Extracellular Matrix Regulation of Stem Cell Fate

被引:7
作者
Smith Q. [1 ]
Gerecht S. [1 ,2 ]
机构
[1] Department of Chemical and Biomolecular Engineering, Physical Sciences-Oncology Center and the Institute for NanoBioTechnology, Johns Hopkins University, Baltimore, 21218, MD
[2] Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, 21218, MD
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Cell fate; Hydrogels; Material science; Mesenchymal stem cells; Stem cell differentiation; Tissue engineering;
D O I
10.1007/s40778-018-0111-2
中图分类号
学科分类号
摘要
Purpose of Review: The extracellular matrix (ECM) presents a complex myriad of biochemical and physical cues in the stem cell niche and is able to modulate stem cell fate and function. This review summarizes engineering approaches that have exploited natural and synthetic biomaterials to understand ECM regulation of stem cell fate. Specifically, we demonstrate how these studies have advanced our understanding of vascular maturation and mesenchymal lineage specification. Recent Findings: ECM mechanics have emerged as a critical cue in stem cell lineage specification. With the introduction of mechanically dynamic materials, which mirror the non-linear elastic behavior of natural matrices, our understanding of differentiation behavior has evolved. Summary: While studies using conventional culture employing rigid, two-dimensional surfaces have greatly advanced our understanding of stem cell differentiation, they overlook the complexity of ECM in the stem cell environment. Implementing defined analogs, through material science and tissue engineering approaches, will allow us to mirror the dynamic nature of ECM and fully elucidate how stem cells differentiate. © 2018, Springer International Publishing AG, part of Springer Nature.
引用
收藏
页码:13 / 21
页数:8
相关论文
共 61 条
  • [1] Ingber D., Extracellular matrix and cell shape: potential control points for inhibition of angiogenesis, J Cell Biochem, 47, 3, pp. 236-241, (1991)
  • [2] Raab M., Swift J., Dingal P.C.D., Shah P., Shin J.-W., Discher D.E., Crawling from soft to stiff matrix polarizes the cytoskeleton and phosphoregulates myosin-II heavy chain, J Cell Biol, 199, 4, pp. 669-683, (2012)
  • [3] Lo C.-M., Wang H.-B., Dembo M., Wang Y.-L., Cell movement is guided by the rigidity of the substrate, Biophys J, 79, 1, pp. 144-152, (2000)
  • [4] Wang N., Ingber D.E., Control of cytoskeletal mechanics by extracellular matrix, cell shape, and mechanical tension, Biophys J, 66, 6, pp. 2181-2189, (1994)
  • [5] Prasain N., Lee M.R., Vemula S., Meador J.L., Yoshimoto M., Ferkowicz M.J., Fett A., Gupta M., Rapp B.M., Saadatzadeh M.R., Ginsberg M., Elemento O., Lee Y., Voytik-Harbin S.L., Chung H.M., Hong K.S., Reid E., O'Neill C.L., Medina R.J., Stitt A.W., Murphy M.P., Rafii S., Broxmeyer H.E., Yoder M.C., Differentiation of human pluripotent stem cells to cells similar to cord-blood endothelial colony-forming cells, Nat Biotechnol, 32, 11, pp. 1151-1157, (2014)
  • [6] Dickinson L.E., Kusuma S., Gerecht S., Reconstructing the differentiation niche of embryonic stem cells using biomaterials, Macromol Biosci, 11, 1, pp. 36-49, (2011)
  • [7] Levental I., Georges P.C., Janmey P.A., Soft biological materials and their impact on cell function, Soft Matter, 3, 3, pp. 299-306, (2007)
  • [8] Wells R.G., The role of matrix stiffness in regulating cell behavior, Hepatology, 47, 4, pp. 1394-1400, (2008)
  • [9] Kim I.L., Mauck R.L., Burdick J.A., Hydrogel design for cartilage tissue engineering: a case study with hyaluronic acid, Biomaterials, 32, 34, pp. 8771-8782, (2011)
  • [10] Schaffler M.B., Burr D.B., Stiffness of compact bone: effects of porosity and density, J Biomech, 21, 1, pp. 13-16, (1988)