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| Auteurs principaux: | , |
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| Format: | Preprint |
| Publié: |
2024
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| Accès en ligne: | https://arxiv.org/abs/2404.10915 |
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| _version_ | 1866913902030225408 |
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| author | Amato, Sara Arnold, Andrea |
| author_facet | Amato, Sara Arnold, Andrea |
| contents | Neuroinflammation immediately follows the onset of ischemic stroke. During this process, microglial cells are activated in and recruited to the tissue surrounding the irreversibly injured infarct core, referred to as the penumbra. Microglial cells can be activated into two distinct phenotypes; however, the dynamics between the detrimental M1 phenotype and beneficial M2 phenotype are not fully understood. Using phenotype-specific cell count data obtained from experimental studies on middle cerebral artery occlusion-induced stroke in mice, we employ sparsity-promoting system identification techniques combined with Bayesian statistical methods for uncertainty quantification to generate continuous and discrete-time predictive models of the M1 and M2 microglial cell dynamics. The resulting data-driven models include constant and linear terms but do not include nonlinear interactions between the cells. Results emphasize an initial M2 dominance followed by a takeover of M1 cells, capture potential long-term dynamics of microglial cells, and suggest a persistent inflammatory response. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2404_10915 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Data-driven modeling and prediction of microglial cell dynamics in the ischemic penumbra Amato, Sara Arnold, Andrea Cell Behavior Quantitative Methods Applications Computation Neuroinflammation immediately follows the onset of ischemic stroke. During this process, microglial cells are activated in and recruited to the tissue surrounding the irreversibly injured infarct core, referred to as the penumbra. Microglial cells can be activated into two distinct phenotypes; however, the dynamics between the detrimental M1 phenotype and beneficial M2 phenotype are not fully understood. Using phenotype-specific cell count data obtained from experimental studies on middle cerebral artery occlusion-induced stroke in mice, we employ sparsity-promoting system identification techniques combined with Bayesian statistical methods for uncertainty quantification to generate continuous and discrete-time predictive models of the M1 and M2 microglial cell dynamics. The resulting data-driven models include constant and linear terms but do not include nonlinear interactions between the cells. Results emphasize an initial M2 dominance followed by a takeover of M1 cells, capture potential long-term dynamics of microglial cells, and suggest a persistent inflammatory response. |
| title | Data-driven modeling and prediction of microglial cell dynamics in the ischemic penumbra |
| topic | Cell Behavior Quantitative Methods Applications Computation |
| url | https://arxiv.org/abs/2404.10915 |