Regenerative Medicine Unit, Division of Applied Medicine, University of Aberdeen, Aberdeen, UK.
Eur Cell Mater. 2010 Sep 1;20:121-33. doi: 10.22203/ecm.v020a11.
Mesenchymal Stromal Progenitor/Stem Cells (MSCs) are a rare population of non-hematopoietic stromal cells, present in the bone marrow and most connective tissues of the body. They are capable of differentiation into mesenchymal tissues such as bone, cartilage, adipose tissue and muscle. In the absence of specific markers, MSCs have been defined following isolation and culture expansion, by their expression of various molecules including CD90, CD105 and CD73 and absence of markers like CD34, CD45, and CD14. MSCs have extensive proliferative ability in culture in an uncommitted state while retaining their multilineage differentiation potential, which make them attractive candidates for biological cell-based tissue repair approaches. However, their identity in their tissues of origin is not clear and the niches in which they reside are not defined. This review addresses the current state of MSC research including the differentiation potency of culture expanded MSCs, expression of chemokines and their receptors in MSCs--both relevant issues for the advocated use of MSCs for tissue repair and their systemic delivery to the affected tissues. It also reviews current knowledge of MSC niches in their native tissues, addressing the relationship with pericytes. Finally, it provides a scientific basis for the requirement of a thorough characterisation of the endogenous MSC niches within their native tissues in vivo. The knowledge of MSC niches will instruct development of innovative therapeutic measures such as producing pharmacological substances that target endogenous MSCs and their niches in order to activate and guide intrinsic repair and to improve disease outcomes.
间充质基质祖细胞/干细胞(MSCs)是一种罕见的非造血基质细胞群,存在于骨髓和身体的大多数结缔组织中。它们能够分化为间充质组织,如骨、软骨、脂肪组织和肌肉。在缺乏特定标记物的情况下,MSC 可以通过其表达各种分子(包括 CD90、CD105 和 CD73)和缺乏标记物(如 CD34、CD45 和 CD14)来定义,这些分子在分离和培养扩增后被定义。MSC 在未分化状态下具有广泛的增殖能力,同时保持其多谱系分化潜能,这使它们成为生物细胞基组织修复方法的有吸引力的候选者。然而,它们在其组织起源中的身份尚不清楚,其所在的生态位也未定义。本综述讨论了 MSC 研究的现状,包括培养扩增的 MSC 的分化潜能、MSC 中趋化因子及其受体的表达--这些都是提倡将 MSC 用于组织修复及其向受损组织的全身输送的相关问题。它还回顾了 MSC 固有组织中生态位的当前知识,涉及与周细胞的关系。最后,它为在体内对其固有组织中内源性 MSC 生态位进行彻底特征描述的要求提供了科学依据。了解 MSC 生态位将为开发创新的治疗措施提供指导,例如产生靶向内源性 MSC 及其生态位的药理学物质,以激活和指导内在修复,并改善疾病结局。