Isolation and Characterization of Milk Exosomes for Use in Advanced Therapies
Ana Medel-Martinez,
Ana Redrado-Osta,
Alejandra Crespo-Barreda,
Maria Sancho-Albero,
Lourdes Sánchez,
Víctor Sebastián,
María Pardo,
Antonio de la Vieja,
Pilar Martín-Duque
Affiliations
Ana Medel-Martinez
Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón), 50009 Zaragoza, Spain
Ana Redrado-Osta
Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón), 50009 Zaragoza, Spain
Alejandra Crespo-Barreda
Instituto Aragonés de Ciencias de la Salud (IACS), 50009 Zaragoza, Spain
Maria Sancho-Albero
Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón), 50009 Zaragoza, Spain
Lourdes Sánchez
Instituto Agroalimentario de Aragón, University of Zaragoza, 50018 Zaragoza, Spain
Víctor Sebastián
Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón), 50009 Zaragoza, Spain
María Pardo
Grupo Obesidómica, Área de Endocrinología, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), CIBEROBN (ISCIII), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), 15706 Santiago de Compostela, Spain
Antonio de la Vieja
Endocrine Tumors Unit, Chronic Disease Program (UFIEC), Instituto de Salud Carlos III, 28222 Majadahonda, Spain
Pilar Martín-Duque
Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón), 50009 Zaragoza, Spain
Exosomes are cell-derived extracellular vesicles (EVs) with diameters between 30 and 120 nm. In recent years, several studies have evaluated the therapeutic potential of exosomes derived from different fluids due to their low immunogenicity and high biocompatibility. However, producing exosomes on a large scale is still challenging. One of the fluids from which they could be isolated in large quantities is milk. Moreover, regeneration is a well-known property of milk. The present work seeks to optimize a method for isolating exosomes from bovine and human milk, comparing different storage conditions and different extraction protocols. We found differences in the yield extraction associated with pre-storage milk conditions and observed some differences according to the processing agent. When we removed milk fat globules and added rennet before freezing, we obtained a cleaner final fraction. In summary, we attempted to optimize a rennet-based new milk–exosome isolation method and concluded that pre-treatment, followed by freezing of samples, yielded the best exosome population.