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MicroRNAs Regulation Modulated Self-Renewal and Lineage Differentiation of Stem Cells

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Author(s): Liu, SP (Liu, Shih-Ping); Fu, RH (Fu, Ru-Huei); Yu, HH (Yu, Hsiu-Hui); Li, KW (Li, Kuo-Wei); Tsai, CH (Tsai, Chang-Hai); Shyu, WC (Shyu, Woei-Cherng); Lin, SZ (Lin, Shinn- Zong)

Title: MicroRNAs Regulation Modulated Self-Renewal and Lineage Differentiation of Stem Cells

Source: CELL TRANSPLANTATION, 18 (9): 1039-1045 2009 Language: English

Document Type: Proceedings Paper

Author Keywords: Posttranscriptional regulation; MicroRNAs; Stem cells

KeyWords Plus: MESENCHYMAL STROMAL CELLS; CENTRAL-NERVOUS-SYSTEM;

MURINE MODELS; ADULT-MOUSE; EXPRESSION; CANCER; STROKE; PCR;

QUANTIFICATION; IMPLANTATION

Abstract: Stem cells are unique cells in the ability that can self-renew and differentiate into a wide variety of cell types, suggesting that a specific molecular control network underlies these features. To date, stem cells have been applied to many clinical therapeutic approaches. For example, hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs) are the cells responding to ischemia or injury and engage in effective revascularization to repair within impairment regions. Transplantation of MSCs after stroke and hindlimb ischemia results in remarkable recovery through enhancing angiogenesis. MicroRNAs are a novel class of endogenous, small, noncoding RNAs that work via translational inhibition or degradation of their target mRNAs to downregulate gene expression. MicroRNAs have been strongly linked to stem cells, which have a remarkable role in development. In this study, we focused on the microRNA regulation in multiple stem cells. For example, miR-520h was upregulated and miR- 129 was downregulated in HSC. MiR-103, 107, 140, 143, 638, and 663 were associated with MSCs while miR-302s and miR-136 were associated with ESCs. In NSCs, miR-92b, let-7, and miR-125 were the critical regulators. This overview of the recent advances in the aspects of molecular control of stem cell biology reveals the importance of microRNAs, which may be helpful for future work.

Addresses: [Liu, Shih-Ping; Fu, Ru-Huei; Yu, Hsiu-Hui; Li, Kuo-Wei; Shyu, Woei-Cherng; Lin, Shinn-Zong] China Med Univ & Hosp, Ctr Neuropsychiat, Taichung, Taiwan; [Liu, Shih-Ping]

China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan; [Fu, Ru-Huei; Shyu, Woei- Cherng; Lin, Shinn-Zong] China Med Univ, Dept Immunol, Taichung, Taiwan; [Tsai, Chang- Hai] China Med Univ Hosp, Dept Pediat, Taichung, Taiwan; [Tsai, Chang-Hai] Asia Univ, Dept Healthcare Adm, Taichung, Taiwan; [Lin, Shinn-Zong] China Med Univ, Beigang Hosp, Yunlin, Taiwan

Reprint Address: Lin, SZ, China Med Univ & Hosp, Ctr Neuropsychiat, Taichung, Taiwan.

E-mail Address: [email protected]; [email protected]

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Cited Reference Count: 56 Times Cited: 2

Publisher: COGNIZANT COMMUNICATION CORP

Publisher Address: 3 HARTSDALE ROAD, ELMSFORD, NY 10523-3701 USA ISSN: 0963-6897

DOI: 10.3727/096368909X471224

29-char Source Abbrev.: CELL TRANSPLANT ISO Source Abbrev.: Cell Transplant.

Source Item Page Count: 7

Subject Category: Medicine, Research & Experimental; Transplantation ISI Document Delivery No.: 544ZA

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