Extracellular vesicles have been identified as pivotal mediators of intercellular communication with critical roles in physiological and pathological conditions. Via this route, several molecules (e.g., nucleic acids, proteins, metabolites) can be transferred to proximal and distant targets to convey specific information. Extracellular vesicle-associated cargo molecules have been proposed as markers of several disease conditions for their potential of tracking down the generating cell. Indeed, circulating extracellular vesicles may represent biomarkers of dysfunctional cellular quality control systems especially in conditions characterized by the accrual of intracellular misfolded proteins. Furthermore, the identification of extracellular vesicles as tools for the delivery of nucleic acids or other cargo molecules to diseased tissues makes these circulating shuttles possible targets for therapeutic development. The increasing interest in the study of extracellular vesicles as biomarkers resides mainly in the fact that the identification of peripheral levels of extracellular vesicle-associated proteins might reflect molecular events occurring in hardly accessible tissues, such as the brain, thereby serving as a "brain liquid biopsy". The exploitation of extracellular vesicles for diagnostic and therapeutic purposed might offer unprecedented opportunities to develop personalized approaches. Here, we discuss the bright and dark sides of extracellular vesicles in the setting of two main neurodegenerative diseases (i.e., Parkinson's and Alzheimer's diseases). A special focus will be placed on the possibility of using extracellular vesicles as biomarkers for the two conditions to enable disease tracking and treatment monitoring.
机构:
Univ Minnesota, Sch Nursing, 5-140 Weaver Densford Hall,308 Harvard St SE, Minneapolis, MN 55455 USA
Univ Minnesota, Med Ctr, 5-140 Weaver Densford Hall,308 Harvard St SE, Minneapolis, MN 55455 USAUniv Minnesota, Sch Nursing, 5-140 Weaver Densford Hall,308 Harvard St SE, Minneapolis, MN 55455 USA
机构:
Harvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USAHarvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USA
Shah, Ravi
Patel, Tushar
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Mayo Clin, Dept Transplantat, Jacksonville, FL 32224 USAHarvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USA
Patel, Tushar
Freedman, Jane E.
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Univ Massachusetts, Sch Med, Worcester, MA USAHarvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USA
Freedman, Jane E.
NEW ENGLAND JOURNAL OF MEDICINE,
2018,
379
(10):
: 958
-
966
机构:
Iuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, RomaniaIuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, Romania
Jurj, Ancuta
Ionescu, Calin
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Iuliu Hatieganu Univ Med & Pharm, Surg Dept 7, 8 Victor Babes St, Cluj Napoca 400012, Romania
Municipal Hosp, Surg Dept, Cluj Napoca 400139, RomaniaIuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, Romania
Ionescu, Calin
Berindan-Neagoe, Ioana
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机构:
Iuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, RomaniaIuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, Romania
Berindan-Neagoe, Ioana
Braicu, Cornelia
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机构:
Iuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, Romania
George Emil Palade Univ Med, Res Ctr Oncopathol & Translat Med CCOMT, Targu Mures 540139, RomaniaIuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca 400337, Romania