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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Environmental Sources Nanoplastics Sign in to save

Strong Elastic Protein Nanosheets Enable the Culture and Differentiation of Induced Pluripotent Stem Cells on Microdroplets

2023 4 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Elijah Mojares, Elijah Mojares, Alexandra Chrysanthou, Alexandra Chrysanthou, Alexandra Chrysanthou, Alexandra Chrysanthou, Elijah Mojares, Elijah Mojares, Julien E. Gautrot Julien E. Gautrot Alexandra Chrysanthou, Julien E. Gautrot Julien E. Gautrot Julien E. Gautrot Julien E. Gautrot Alexandra Chrysanthou, Julien E. Gautrot

Summary

Researchers developed elastic protein nanosheets to stabilize liquid-liquid interfaces in microdroplets, enabling the adhesion, expansion, and maintenance of stemness by induced pluripotent stem cells (iPSCs), demonstrating a scalable microfluidic platform for stem cell culture and differentiation.

Study Type In vitro

Abstract Advances in stem cell technologies, revolutionising regenerative therapies and advanced in vitro testing, require novel cell manufacturing pipelines able to cope with scale up and parallelisation. Microdroplet technologies, which have transformed single cell sequencing and other cell-based assays, are attractive in this context, but the inherent soft mechanics of liquid-liquid interfaces is typically thought to be incompatible with the expansion of induced pluripotent stem cells (iPSCs), and their differentiation. In this work, we report the design of protein nanosheets stabilising liquid-liquid interfaces and enabling the adhesion, expansion and retention of stemness by iPSCs. We use microdroplet microfluidic chips to control the formulation of droplets with defined dimensions and size distributions and demonstrate that these sustain high expansion rates, with excellent retention of stem cell marker expression. We further demonstrate that iPSCs cultured in such conditions retain the capacity to differentiate into cardiomyocytes and demonstrate such process on droplets. This work provides clear evidence that local nanoscale mechanics, associated with interfacial viscoelasticity, provides strong cues able to regulate and maintain pluripotency, as well as to support commitment in defined differentiation conditions. Microdroplet technologies appear as attractive candidates to transform cell manufacturing pipelines, bypassing significant hurdles paused by solid substrates and microcarriers.

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