocorresponds to aextent rostro-caudal extent+2.34 fromback bregma. At this size level, ofthe ischemia covers half of the brain. Dorso-ventral size of ischemia covers half of the brain. 4 of obtained image of electrocoagulation model of permanent focal ischemia following Blue Evans perfusion of a sham-operated mouse.

Representative
Nissl staining of representative mouse brain
12. Ultrastructural
The Amount and Compartmentalization
The Amount and Compartmentalization of P20S within Area Penumbra
Permanent Focal Ischemia in Mice
Tissue Preparation
Histology
Immune-Histochemical Analysis
SDS Page Immunoblotting
Post-Embedding Immuno-Gold Microscopy
Statistical Analyses

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