Human adipose tissue-derived mesenchymal stem cells secrete functional neprilysin-bound exosomes

• Published in: Scientific reports Vol. 3; no. 1; p. 1197
• Main Authors: Katsuda, Takeshi, Tsuchiya, Reiko, Kosaka, Nobuyoshi, Yoshioka, Yusuke, Takagaki, Kentaro, Oki, Katsuyuki, Takeshita, Fumitaka, Sakai, Yasuyuki, Kuroda, Masahiko, Ochiya, Takahiro
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.02.2013; Nature Publishing Group
• Subjects: 631/378/340; 631/45/607/468; 631/532/2074; 631/61/2297; Adipose tissue; Adipose Tissue - cytology; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's disease; Amyloid beta-Peptides - metabolism; Bone marrow; Cells, Cultured; Exosomes; Exosomes - metabolism; Fluorescent Dyes - chemistry; Gene transfer; Humanities and Social Sciences; Humans; Mesenchymal stem cells; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - metabolism; Mesenchymal Stromal Cells - secretion; Mesenchyme; multidisciplinary; Nep gene; Neprilysin; Neprilysin - genetics; Neprilysin - metabolism; Neprilysin - secretion; Neurodegenerative diseases; Peptide Fragments - metabolism; Recombinant Proteins - biosynthesis; Recombinant Proteins - genetics; Science; Skin & tissue grafts; Stem cells; β-Amyloid
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep01197

Alzheimer's disease (AD) is characterized by the accumulation of β-amyloid peptide (Aβ) in the brain because of an imbalance between Aβ production and clearance. Neprilysin (NEP) is the most important Aβ-degrading enzyme in the brain. Thus, researchers have explored virus-mediated NEP gene delivery. However, such strategies may entail unexpected risks and thus exploration of a new possibility for NEP delivery is also required. Here, we show that human adipose tissue-derived mesenchymal stem cells (ADSCs) secrete exosomes carrying enzymatically active NEP. The NEP-specific activity level of 1 μg protein from ADSC-derived exosomes was equivalent to that of ~ 0.3 ng of recombinant human NEP. Of note, ADSC-derived exosomes were transferred into N2a cells and were suggested to decrease both secreted and intracellular Aβ levels in the N2a cells. Importantly, these characteristics were more pronounced in ADSCs than bone marrow-derived mesenchymal stem cells, suggesting the therapeutic relevance of ADSC-derived exosomes for AD.