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来源于特定物种的哺乳动物 MSC:特征和应用。

Mammalian MSC from selected species: Features and applications.

机构信息

Department of Visceral, Transplantation, Thoracic and Vascular Surgery, Applied Molecular Hepatology Laboratory, University Hospital of Leipzig, Liebigstraße 21, Leipzig D-04103, Germany.

出版信息

Cytometry A. 2018 Jan;93(1):32-49. doi: 10.1002/cyto.a.23239. Epub 2017 Sep 14.

Abstract

Mesenchymal stromal/stem cells (MSC) are promising candidates for cellular therapy of different diseases in humans and in animals. Following the guidelines of the International Society for Cell Therapy, human MSC may be identified by expression of a specific panel of cell surface markers (CD105+, CD73+, CD90+, CD34-, CD14-, or CD11b-, CD79- or CD19-, HLA-DR-). In addition, multiple differentiation potential into at least the osteogenic, adipogenic, and chondrogenic lineage is a main criterion for MSC definition. Human MSC and MSC of a variety of mammals isolated from different tissues meet these criteria. In addition to the abovementioned, they express many more cell surface markers. Yet, these are not uniquely expressed by MSC. The gross phenotypic appearance like marker expression and differentiation potential is similar albeit not identical for MSC from different tissues and species. Similarly, MSC may feature different biological characteristics depending on the tissue source and the isolation and culture procedures. Their versatile biological qualities comprising immunomodulatory, anti-inflammatory, and proregenerative capacities rely largely on the migratory and secretory capabilities of MSC. They are attracted to sites of tissue lesion and secrete factors to promote self-repair of the injured tissue. This is a big perspective for clinical MSC applications in both veterinary and human medicine. Phase I/II clinical trials have been initiated to assess safety and feasibility of MSC therapies in acute and chronic disease settings. Yet, since the mode of MSC action in a specific disease environment is still unknown at large, it is mandatory to unravel the response of MSC from a given source onto a specific disease environment in suitable animal models prior to clinical applications. © 2017 International Society for Advancement of Cytometry.

摘要

间充质基质/干细胞(MSC)是人类和动物多种疾病细胞治疗的有前途的候选物。根据国际细胞治疗学会的指导原则,人 MSC 可以通过表达特定的细胞表面标志物(CD105+、CD73+、CD90+、CD34-、CD14-或 CD11b-、CD79-或 CD19-、HLA-DR-)来鉴定。此外,向至少成骨、成脂和成软骨谱系的多向分化潜能是 MSC 定义的主要标准。从不同组织中分离的人类 MSC 和各种哺乳动物的 MSC 都符合这些标准。除了上述标准外,它们还表达了更多的细胞表面标志物。然而,这些标志物并非 MSC 所特有。尽管来自不同组织和物种的 MSC 的大体表型外观(如标志物表达和分化潜能)相似,但并不完全相同。同样,MSC 可能因其组织来源以及分离和培养程序而具有不同的生物学特性。它们多功能的生物学特性,包括免疫调节、抗炎和促再生能力,在很大程度上依赖于 MSC 的迁移和分泌能力。它们被吸引到组织损伤部位,并分泌因子促进受损组织的自我修复。这是兽医和人类医学中临床 MSC 应用的一个重要前景。已经启动了 I/II 期临床试验,以评估急性和慢性疾病环境中 MSC 治疗的安全性和可行性。然而,由于 MSC 在特定疾病环境中的作用模式仍知之甚少,因此在临床应用之前,必须在合适的动物模型中阐明来自特定来源的 MSC 对特定疾病环境的反应。 © 2017 国际细胞推进协会。

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