3d cellular architecture affects microrna and protein cargo of extracellular vesicles. Rocha, S., Carvalho, J., Oliveira, P., Voglstaetter, M., Schvartz, D., Thomsen, A. R, Walter, N., Khanduri, R., Sanchez, J., Keller, A., Oliveira, C., & Nazarenko, I. Advanced Science, 6:1800948, February, 2019.
doi  abstract   bibtex   
The success of malignant tumors is conditioned by the intercellular communication between tumor cells and their microenvironment, with extracellular vesicles (EVs) acting as main mediators. While the value of 3D conditions to study tumor cells is well established, the impact of cellular architecture on EV content and function is not investigated yet. Here, a recently developed 3D cell culture microwell array is adapted for EV production and a comprehensive comparative analysis of biochemical features, RNA and proteomic profiles of EVs secreted by 2D vs 3D cultures of gastric cancer cells, is performed. 3D cultures are significantly more efficient in producing EVs than 2D cultures. Global upregulation of microRNAs and downregulation of proteins in 3D are observed, indicating their dynamic coregulation in response to cellular architecture, with the ADP-ribosylation factor 6 signaling pathway significantly downregulated in 3D EVs. The data strengthen the biological relevance of cellular architecture for production and cargo of EVs.
@Article{Rocha2019,
  author       = {Sara Rocha and Joana Carvalho and Patrícia Oliveira and Maren Voglstaetter and Domitille Schvartz and Andreas R Thomsen and Nadia Walter and Richa Khanduri and Jean-Charles Sanchez and Andreas Keller and Carla Oliveira and Irina Nazarenko},
  title        = {3d cellular architecture affects microrna and protein cargo of extracellular vesicles},
  journal      = {Advanced Science},
  year         = {2019},
  volume       = {6},
  issue        = {4},
  pages        = {1800948},
  issn         = {1800948},
  issn-linking = {1800948},
  month        = feb,
  abstract     = {The success of malignant tumors is conditioned by the intercellular communication between tumor cells and their microenvironment, with extracellular vesicles (EVs) acting as main mediators. While the value of 3D conditions to study tumor cells is well established, the impact of cellular architecture on EV content and function is not investigated yet. Here, a recently developed 3D cell culture microwell array is adapted for EV production and a comprehensive comparative analysis of biochemical features, RNA and proteomic profiles of EVs secreted by 2D vs 3D cultures of gastric cancer cells, is performed. 3D cultures are significantly more efficient in producing EVs than 2D cultures. Global upregulation of microRNAs and downregulation of proteins in 3D are observed, indicating their dynamic coregulation in response to cellular architecture, with the ADP-ribosylation factor 6 signaling pathway significantly downregulated in 3D EVs. The data strengthen the biological relevance of cellular architecture for production and cargo of EVs.},
  doi          = {10.1002/advs.201800948},
  pii          = {10.1002/advs.201800948},
}

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