Directional migration of mesenchymal stem cells under an SDF-1α gradient on a microfluidic device

被引:32
|
作者
Park, Siwan [1 ]
Jang, Hwanseok [1 ]
Kim, Byung Soo [2 ]
Hwang, Changmo [3 ]
Jeong, Gi Seok [3 ]
Park, Yongdoo [1 ]
机构
[1] Korea Univ, Coll Med, Biomed Sci Brain Korea 21, Dept Biomed Engn, Seoul, South Korea
[2] Korea Univ, Grad Sch Med, Dept Biomed Sci, Seoul, South Korea
[3] Asan Med Ctr, Asan Inst Life Sci, Biomed Engn Res Ctr, Seoul, South Korea
来源
PLOS ONE | 2017年 / 12卷 / 09期
基金
新加坡国家研究基金会;
关键词
CHEMOKINE RECEPTOR CXCR4; ENDOTHELIAL-CELLS; PROSTATE-CANCER; RHO-GTPASES; METASTASIS; INHIBITOR; MICE; CHEMOTAXIS; ACTIVATION; PLATFORM;
D O I
10.1371/journal.pone.0184595
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
Homing of peripheral stem cells is regulated by one of the most representative homing factors, stromal cell-derived factor 1 alpha (SDF-1 alpha), which specifically binds to the plasma membrane receptor CXCR4 of mesenchymal stem cells (MSCs) in order to initiate the signaling pathways that lead to directional migration and homing of stem cells. This complex homing process and directional migration of stem cells have been mimicked on a microfluidic device that is capable of generating a chemokine gradient within the collagen matrix and embedding endothelial cell (EC) monolayers to mimic blood vessels. On the microfluidic device, stem cells showed directional migration toward the higher concentration of SDF-1 alpha, whereas treatment with the CXCR4 antagonist AMD3100 caused loss of directionality of stem cells. Furthermore, inhibition of stem cell's main migratory signaling pathways, RhoROCK and Rac pathways, caused blockage of actomyosin and lamellipodia formation, decreasing the migration distance but maintaining directionality. Stem cell homing regulated by SDF-1 alpha caused directional migration of stem cells, while the migratory ability was affected by the activation of migration-related signaling pathways.
引用
收藏
页数:18
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