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用于研究微生物群-肠-脑轴的体外和小型化体外研究。

Ex vivo and miniaturized in vitro to study microbiota-gut-brain axis.

作者信息

Yata Vinod Kumar

机构信息

Department of Molecular Biology, Central University of Andhrapradesh, Ananthapuramu - 515701, Andhrapradesh, India.

出版信息

3 Biotech. 2024 Nov;14(11):280. doi: 10.1007/s13205-024-04126-z. Epub 2024 Oct 24.

Abstract

The microbiota-gut-brain axis involves complex bidirectional communication through neural, immune, and endocrine pathways. Microbial metabolites, such as short-chain fatty acids, influence gut motility and brain function by interacting with gut receptors and modulating hormone release. Additionally, microbial components such as lipopolysaccharides and cytokines can cross the gut epithelium and the blood-brain barrier, impacting immune responses and cognitive function. Ex vivo models, which preserve gut tissue and neural segments, offer insight into localized gut-brain communication by allowing for detailed study of nerve excitability in response to microbial signals, but they are limited in systemic complexity. Miniaturized in vitro models, including organ-on-chip platforms, enable precise control of the cellular environment and simulate complex microbiota-host interactions. These systems allow for the study of microbial metabolites, immune responses, and neuronal activity, providing valuable insights into gut-brain communication. Despite challenges such as replicating long-term biological processes and integrating immune and hormonal systems, advancements in bioengineered platforms are enhancing the physiological relevance of these models, offering new opportunities for understanding the mechanisms of the microbiota-gut-brain axis. This review aims to describe the ex vivo and miniaturized in vitro models which are used to mimic the in vivo conditions and facilitate more precise studies of gut brain communication.

摘要

微生物群-肠-脑轴涉及通过神经、免疫和内分泌途径进行的复杂双向通信。微生物代谢产物,如短链脂肪酸,通过与肠道受体相互作用并调节激素释放来影响肠道蠕动和脑功能。此外,诸如脂多糖和细胞因子等微生物成分可穿过肠上皮和血脑屏障,影响免疫反应和认知功能。保留肠道组织和神经节段的离体模型,通过允许详细研究对微生物信号的神经兴奋性,为局部肠-脑通信提供了见解,但它们在系统复杂性方面存在局限性。小型化体外模型,包括芯片器官平台,能够精确控制细胞环境并模拟复杂的微生物群-宿主相互作用。这些系统允许研究微生物代谢产物、免疫反应和神经元活动,为肠-脑通信提供有价值的见解。尽管存在复制长期生物过程以及整合免疫和激素系统等挑战,但生物工程平台的进展正在提高这些模型的生理相关性,为理解微生物群-肠-脑轴的机制提供了新机会。本综述旨在描述用于模拟体内条件并促进对肠脑通信进行更精确研究的离体和小型化体外模型。

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