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Exosome release and cargo in Down syndrome.
Hamlett, Eric D; LaRosa, Angela; Mufson, Elliott J; Fortea, Juan; Ledreux, Aurélie; Granholm, Ann-Charlotte.
Afiliación
  • Hamlett ED; Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
  • LaRosa A; Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
  • Mufson EJ; Department of Neurobiology and Neurology, Barrow Neurological Institute, Phoenix, Arizona.
  • Fortea J; Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, CIBERNED, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Ledreux A; Alzheimer's Disease and Other Cognitive Disorders Unit, Department of Neurology, Hospital Clínic, Institut d'Investigació Biomèdica August Pi i Sunyer, University of Barcelona, Barcelona, Spain.
  • Granholm AC; Department of Biological Sciences and the Knoebel Institute for Healthy Aging, University of Denver, Denver, Colorado.
Dev Neurobiol ; 79(7): 639-655, 2019 07.
Article en En | MEDLINE | ID: mdl-31347291
ABSTRACT
Down syndrome (DS) is a multisystem disorder affecting 1 in 800 births worldwide. Advancing technology, medical treatment, and social intervention have dramatically increased life expectancy, yet there are many etiologies of this disorder that are in need of further research. The advent of the ability to capture extracellular vesicles (EVs) in blood from specific cell types allows for the investigation of novel intracellular processes. Exosomes are one type of EVs that have demonstrated great potential in uncovering new biomarkers of neurodegeneration and disease, and also that appear to be intricately involved in the transsynaptic spread of pathogenic factors underlying Alzheimer's disease and other neurological diseases. Exosomes are nanosized vesicles, generated in endosomal multivesicular bodies (MVBs) and secreted by most cells in the body. Since exosomes are important mediators of intercellular communication and genetic exchange, they have emerged as a major research focus and have revealed novel biological sequelae involved in conditions afflicting the DS population. This review summarizes current knowledge on exosome biology in individuals with DS, both early in life and in aging individuals. Collectively these studies have demonstrated that complex multicellular processes underlying DS etiologies may include abnormal formation and secretion of extracellular vesicles such as exosomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Endocitosis / Exosomas / Vesículas Extracelulares Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Dev Neurobiol Asunto de la revista: BIOLOGIA / NEUROLOGIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Endocitosis / Exosomas / Vesículas Extracelulares Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Dev Neurobiol Asunto de la revista: BIOLOGIA / NEUROLOGIA Año: 2019 Tipo del documento: Article