骨髓基质细胞/骨骼干细胞异质性生物学基础的最新进展。

Biomaterials Translational Pub Date : 2022-03-28 eCollection Date: 2022-01-01 DOI:10.12336/biomatertransl.2022.01.002
Deepika Arora, Pamela Gehron Robey
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引用次数: 0

摘要

根据过去几十年的研究,源自骨髓基质的自我更新骨骼系是骨骼组织工程的理想来源。然而,成骨前体(即骨髓来源的骨骼干细胞(SSCs))与骨髓基质的其他细胞(骨髓基质细胞,BMSCs)的标记及其在体内和体外的异质性仍有待澄清。本综述旨在强调:i) 将骨髓间充质干细胞/间充质干细胞与其他 "间充质干细胞/基质细胞 "区分开来的重要性;ii) 造成其异质性的因素,以及这些因素如何影响间充质干细胞向骨骼分化的潜力。还探讨了间充质干细胞富集、扩增及其对间充质干细胞表型的影响。此外,还重点介绍了新兴的单细胞 RNA 测序方法,以仔细研究 BMSC 群体中独特的 SSCs 群体及其固定的后代。了解异质性的相关因素,有助于研究人员改进策略,分离、鉴定和采用最佳培养方法和来源鉴定,以制定标准操作规程,开发可重复的干细胞移植物。然而,需要对异质性的分子基础有更科学的了解,这可从单细胞或克隆群体的高通量功能转录组学中获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Recent updates on the biological basis of heterogeneity in bone marrow stromal cells/skeletal stem cells.

Based on studies over the last several decades, the self-renewing skeletal lineages derived from bone marrow stroma could be an ideal source for skeletal tissue engineering. However, the markers for osteogenic precursors; i.e., bone marrowderived skeletal stem cells (SSCs), in association with other cells of the marrow stroma (bone marrow stromal cells, BMSCs) and their heterogeneous nature both in vivo and in vitro remain to be clarified. This review aims to highlight: i) the importance of distinguishing BMSCs/SSCs from other "mesenchymal stem/stromal cells", and ii) factors that are responsible for their heterogeneity, and how these factors impact on the differentiation potential of SSCs towards bone. The prospective role of SSC enrichment, their expansion and its impact on SSC phenotype is explored. Emphasis has also been given to emerging single cell RNA sequencing approaches in scrutinizing the unique population of SSCs within the BMSC population, along with their committed progeny. Understanding the factors involved in heterogeneity may help researchers to improvise their strategies to isolate, characterize and adopt best culture practices and source identification to develop standard operating protocols for developing reproducible stem cells grafts. However, more scientific understanding of the molecular basis of heterogeneity is warranted that may be obtained from the robust high-throughput functional transcriptomics of single cells or clonal populations.

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