bioRxivPharmacology & ToxicologyPreprint
Biomaterial based implants caused remote liver fatty deposition through activated blood-derived Kupffer cells
Z. Peng, C. Xie, S. Jin, J. Hu, X. Yao, J. Ye, X. Zhang, J. X. Lim, B. Wu, H. Wu, R. Liang, Y. Wen, J. Huang, X. Zou, O. Hongwei
Abstract
Understanding the foreign-body response (FBR) of biomaterials is a prerequisite for the prediction of its clinical application, and the present assessments mainly rely on in vitro cell culture and in situ histopathology. However, remote organs responses after biomaterials implantation is unclear. Here, by leveraging body-wide-transcriptomics data, we performed in-depth systems analysis of biomaterials - remote organs crosstalk after abdominal implantation of polypropylene and silk fibroin using a rodent model, demonstrating local implantation caused remote organs responses dominated by acute-phase responses, immune system responses and lipid metabolism disorders. Of note, liver function was specially disturbed, defined as hepatic lipid deposition. Combining flow cytometry analyses and liver monocyte recruitment inhibition experiments, we proved that blood derived monocyte-derived Kupffer cells in the liver underlying the mechanism of abnormal lipid deposition induced by local biomaterials implantation. Moreover, from the perspective of temporality, the remote organs responses and liver lipid deposition of silk fibroin group faded away with biomaterial degradation and restored to normal at end, which highlighted its superiority of degradability. These findings were further indirectly evidenced by human blood biochemical examination from 141 clinical cases of hernia repair using silk fibroin mesh and polypropylene mesh. In conclusion, this study provided knowledge of biomaterials-body interactions. It is of great important for future development of biomaterial devices for clinical application. One Sentence SummaryAbdominal local biomaterials implantation induces remote organ fatty deposition through activated blood-derived Kupffer cells.
- organism: mouse
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- approach: statistical model
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Murine gut microbiota dysbiosis via enteric infection modulates the foreign body response to a distal biomaterial implant
Brenda Yang, Natalie Rutkowski, … Jennifer H. Elisseeff·Proceedings of the National Academy of SciencesPeer-reviewed·May 12, 2025
- FIBRIN POLYMER ON THE SURFACE OF BIOMATERIAL IMPLANTS DRIVES THE FOREIGN BODY REACTION
A. Balabiyev, N. P. Podolnikova, … T. P. Ugarova·bioRxiv·Feb 16, 2021
- Biomaterials direct functional B cell response in a material specific manner
E. Moore, D. R. Maestas, … J. H. Elisseeff·bioRxiv·Jan 12, 2021
- An extracellular matrix coating similar to articular cartilage inhibits the differentiation of myofibroblasts and limits the development of implant-induced fibrosis
Melis Ozkan, Michael J. V. White, … Jeffrey A. Hubbell·bioRxiv·Sep 10, 2025
- Live imaging the Foreign Body Response reveals how dampening inflammation reduces fibrosis
D. Gurevich, K. French, … P. Martin·bioRxiv·May 9, 2019
- Macrophage microRNA-146a is a central regulator of the foreign body response to biomaterial implants
M. Mahanty, B. Dutta, … S. O. Rahaman·bioRxiv·Apr 3, 2024