| Literature DB >> 30797770 |
Bo-Yie Chen1, Cheyenne Wei-Hsuan Sung2, Chihchen Chen3, Chao-Min Cheng4, David Pei-Cheng Lin5, Chin-Te Huang6, Min-Yen Hsu7.
Abstract
Exosomes, also called extracellular vesicles (EVs), are membranous structures measuring between 40 and 100 nm. Exosomes, secreted by various cells of the human body into body fluids, contain protein, mRNA, miRNA, and signaling molecules. Physiologically, exosomes assist in the intercellular transport of protein and RNA. Immunologically, exosomes exhibit antigen-presenting capability. In recent studies, exosomes were found to be associated with the pathophysiology of cardiovascular, renal, neurological, and ocular diseases. In addition, exosomes may play a major role in cancer metastasis. Due to the extremely small size and scarcity of exosomes in living samples, many early studies utilized sucrose density gradient ultracentrifugation for exosome collection. However, sucrose density gradient ultracentrifugation is rather time consuming and requires large biological sample quantities. Newer exosome studies combined immunoaffinity and microfluidic system approaches for more efficient exosome collection. Our review summarizes existing methods for EV isolation and notes their advantages and disadvantages. These promising approaches are all characterized by isolation efficiency, and savings in cost, labor, and time. Optimization of current methods is a necessary step toward clinically-relevant diagnostic product production, but the fact that EVs are already widely used in disease diagnosis and treatment encourages continued efforts.Entities:
Mesh:
Year: 2019 PMID: 30797770 DOI: 10.1016/j.cca.2019.02.021
Source DB: PubMed Journal: Clin Chim Acta ISSN: 0009-8981 Impact factor: 3.786