间充质干细胞在组织修复和医学治疗中的未来作用:现实和期望

K. Al-Anazi
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引用次数: 0

摘要

间充质干细胞;亚历山大·弗里登斯坦在20世纪60年代首次描述了这一现象;是异质的、非造血的、成体的多能基质祖细胞,能够自我更新并分化成各种细胞类型[1-8]。它们可以从多种来源分离,包括:骨髓(BM)(主要来源)、外周血、脐带血、羊水、胎盘、脂肪组织(AT)、牙髓、滑液、唾液腺、肝脏、肺、皮肤和骨骼肌[1-10]。MSCs具有以下显著特征:粘附在塑料容器上;分化成成骨细胞、脂肪细胞和软骨细胞的能力;流式细胞术检测CD105、CD73和CD90呈特征性阳性,CD45、CD34、CD11b、CD14、CD19、CD79a和人白细胞抗原(HLA)-DR呈特征性阴性[1,3,4,11-16]。然而,在某些情况下,从BM、AT和其他来源获得的MSCs可能表达CD34表面标记物[5-8,17]。此外,MSCs不表达显著的组织相容性复合物和免疫刺激分子。因此,它们逃避了免疫监视,在移植中的临床应用与移植物排斥反应无关[10]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Future Role of Mesenchymal Stem Cells in Tissue Repair and Medical Therapeutics: Realities and Expectations
Mesenchymal Stem Cells (MSCs); which were first described by Alexander Fridenstein in the 1960s; are heterogeneous, non-hematopoietic, adult multipotent stromal progenitor cells that are capable of self-renewal and differentiation into various cell types [1-8]. They can be isolated from various sources including: Bone Marrow (BM) which is the main source, peripheral blood, umbilical cord blood, amniotic fluid, placenta, Adipose Tissue (AT), dental pulp, synovial fluid, salivary glands, liver, lung, skin and skeletal muscles [1-10]. MSCs have the following distinguishing features: adherence to the plastic vessel; capacity to different into osteoblasts, adipocytes and chondrocytes; and being characteristically positive for CD105, CD73, and CD90 and characteristically negative for CD45, CD34, CD11b, CD14, CD19, CD79a, and human leukocyte antigen (HLA)-DR on flow cytometry [1,3,4,11-16]. However, under certain circumstances, MSCs obtained from BM, AT, and other sources may express CD34 surface markers [5-8,17]. Additionally, MSCs do not express significant histocompatibility complexes and immune stimulating molecules. Consequently, they escape immune surveillance and their clinical utilization in transplantation is not associated with graft rejection [10].
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