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代谢性疾病中的器官间和跨细胞通讯:CMGH近期研究的见解

Interorgan and Transcellular Communication in Metabolic Disease: Insights From Recent CMGH Studies.

作者信息

Dong Tien S, Mayer Emeran

机构信息

Goodman-Luskin Microbiome Center, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California; Oppenheimer Center for Neurobiology of Stress and Reslience, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California; The Vatche and Tamar Manoukian Division of Digestive Diseases, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

Goodman-Luskin Microbiome Center, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California; Oppenheimer Center for Neurobiology of Stress and Reslience, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California; The Vatche and Tamar Manoukian Division of Digestive Diseases, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

出版信息

Cell Mol Gastroenterol Hepatol. 2025 May 8;19(8):101530. doi: 10.1016/j.jcmgh.2025.101530.

Abstract

The emergence of interorgan and transcellular signaling as a defining hallmark of metabolic disease has catalyzed a paradigm shift in gastroenterology and hepatology. Increasingly, the gut, liver, adipose tissue, immune system, and the nervous system are being understood as nodes in an integrated metabolic network rather than isolated organs. The gut microbiome and its metabolites, enteroendocrine signaling, bile acid regulation, and epithelial barrier functions now occupy center stage in dissecting the pathophysiology not only of gastroenterologic conditions, such as obesity, metabolic dysfunction-associated steatotic liver disease, and cirrhosis, but also of several disorders making up the chronic noncontagious disease epidemic. This paradigm shift is being driven by advances in molecular biology, systems biology, and computational modeling, which have enabled a holistic understanding of how communication between organs orchestrates metabolic homeostasis. Key to this understanding is the realization that local perturbations in 1 organ, such as gut microbial dysbiosis, can have systemic repercussions that affect distant organs, such as the liver or brain. This has redefined how researchers conceptualize disease progression and therapeutic interventions. Rather than focusing on a single tissue, there is increasing interest in identifying molecular messengers that mediate crosstalk between organ systems, such as microbial metabolites, enteroendocrine peptides, bile acids, and cytokines. In this review, we highlight 4 recent and impactful studies published in Cellular and Molecular Gastroenterology and Hepatology that exemplify these advances. Each study offers a unique window into the mechanisms by which gut-derived signals influence host metabolism and disease states. Together, they deepen the understanding of the complex dialogue between organs and open new avenues for therapeutic exploration. We conclude by discussing the implications of these findings and outlining emerging questions and future directions for the field.

摘要

器官间和跨细胞信号传导作为代谢性疾病的一个决定性标志的出现,催化了胃肠病学和肝病学领域的范式转变。越来越多的人认识到,肠道、肝脏、脂肪组织、免疫系统和神经系统是一个综合代谢网络中的节点,而不是孤立的器官。肠道微生物群及其代谢产物、肠内分泌信号传导、胆汁酸调节和上皮屏障功能,现在不仅在剖析肥胖、代谢功能障碍相关脂肪性肝病和肝硬化等胃肠疾病的病理生理学方面占据核心地位,而且在剖析构成慢性非传染性疾病流行的几种疾病方面也占据核心地位。这种范式转变是由分子生物学、系统生物学和计算建模的进展推动的,这些进展使人们能够全面理解器官之间的通信如何协调代谢稳态。理解这一点的关键在于认识到一个器官中的局部扰动,如肠道微生物群失调,可能会产生影响远处器官(如肝脏或大脑)的全身影响。这重新定义了研究人员对疾病进展和治疗干预的概念化方式。研究人员不再专注于单一组织,而是越来越关注识别介导器官系统之间串扰的分子信使,如微生物代谢产物、肠内分泌肽、胆汁酸和细胞因子。在这篇综述中,我们重点介绍了发表在《细胞与分子胃肠病学与肝病学》上的4项近期且有影响力的研究,这些研究例证了这些进展。每项研究都为肠道衍生信号影响宿主代谢和疾病状态的机制提供了一个独特的视角。它们共同加深了对器官之间复杂对话的理解,并为治疗探索开辟了新途径。我们通过讨论这些发现的意义并概述该领域新出现的问题和未来方向来结束本文。

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