Emerging Roles of Exosomes in Huntington's Disease

0542475 - ÚŽFG 2022 RIV CH eng J - Článek v odborném periodiku
Ananbeh, Hanadi - Vodička, Petr - Kupcová Skalníková, Helena
Emerging Roles of Exosomes in Huntington's Disease.
International Journal of Molecular Sciences. Roč. 22, č. 8 (2021), č. článku 4085. E-ISSN 1422-0067
Grant CEP: GA ČR(CZ) GA19-01747S; GA MŠMT(CZ) LTC18079
Institucionální podpora: RVO:67985904
Klíčová slova: extracellular vesicle * exosome * neurodegeneration * Huntington´s disease * huntingtin
Obor OECD: Biochemical research methods
Impakt faktor: 6.208, rok: 2021
Způsob publikování: Open access
https://www.mdpi.com/1422-0067/22/8/4085

Huntington's disease (HD) is a rare hereditary autosomal dominant neurodegenerative disorder, which is caused by expression of mutant huntingtin protein (mHTT) with an abnormal number of glutamine repeats in its N terminus, and characterized by intracellular mHTT aggregates (inclusions) in the brain. Exosomes are small extracellular vesicles that are secreted generally by all cell types and can be isolated from almost all body fluids such as blood, urine, saliva, and cerebrospinal fluid. Exosomes may participate in the spreading of toxic misfolded proteins across the central nervous system in neurodegenerative diseases. In HD, such propagation of mHTT was observed both in vitro and in vivo. On the other hand, exosomes might carry molecules with neuroprotective effects. In addition, due to their capability to cross blood-brain barrier, exosomes hold great potential as sources of biomarkers available from periphery or carriers of therapeutics into the central nervous system. In this review, we discuss the emerging roles of exosomes in HD pathogenesis, diagnosis, and therapy.
Trvalý link: http://hdl.handle.net/11104/0319879