Concise Review: MicroRNA Function in Multipotent Mesenchymal Stromal Cells

被引:145
作者
Clark, Elizabeth A. [1 ]
Kalomoiris, Stefanos [1 ]
Nolta, Jan A. [1 ]
Fierro, Fernando A. [1 ]
机构
[1] Univ Calif Davis, Stem Cell Program, Davis, CA 95616 USA
关键词
microRNA; Marrow stromal stem cells; Mesenchymal stem cells; REGULATES OSTEOGENIC DIFFERENTIATION; STEM-CELLS; BONE-MARROW; OSTEOBLAST DIFFERENTIATION; ADIPOGENIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; ISCHEMIC ANGIOGENESIS; LINEAGE COMMITMENT; NEGATIVE REGULATOR; SIGNALING PATHWAY;
D O I
10.1002/stem.1623
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Multipotent mesenchymal stromal cells (MSCs) are ideal candidates for different cellular therapies due to their simple isolation, extensive expansion potential, and low immunogenicity. For various therapeutic approaches, such as bone and cartilage repair, MSCs are expected to contribute by direct differentiation to replace the damaged tissue, while many other applications rely on the secretion of paracrine factors which modulate the immune response and promote angiogenesis. MicroRNAs (miRNAs), which target messenger RNA for cleavage or translational repression, have recently been shown to play critical functions in MSC to regulate differentiation, paracrine activity, and other cellular properties such as proliferation, survival, and migration. The global miRNA expression profile of MSC varies according to the tissue of origin, species, and detection methodology, while also certain miRNAs are consistently found in all types of MSC. The function in MSC of more than 60 different miRNAs has been recently described, which is the subject of this review. A special emphasis is given to miRNAs that have demonstrated a function in MSC in vivo. We also present in detail miRNAs with overlapping effects (i.e., common target genes) and discuss future directions to deepen our understanding of miRNA biology in MSC. These recent discoveries have opened the possibility of modulating miRNAs in MSC, in order to enhance their proregenerative, therapeutic potential. Stem Cells 2014;32:1074-1082
引用
收藏
页码:1074 / 1082
页数:9
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