4.8 Review

Biomaterials in co-culture systems: Towards optimizing tissue integration and cell signaling within scaffolds

Journal

BIOMATERIALS
Volume 35, Issue 15, Pages 4465-4476

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.02.023

Keywords

Co-culture; Biomaterials; Tissue engineering; Cellular interactions; Stem cells; Monocytes

Funding

  1. Natural Sciences and Engineering Research Council (NSERC) [360520]
  2. NSERC Alexander Graham Bell Canada Graduate Scholarship [CGS D3]
  3. Canadian Institutes of Health Research (CIHR) [230762]
  4. Ontario Graduate Scholarship Program
  5. CIHR-Cell Signals Training Fellowship program [TGF-53877]

Ask authors/readers for more resources

Most natural tissues consist of multi-cellular systems made up of two or more cell types. However, some of these tissues may not regenerate themselves following tissue injury or disease without some form of intervention, such as from the use of tissue engineered constructs. Recent studies have increasingly used co-cultures in tissue engineering applications as these systems better model the natural tissues, both physically and biologically. This review aims to identify the challenges of using co-culture systems and to highlight different approaches with respect to the use of biomaterials in the use of such systems. The application of co-culture systems to stimulate a desired biological response and examples of studies within particular tissue engineering disciplines are summarized. A description of different analytical co-culture systems is also discussed and the role of biomaterials in the future of co-culture research are elaborated on. Understanding the complex cell cell and cell biomaterial interactions involved in co-culture systems will ultimately lead the field towards biomaterial concepts and designs with specific biochemical, electrical, and mechanical characteristics that are tailored towards the needs of distinct co-culture systems. (C) 2014 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
Article Engineering, Biomedical

A novel capsid-XL32-derived adeno-associated virus serotype prompts retinal tropism and ameliorates choroidal neovascularization

Lin-Lin Luo, Jie Xu, Bing-Qiao Wang, Chen Chen, Xi Chen, Qiu-Mei Hu, Yu-Qiu Wang, Wan-Yun Zhang, Wan-Xiang Jiang, Xin-Ting Li, Hu Zhou, Xiao Xiao, Kai Zhao, Sen Lin

Summary: A novel AAV serotype, AAVYC5, introduced in this study, showed more efficient transduction into multiple retinal layers compared to AAV2, and enabled successful delivery of anti-angiogenic molecules in mice and non-human primates.

BIOMATERIALS (2024)