4.8 Article

Microdevice arrays with strain sensors for 3D mechanical stimulation and monitoring of engineered tissues

期刊

BIOMATERIALS
卷 172, 期 -, 页码 30-40

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.04.041

关键词

Microdevice; Mechanical stimulation; On-chip strain sensing; Tissue stiffness monitoring; Hydrogel; Mesenchymal stromal cell

资金

  1. Canadian Institute of Health Research (CIHR) [MOP-130481]
  2. Canada Research Chair in Mechanobiology
  3. Canada Research Chair in Micro and Nanoengineering Systems
  4. NSERC CREATE Program in Microfluidic Applications and Training in Cardiovascular Health (MATCH) scholarship
  5. Heart and Stroke Richard Lewar Centre of Excellence (HSRLCE) studentship

向作者/读者索取更多资源

Native and engineered tissue development are regulated by the integrative effects of multiple micro environmental stimuli. Microfabricated bioreactor array platforms can efficiently dissect cue-response networks, and have recently integrated critical 2D and 3D mechanical stimulation for greater physiological relevance. However, a limitation of these approaches is that assessment of tissue functional properties is typically limited to end-point analyses. Here we report a new deformable membrane platform with integrated strain sensors that enables mechanical stretching or compression of 3D cell-hydrogel arrays and simultaneous measurement of hydrogel construct stiffness in situ. We tested the ability of the integrated strain sensors to measure the evolution of the stiffness of cell-hydrogel constructs for two cases. First, we demonstrated in situ stiffness monitoring of degradable poly (ethylene glycol)-norbornene (PEG-NB) hydrogels embedded with mesenchymal stromal cells (MSCs) and cultured with or without cyclic tensile stimulation for up to 15 days. Whereas statically-cultured hydrogels degraded and softened throughout the culture period, mechanically-stimulated gels initially softened and then recovered their stiffness corresponding to extensive cell network and collagen production. Second, we demonstrated in situ measurement of compressive stiffening of MSC-seeded PEG-NB gels cultured statically under osteogenic conditions, corresponding to increased mineralization and cellularization. This measurement technique can be generalized to other relevant bioreactor and organ-on-a-chip platforms to facilitate online, non-invasive, and high-throughput functional analysis, and to provide insights into the dynamics of engineered tissue development that are otherwise not available. (C) 2018 Elsevier Ltd. All rights reserved.

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