Abstract

This article presents data related to the research article “Systematic optimization of an engineered hydrogel allows for selective control of human neural stem cell survival and differentiation after transplantation in the stroke brain” (P. Moshayedi, L.R. Nih, I.L. Llorente, A.R. Berg, J. Cinkornpumin, W.E. Lowry et al., 2016) [1] and focuses on the biocompatibility aspects of the hydrogel, including its stiffness and the inflammatory response of the transplanted organ. We have developed an injectable hyaluronic acid (HA)-based hydrogel for stem cell culture and transplantation, to promote brain tissue repair after stroke. This 3D biomaterial was engineered to bind bioactive signals such as adhesive motifs, as well as releasing growth factors while supporting cell growth and tissue infiltration. We used a Design of Experiment approach to create a complex matrix environment in vitro by keeping the hydrogel platform and cell type constant across conditions while systematically varying peptide motifs and growth factors. The optimized HA hydrogel promoted survival of encapsulated human induced pluripotent stem cell derived-neural progenitor cells (iPS-NPCs) after transplantation into the stroke cavity and differentially tuned transplanted cell fate through the promotion of glial, neuronal or immature/progenitor states. The highlights of this article include: (1) Data of cell and bioactive signals addition on the hydrogel mechanical properties and growth factor diffusion, (2) the use of a design of Experiment (DOE) approach (M.W. 2 Weible and T. Chan-Ling, 2007) [2] to select multi-factorial experimental conditions, and (3) Inflammatory response and cell survival after transplantation.

Highlights

  • Engineered HA hydrogel for stem cell transplantation in the brain: Biocompatibility data using a design of experiment approach

  • We have developed an injectable hyaluronic acid (HA)-based hydrogel for stem cell culture and transplantation, to promote brain tissue repair after stroke

  • Biology, Engineering, Material Sciences Biomaterial, Stem cell transplantation, brain repair Graph, figure, table Rheology, Elisa, Microscopy Analyzed Cell encapsulation in hydrogel before transplantation Human neural progenitor cell, 3D culture and brain transplantation Los Angeles, California, USA Data is provided in the article

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Summary

Cell culture

Induced pluripotent stem cells (iPS) were obtained from human fibroblasts [6] and directly differentiated in 2D culture from iPS through formation of neural rosettes [7]. On the day of transplantation, human iPS-NPCs were harvested by a 5 min incubation in presence of TrypLE (Life Technologies), centrifuged at 300 g for 5 min, re-suspended in animal origin-free culture medium and kept on ice before injection

Hyaluronic acid modification
Heparin modification
Gelation
Cell survival in vitro
Design of experiments
Inducing stroke and transplantation
2.10. Tissue processing
Findings
2.12. Statistics
Full Text
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