Novel SCRG1/BST1 axis regulates self-renewal, migration, and osteogenic differentiation potential in mesenchymal stem cells

被引:55
作者
Aomatsu, Emiko [1 ,2 ]
Takahashi, Noriko [1 ]
Sawada, Shunsuke [3 ,4 ]
Okubo, Naoto [1 ]
Hasegawa, Tomokazu [5 ]
Taira, Masayuki [6 ]
Miura, Hiroyuki [2 ]
Ishisaki, Akira [1 ]
Chosa, Naoyuki [1 ]
机构
[1] Iwate Med Univ, Dept Biochem, Div Cellular Biosignal Sci, Yahaba, Iwate 0283694, Japan
[2] Iwate Med Univ, Sch Dent, Dept Dev Oral Hlth Sci, Div Orthodont, Morioka, Iwate 0208505, Japan
[3] Iwate Med Univ, Sch Dent, Dept Conservat Dent, Div Periodontol, Morioka, Iwate 0208505, Japan
[4] Iwate Med Univ, Sch Dent, Clin Res Lab, Morioka, Iwate 0208505, Japan
[5] Tokushima Univ Hosp, Dept Pediat Dent, Tokushima 7708504, Japan
[6] Iwate Med Univ, Dept Biomed Engn, Yahaba, Iwate 0283694, Japan
关键词
HUMAN BONE-MARROW; FOCAL ADHESION KINASE; STROMAL CELLS; IN-VITRO; CD157; GENE; EXPRESSION; SCRAPIE; BST-1; REGENERATION;
D O I
10.1038/srep03652
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human mesenchymal stem cells (hMSCs) remodel or regenerate various tissues through several mechanisms. Here, we identified the hMSC-secreted protein SCRG1 and its receptor BST1 as a positive regulator of self-renewal, migration, and osteogenic differentiation. SCRG1 and BST1 gene expression decreased during osteogenic differentiation of hMSCs. Intriguingly, SCRG1 maintained stem cell marker expression (Oct-4 and CD271/LNGFR) and the potentials of self-renewal, migration, and osteogenic differentiation, even at high passage numbers. Thus, the novel SCRG1/BST1 axis determines the fate of hMSCs by regulating their kinetic and differentiation potentials. Our findings provide a new perspective on methods for ex vivo expansion of hMSCs that maintain native stem cell potentials for bone-forming cell therapy.
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页数:9
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