The Rapid Generation of Cell-Laden, FACS-Compatible Collagen Gels

Author:

Xiao Yi123,Huang Qiaoling4,Collins Jesse W.1ORCID,Brouchon Julie1,Nelson Jeffery A.5,Niziolek Zachary1,O’Neil Alison6ORCID,Ye Fangfu37,Weitz David A.1,Heyman John A.1ORCID

Affiliation:

1. Experimental Soft Condensed Matter Group, School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA

2. Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Department of Pharmacy, School of Medicine, Hunan Normal University, Changsha 410013, China

3. Oujiang Laboratory (Zhejiang Laboratory for Regenerative Medicine, Vision and Brain Health), Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou 325000, China

4. Department of Physics, Xiamen University, Xiamen 361005, China

5. Faculty of Arts and Sciences, Bauer Flow Cytometry Core, Harvard University, Cambridge, MA 02138, USA

6. Department of Chemistry, Wesleyan University, Middletown, CT 06459, USA

7. Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China

Abstract

A three-dimensional cell culture in hydrogel beads can support cell growth and differentiation into multi-cellular structures, and these gel beads could be used as building blocks for more complex three-dimensional assemblies. This requires hydrogel beads that are robust enough to sort via FACS yet can be degraded by cell-secreted enzymes. Collagen polymers form hydrogels that are excellent cell growth substrates; however, collagen-containing hydrogel beads typically include additional polymers that limit their degradation. Here, we introduce a simple microfluidic method to generate robust, sortable, cell-laden collagen hydrogel beads. We use on-device pH control to trigger collagen gelation without exposing cells to low pH, ensuring high cell viability. We fabricate microfluidic devices to generate droplets with a wide size range, as demonstrated by production of both small (~55 µm diameter) and large (~300 µm diameter) collagen gels. All hydrogels are sufficiently robust to allow for sorting using FACS. Moreover, high cell viability is maintained throughout the process.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Harvard University

Higher Education Discipline Innovation Project

Massachusetts Life Sciences Center Award

The Foundation for Aids Research

Ragon Institute

Health@InnoHK program of the Innovation and Technology Commission of the Hong Kong SAR Government

National Key Research and Development Program of China

Publisher

MDPI AG

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