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Delivery-mediated exosomal therapeutics in ischemia-reperfusion injury: advances, mechanisms, and future directions.
Ding, Shengzhe; Kim, Yu-Jin; Huang, Kai-Yu; Um, Daniel; Jung, Youngmee; Kong, Hyunjoon.
Afiliação
  • Ding S; Chemical & Biomolecular Engineering, University of Illinois, Urbana, IL, 61801, USA.
  • Kim YJ; Center for Biomaterials, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.
  • Huang KY; Chemical & Biomolecular Engineering, University of Illinois, Urbana, IL, 61801, USA.
  • Um D; Bioengineering, University of Illinois, Urbana, IL, 61801, USA.
  • Jung Y; Center for Biomaterials, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.
  • Kong H; Department of Electrical and Electronic Engineering, YU-KIST Institute, Yonsei University, Seoul, 03722, Republic of Korea.
Nano Converg ; 11(1): 18, 2024 Apr 30.
Article em En | MEDLINE | ID: mdl-38689075
ABSTRACT
Ischemia-reperfusion injury (IRI) poses significant challenges across various organ systems, including the heart, brain, and kidneys. Exosomes have shown great potentials and applications in mitigating IRI-induced cell and tissue damage through modulating inflammatory responses, enhancing angiogenesis, and promoting tissue repair. Despite these advances, a more systematic understanding of exosomes from different sources and their biotransport is critical for optimizing therapeutic efficacy and accelerating the clinical adoption of exosomes for IRI therapies. Therefore, this review article overviews the administration routes of exosomes from different sources, such as mesenchymal stem cells and other somatic cells, in the context of IRI treatment. Furthermore, this article covers how the delivered exosomes modulate molecular pathways of recipient cells, aiding in the prevention of cell death and the promotions of regeneration in IRI models. In the end, this article discusses the ongoing research efforts and propose future research directions of exosome-based therapies.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nano Converg Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nano Converg Ano de publicação: 2024 Tipo de documento: Article