journal article·2016-05-09

Hydrogels with Dual Gradients of Mechanical and Biochemical Cues for Deciphering Cell-Niche Interactions

Xinming Tong, James Jiang, Danqing Zhu, Fan Yang

Publisher page

Abstract

Cell niche is a multifactorial environment containing complex interactions between biochemical and physical cues. Although extensive studies have examined the effects of biochemical or physical cues alone on cell fate, how biochemical and mechanical signals interact to influence cell fates remains largely unknown. To address this challenge, here we report a polyethylene glycol-based gradient hydrogel platform as biomimetic cell niche containing independently tunable matrix stiffness and biochemical ligand density. The versatility of this platform is demonstrated by fabricating and characterizing single gradient or orthogonally aligned dual gradient hydrogels. These gradients result in differential elongation and spreading of human fibroblasts. Both hydrogel stiffness and biochemical ligand density are independently tunable by sequential photopolymerization. By controlling light exposure, a broad range of hydrogel stiffness and different types/doses of biochemical ligands can be incorporated. Such tunability facilitates customization of this platform for investigating complex cell-niche interactions associated with various cell types, such as stem cells and cancer cells. The outcomes of such studies may help identify optimal niche cues to promote desiralbe stem fates and tissue regeneration or inhibit diseases progression.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Cellular Mechanics and Interactions · 3D Printing in Biomedical Research · Silk-based biomaterials and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Bioengineering, Stanford University School of Medicine, 300 Pasteur Drive, Edwards R105, Stanford, California 94305, United States

Funding

National Institute of Dental and Craniofacial Research · California Institute for Regenerative Medicine · Alliance for Cancer Gene Therapy · National Institute of Arthritis and Musculoskeletal and Skin Diseases · Division of Chemical, Bioengineering, Environmental, and Transport Systems · Stanford Chemistry, Engineering and Medicine for Human Health, Stanford University · Child Health Research Institute, Stanford University · James H. Clark Center, Stanford University

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