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On human pluripotent stem cell control: The rise of 3D bioengineering and mechanobiology

期刊

BIOMATERIALS
卷 52, 期 -, 页码 26-43

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.01.078

关键词

Human pluripotent stem cells; Mechanobiology; Bioengineering; Regenerative medicine; Development; Human disease modeling

资金

  1. National Science Foundation [CMMI 1129611, CBET 1149401, ECCS 1231826, CBET 1263889]
  2. National Institutes of Health [R21 HL114011, R21 EB017078, R01 HL119542]
  3. American Heart Association [12SDG12180025]
  4. Department of Mechanical Engineering at the University of Michigan, Ann Arbor
  5. Directorate For Engineering [1149401] Funding Source: National Science Foundation
  6. Div Of Chem, Bioeng, Env, & Transp Sys [1149401] Funding Source: National Science Foundation

向作者/读者索取更多资源

Human pluripotent stem cells (hPSCs) provide promising resources for regenerating tissues and organs and modeling development and diseases in vitro. To fulfill their promise, the fate, function, and organization of hPSCs need to be precisely regulated in a three-dimensional (3D) environment to mimic cellular structures and functions of native tissues and organs. In the past decade, innovations in 3D culture systems with functional biomaterials have enabled efficient and versatile control of hPSC fate at the cellular level. However, we are just at the beginning of bringing hPSC-based regeneration and development and disease modeling to the tissue and organ levels. In this review, we summarize existing bioengineered culture platforms for controlling hPSC fate and function by regulating inductive mechanical and biochemical cues coexisting in the synthetic cell microenvironment. We highlight recent excitements in developing 3D hPSC-based in vitro tissue and organ models with in vivolike cellular structures, interactions, and functions. We further discuss an emerging multifaceted mechanotransductive signaling network with transcriptional coactivators YAP and TAZ at the center stage that regulate fates and behaviors of mammalian cells, including hPSCs. Future development of 3D biomaterial systems should incorporate dynamically modulated mechanical and chemical properties targeting specific intracellular signaling events leading to desirable hPSC fate patterning and functional tissue formation in 3D. (C) 2015 Elsevier Ltd. All rights reserved.

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