http://www.sciencedirect.com/science/article/pii/S0197018616300250
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- The first report of the presence of autophagy in the human brain after stroke.
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- Observed the the increased appearance of autophagic vesicles after stroke in the human brain.
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- Observed an increase in staining in microtubule-associated protein 1 light chain 3 (LC3), sequestosome 1 (SQSTM1; also known as p62) in the human brain after stroke.
Abstract
Autophagy
is a homeostatic process for recycling proteins and organelles that is
increasingly being proposed as a therapeutic target for acute and
chronic neurodegenerative diseases, including stroke. Confirmation that
autophagy is present in the human brain after stroke is imperative
before prospective therapies can begin the translational process into
clinical trials. Our current study using human post-mortem tissue
observed an increase in staining in microtubule-associated protein 1
light chain 3 (LC3), sequestosome 1 (SQSTM1; also known as p62) and the
increased appearance of autophagic vesicles after stroke. These data
confirm that alterations in autophagy take place in the human brain
after stroke and suggest that targeting autophagic processes after
stroke may have clinical significance.
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