Abstract

The mechanical properties of the extracellular microenvironment, including its stiffness, play a crucial role in stem cell fate determination. Although previous studies have demonstrated that the developing brain exhibits spatiotemporal diversity in stiffness, it remains unclear how stiffness regulates stem cell fate towards specific neural lineages. Here, we established a culture substrate that reproduces the stiffness of brain tissue using tilapia collagen for in vitro reconstitution assays. By adding crosslinkers, we obtained gels that are similar in stiffness to living brain tissue (150–1500 Pa). We further examined the capability of the gels serving as a substrate for stem cell culture and the effect of stiffness on neural lineage differentiation using human iPS cells. Surprisingly, exposure to gels with a stiffness of approximately 1500 Pa during the early period of neural induction promoted the production of dorsal cortical neurons. These findings suggest that brain-stiffness-mimicking gel has the potential to determine the terminal neural subtype. Taken together, the crosslinked tilapia collagen gel is expected to be useful in various reconstitution assays that can be used to explore the role of stiffness in neurogenesis and neural functions. The enhanced production of dorsal cortical neurons may also provide considerable advantages for neural regenerative applications.

Highlights

  • Determination of the fate of pluripotent stem cells and their development into functional cells is one of the crucial issues in the fields of developmental biology and regenerative medicine

  • We previously reported the systematic analysis of living brain tissue stiffness during development[13]

  • These results demonstrate that the tilapia collagen gel established here can be utilized for neural induction from pluripotent cells and that exposure to gels of a particular stiffness during the initial stage of neural induction can determine the direction of differentiation towards a specific neural lineage

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Summary

Introduction

Determination of the fate of pluripotent stem cells and their development into functional cells is one of the crucial issues in the fields of developmental biology and regenerative medicine. Brain tissue showed lower stiffness, ranging from 102 to 103 Pa7–14 Despite these findings, little is known about how tissue stiffness affects the determination of stem cell fate towards specific cellular subtypes either in vitro or in vivo. The neural characteristics acquired after 5 days of neural induction on a gel with a stiffness of 1500 Pa significantly switched to the lineage of dorsal forebrain neurons These results demonstrate that the tilapia collagen gel established here can be utilized for neural induction from pluripotent cells and that exposure to gels of a particular stiffness during the initial stage of neural induction can determine the direction of differentiation towards a specific neural lineage

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