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COTiR:基于合成外泌体的组织再生的分子通信模型。

COTiR: Molecular Communication Model for Synthetic Exosome-Based Tissue Regeneration.

出版信息

IEEE Trans Nanobioscience. 2024 Jan;23(1):202-209. doi: 10.1109/TNB.2023.3302773. Epub 2024 Jan 3.

Abstract

Mesenchymal stem cell (MSC)-derived exosomes are recognized as an unparalleled therapy for tissue damage rendered by COVID-19 infection and subsequent hyper-inflammatory immune response. However, the natural targeting mechanism of exosomes is challenging to detect the damaged tissue over long diffusion distances efficiently. The coordinated movement of exosomes is desired for successful identification of target sites. In this work, we propose a molecular communication model, CoTiR, with a bio-inspired directional migration strategy (DMS) for guided propagation of exosomes to target the damaged tissues. The model includes directional propagation, reception, and regeneration of tissue. The proposed model has the potential to be used in designing efficient communication systems in the nanodomain. We compare the proposed model to the basic random propagation model and show the efficacy of our model regarding the detection of multiple targets and the detection time required. Simulation results indicate that the proposed model requires a shorter period of time for a similar number of exosomes to detect the targets compared to the basic random propagation model. Furthermore, the results reveal a 99.96% decrease in the collagen concentration in the absence of inflammatory cytokine molecules compared to the collagen concentration in the presence of inflammatory cytokine molecules.

摘要

间充质干细胞 (MSC) 衍生的外泌体被认为是治疗 COVID-19 感染和随后的过度炎症免疫反应导致的组织损伤的一种无与伦比的疗法。然而,外泌体的天然靶向机制很难有效地检测到远距离的受损组织。外泌体的协调运动对于成功识别靶标位点是必要的。在这项工作中,我们提出了一个分子通信模型 CoTiR,它具有生物启发的定向迁移策略 (DMS),用于引导外泌体传播以靶向受损组织。该模型包括组织的定向传播、接收和再生。该模型有可能用于设计纳米域中的高效通信系统。我们将所提出的模型与基本的随机传播模型进行了比较,并展示了我们的模型在检测多个目标和所需的检测时间方面的有效性。模拟结果表明,与基本的随机传播模型相比,我们的模型在检测目标时需要更短的时间来使用相同数量的外泌体。此外,结果显示与存在炎症细胞因子分子时的胶原蛋白浓度相比,在不存在炎症细胞因子分子时胶原蛋白浓度降低了 99.96%。

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