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In vivo identification of apoptotic and extracellular vesicle-bound live cells using image-based deep learning.
Kranich, Jan; Chlis, Nikolaos-Kosmas; Rausch, Lisa; Latha, Ashretha; Schifferer, Martina; Kurz, Tilman; Foltyn-Arfa Kia, Agnieszka; Simons, Mikael; Theis, Fabian J; Brocker, Thomas.
Afiliação
  • Kranich J; Faculty of Medicine, Institute for Immunology, Munich, Germany.
  • Chlis NK; Institute of Computational Biology, Neuherberg, Germany.
  • Rausch L; Roche Pharma Research and Early Development, Large Molecule Research, Roche Innovation Center Munich, Penzberg, Germany.
  • Latha A; Faculty of Medicine, Institute for Immunology, Munich, Germany.
  • Schifferer M; Faculty of Medicine, Institute for Immunology, Munich, Germany.
  • Kurz T; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
  • Foltyn-Arfa Kia A; Munich Cluster of Systems Neurology (Synergy), Munich, Germany.
  • Simons M; Faculty of Medicine, Institute for Immunology, Munich, Germany.
  • Theis FJ; Faculty of Medicine, Institute for Immunology, Munich, Germany.
  • Brocker T; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
J Extracell Vesicles ; 9(1): 1792683, 2020 Jul 16.
Article em En | MEDLINE | ID: mdl-32944180
The in vivo detection of dead cells remains a major challenge due to technical hurdles. Here, we present a novel method, where injection of fluorescent milk fat globule-EGF factor 8 protein (MFG-E8) in vivo combined with imaging flow cytometry and deep learning allows the identification of dead cells based on their surface exposure of phosphatidylserine (PS) and other image parameters. A convolutional autoencoder (CAE) was trained on defined pictures and successfully used to identify apoptotic cells in vivo. However, unexpectedly, these analyses also revealed that the great majority of PS+ cells were not apoptotic, but rather live cells associated with PS+ extracellular vesicles (EVs). During acute viral infection apoptotic cells increased slightly, while up to 30% of lymphocytes were decorated with PS+ EVs of antigen-presenting cell (APC) exosomal origin. The combination of recombinant fluorescent MFG-E8 and the CAE-method will greatly facilitate analyses of cell death and EVs in vivo.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article