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

Author:

Gilbert P. M.1,Havenstrite K. L.12,Magnusson K. E. G.13,Sacco A.1,Leonardi N. A.14,Kraft P.1,Nguyen N. K.1,Thrun S.5,Lutolf M. P.4,Blau H. M.1

Affiliation:

1. Baxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.

3. School of Electrical Engineering, Signal Processing Lab, Royal Institute of Technology (KTH), SE-100 44 Stockholm, Sweden.

4. Institute of Bioengineering and Laboratory of Stem Cell Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.

5. Stanford Artificial Intelligence Lab, Department of Computer Science, Stanford, CA 94305, USA.

Abstract

Environment Matters Stem cells isolated from muscle can be used for muscle regeneration, but only if the stem cells are fresh. Under standard cell culture conditions in the laboratory, muscle stem cells fail to proliferate efficiently and lose their regenerative capacity. Gilbert et al. (p. 1078 , published online 15 July; see the Perspective by Bhatia ) built an in vitro–culture system that resembles the physical characteristics in which muscle stem cells normally reside: a squishy elastic bed (rather than the hard slab of a plastic culture flask). Laminin tethered to hydrogels was used to generate substrates of varying elasticity. When cultured on these substrates, muscle stem cells remained undifferentiated and were able to support muscle regeneration when transplanted back into mice.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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