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用于成骨细胞谱系研究的视觉报告基因。

Visual reporters for study of the osteoblast lineage.

作者信息

Roeder Emilie, Matthews Brya G, Kalajzic Ivo

机构信息

Department of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT 06030, USA.

Department of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT 06030, USA; Department of Pathophysiology, University of Osijek, Osijek, Croatia.

出版信息

Bone. 2016 Nov;92:189-195. doi: 10.1016/j.bone.2016.09.004. Epub 2016 Sep 8.

Abstract

Advancing our understanding of osteoblast biology and differentiation is critical to elucidate the pathological mechanisms responsible for skeletal diseases such as osteoporosis. Histology and histomorphometry, the classical methods to study osteoblast biology, identify osteoblasts based on their location and morphology and ability to mineralize matrix, but do not clearly define their stage of differentiation. Introduction of visual transgenes into the cells of osteoblast lineage has revolutionized the field and resulted in a paradigm shift that allowed for specific identification and isolation of subpopulations within the osteoblast lineage. Knowledge acquired from the studies based on GFP transgenes has allowed for more precise interpretation of studies analyzing targeted overexpression or deletion of genes in the osteoblast lineage. Here, we provide a condensed overview of the currently available promoter-fluorescent reporter transgenic mice that have been generated and evaluated to varying extents. We cover different stages of the lineage as transgenes have been utilized to identify osteoprogenitors, pre-osteoblasts, osteoblasts, or osteocytes. We show that each of these promoters present with advantages and disadvantages. The studies based on the use of these reporter mice have improved our understanding of bone biology. They constitute attractive models to target osteoblasts and help to understand their cell biology.

摘要

深化我们对成骨细胞生物学和分化的理解对于阐明诸如骨质疏松症等骨骼疾病的病理机制至关重要。组织学和组织形态计量学作为研究成骨细胞生物学的经典方法,根据成骨细胞的位置、形态以及矿化基质的能力来识别它们,但并未明确界定其分化阶段。将可视化转基因导入成骨细胞谱系细胞中给该领域带来了变革,并导致了一种范式转变,使得能够特异性识别和分离成骨细胞谱系中的亚群。基于绿色荧光蛋白(GFP)转基因的研究获得的知识,使得对分析成骨细胞谱系中基因靶向过表达或缺失的研究有了更精确的解读。在此,我们简要概述了目前已生成并在不同程度上进行评估的启动子 - 荧光报告转基因小鼠。由于转基因已被用于识别骨祖细胞、前成骨细胞、成骨细胞或骨细胞,我们涵盖了该谱系的不同阶段。我们表明这些启动子各自都有优缺点。基于使用这些报告小鼠的研究增进了我们对骨生物学的理解。它们构成了靶向成骨细胞的有吸引力的模型,并有助于理解其细胞生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957b/5056847/c894297694b8/nihms816096f1.jpg

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