Alpha synuclein is transported into and out of the brain by the blood–brain barrier

•Alpha-synuclein crosses the blood–brain barrier in both the blood-to-brain and the brain-to-blood direction.•Inflammation as induced by lipopolysaccharide increases alpha-synuclein entry into brain, probably because of BBB disruption. Alpha-synuclein (α-Syn), a small protein with multiple physiolog...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2014-12, Vol.62, p.197-202
Hauptverfasser: Sui, Yu-Ting, Bullock, Kristin M., Erickson, Michelle A., Zhang, Jing, Banks, W.A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Alpha-synuclein crosses the blood–brain barrier in both the blood-to-brain and the brain-to-blood direction.•Inflammation as induced by lipopolysaccharide increases alpha-synuclein entry into brain, probably because of BBB disruption. Alpha-synuclein (α-Syn), a small protein with multiple physiological and pathological functions, is one of the dominant proteins found in Lewy Bodies, a pathological hallmark of Lewy body disorders, including Parkinson's disease (PD). More recently, α-Syn has been found in body fluids, including blood and cerebrospinal fluid, and is likely produced by both peripheral tissues and the central nervous system. Exchange of α-Syn between the brain and peripheral tissues could have important pathophysiologic and therapeutic implications. However, little is known about the ability of α-Syn to cross the blood–brain barrier (BBB). Here, we found that radioactively labeled α-Syn crossed the BBB in both the brain-to-blood and the blood-to-brain directions at rates consistent with saturable mechanisms. Low-density lipoprotein receptor-related protein-1 (LRP-1), but not p-glycoprotein, may be involved in α-Syn efflux and lipopolysaccharide (LPS)-induced inflammation could increase α-Syn uptake by the brain by disrupting the BBB.
ISSN:0196-9781
1873-5169
DOI:10.1016/j.peptides.2014.09.018