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骨免疫学的最新进展:骨骼与免疫系统相互作用的新动态

Updates on Osteoimmunology: What's New on the Cross-Talk Between Bone and Immune System.

作者信息

Ponzetti Marco, Rucci Nadia

机构信息

Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

出版信息

Front Endocrinol (Lausanne). 2019 Apr 18;10:236. doi: 10.3389/fendo.2019.00236. eCollection 2019.

Abstract

The term osteoimmunology was coined many years ago to describe the research field that deals with the cross-regulation between bone cells and the immune system. As a matter of fact, many factors that are classically considered immune-related, such as InterLeukins (i.e., IL-6, -11, -17, and -23), Tumor Necrosis Factor (TNF)-α, Receptor-Activator of Nuclear factor Kappa B (RANK), and its Ligand (RANKL), Nuclear Factor of Activated T-cell, cytoplasmatic-1 (NFATc1), and others have all been found to be crucial in osteoclast and osteoblast biology. Conversely, bone cells, which we used to think would only regulate each other and take care of remodeling bone, actually regulate immune cells, by creating the so-called "endosteal niche." Both osteoblasts and osteoclasts participate to this niche, either by favoring engraftment, or mobilization of Hematopoietic Stem Cells (HSCs). In this review, we will describe the main milestones at the base of the osteoimmunology and present the key cellular players of the bone-immune system cross-talk, including HSCs, osteoblasts, osteoclasts, bone marrow macrophages, osteomacs, T- and B-lymphocytes, dendritic cells, and neutrophils. We will also briefly describe some pathological conditions in which the bone-immune system cross-talk plays a crucial role, with the final aim to portray the state of the art in the mechanisms regulating the bone-immune system interplay, and some of the latest molecular players in the field. This is important to encourage investigation in this field, to identify new targets in the treatment of bone and immune diseases.

摘要

“骨免疫学”这一术语是多年前创造的,用于描述研究骨细胞与免疫系统之间相互调节的研究领域。事实上,许多传统上被认为与免疫相关的因子,如白细胞介素(即IL-6、-11、-17和-23)、肿瘤坏死因子(TNF)-α、核因子κB受体激活剂(RANK)及其配体(RANKL)、活化T细胞核因子细胞质1(NFATc1)等,都已被发现对破骨细胞和成骨细胞生物学至关重要。相反,我们过去认为只会相互调节并负责骨重塑的骨细胞,实际上通过创造所谓的“骨内膜微环境”来调节免疫细胞。成骨细胞和破骨细胞都参与了这个微环境,要么通过促进造血干细胞(HSC)的植入,要么通过促进其动员。在这篇综述中,我们将描述骨免疫学基础的主要里程碑,并介绍骨-免疫系统相互作用的关键细胞参与者,包括造血干细胞、成骨细胞、破骨细胞、骨髓巨噬细胞、骨巨噬细胞、T和B淋巴细胞、树突状细胞和中性粒细胞。我们还将简要描述一些骨-免疫系统相互作用起关键作用的病理状况,最终目的是描绘调节骨-免疫系统相互作用机制的现状以及该领域一些最新的分子参与者。这对于鼓励该领域的研究、确定治疗骨和免疫疾病的新靶点很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/e3829e91a41c/fendo-10-00236-g0001.jpg

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