Substrate Elasticity Regulates Skeletal Muscle Stem Cell Self-Renewal in Culture

被引:1194
作者
Gilbert, P. M. [1 ]
Havenstrite, K. L. [1 ,2 ]
Magnusson, K. E. G. [1 ,3 ]
Sacco, A. [1 ]
Leonardi, N. A. [1 ,4 ,5 ]
Kraft, P. [1 ]
Nguyen, N. K. [1 ]
Thrun, S. [6 ]
Lutolf, M. P. [4 ,5 ]
Blau, H. M. [1 ]
机构
[1] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Sch Med, Baxter Lab Stem Cell Biol,Dept Microbiol & Immuno, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[3] Royal Inst Technol KTH, Signal Proc Lab, Sch Elect Engn, SE-10044 Stockholm, Sweden
[4] Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1015 Lausanne, Switzerland
[5] Ecole Polytech Fed Lausanne, Lab Stem Cell Bioengn, CH-1015 Lausanne, Switzerland
[6] Stanford Univ, Dept Comp Sci, Stanford Artificial Intelligence Lab, Stanford, CA 94305 USA
关键词
SATELLITE CELLS; REGENERATION; EXPANSION; FATES;
D O I
10.1126/science.1191035
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
Stem cells that naturally reside in adult tissues, such as muscle stem cells (MuSCs), exhibit robust regenerative capacity in vivo that is rapidly lost in culture. Using a bioengineered substrate to recapitulate key biophysical and biochemical niche features in conjunction with a highly automated single-cell tracking algorithm, we show that substrate elasticity is a potent regulator of MuSC fate in culture. Unlike MuSCs on rigid plastic dishes (similar to 10(6) kilopascals), MuSCs cultured on soft hydrogel substrates that mimic the elasticity of muscle (12 kilopascals) self-renew in vitro and contribute extensively to muscle regeneration when subsequently transplanted into mice and assayed histologically and quantitatively by noninvasive bioluminescence imaging. Our studies provide novel evidence that by recapitulating physiological tissue rigidity, propagation of adult muscle stem cells is possible, enabling future cell-based therapies for muscle-wasting diseases.
引用
收藏
页码:1078 / 1081
页数:4
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