Affiliations 

  • 1 School of Biosciences, Faculty of Health & Medical Sciences, Taylor's University, No. 1, Jalan Taylor's, 47500, Subang Jaya, Malaysia
  • 2 Ming Medical Services Sdn Bhd, D3-7 (1st Floor), Block D3, Dana 1 Commercial Centre, Jalan PJU 1A/46, 47301, Petaling Jaya, Selangor, Malaysia
  • 3 School of Pharmacy, Monash University Malaysia, 47500, Bandar Sunway, Selangor, Malaysia
  • 4 Department of Chemical and Environmental Engineering, Faculty of Engineering, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor Darul Ehsan, Malaysia
  • 5 Ming Medical Services Sdn Bhd, D3-7 (1st Floor), Block D3, Dana 1 Commercial Centre, Jalan PJU 1A/46, 47301, Petaling Jaya, Selangor, Malaysia. [email protected]
  • 6 School of Pharmacy, Faculty of Health & Medical Sciences, Taylor's University, No. 1, Jalan Taylor's, 47500, Subang Jaya, Malaysia. [email protected]
Mol Biotechnol, 2021 Sep;63(9):780-791.
PMID: 34061307 DOI: 10.1007/s12033-021-00339-2

Abstract

The objective of this study is to develop a simple protocol to isolate and characterise small extracellular vesicles (sEVs) from human umbilical cord-derived MSCs (hUC-MSCs). hUC-MSCs were characterised through analysis of morphology, immunophenotyping and multidifferentiation ability. SEVs were successfully isolated by ultrafiltration from the conditioned medium of hUC-MSCs. The sEVs' size distribution, intensity within a specific surface marker population were measured with zetasizer or nanoparticle tracking analysis. The expression of surface and internal markers of sEVs was also assessed by western blotting. Morphology of hUC-MSCs displayed as spindle-shaped, fibroblast-like adherent cells. Phenotypic analysis by flow cytometry revealed that hUC-MSCs expressed MSC surface marker, including CD90, CD73, CD105, CD44 and exhibited the capacity for osteogenic, adipogenic and chondrogenic differentiation. Populations of sEVs with CD9, CD63 and CD81 positive were detected with size distribution in the diameter of 63.2 to 162.5 nm. Typical sEVs biomarkers such as CD9, CD63, CD81, HSP70 and TSG101 were also detected with western blotting. Our study showed that sEVs from hUC-MSCs conditioned medium were successfully isolated and characterised. Downstream application of hUC-MSCs-sEVs will be further explored.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.