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Transient Changes in Stem Cells Induced by Electrical Stimulation - Session Mechanobiology
Dr. Amy GelmiDone
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Pick and Place of Neuronal Cells and Spheroids using FluidFM for the Construction of Neuronal Networks - Session Mechanobiology
Dr. Sinead ConnollyDone
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Quantification of micro/nano objects movement under vortex force by Fluidic Force Microscopy - Session Mechanobiology
Dr. Yonghui ZhangDone
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Keynote Speaker - Robotic FluidFM in the Nanobiosensorics Lab: from large-area printing to high-throughput adhesion and injection of single cells - Session Mechanobiology
Dr. Robert HorvathDone
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Keynote Speaker: Evaluation of FluidFM technology for single-cell genome editing - Session - Genome Engineering
Dr. Simona PatangeDone
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Coffee Break
Done
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Single-cell Nanobiopsy Enables Multigenerational Longitudinal Transcriptomics of Cancer Cells - Session Live-seq & Biopsies
Dr. Fabio MarcuccioDone
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Engineering Endosymbiotic Growth of E. coli in Mammalian Cells - Session Genome Engineering
Chantal ErnstDone
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Characterization of Mechanotransduction-induced changes in cell identity of PDAC in response to Nanotopography - Session Live-seq & Biopsies
Pr. Dr. Carmelo FerraiDone
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Registration & Coffee Break
Done
Abstract
Utilizing Atomic Force Microscopy (AFM), we have investigated the distinct single-cell characteristics of induced pluripotent stem cells (iPSCs) and their cardiomyocyte derivatives (iPSC-CMs). Our study reveals significant shifts in cell elasticity and mass during differentiation and maturation, indicating AFM's potential as a reliable tool to track the progression of iPSC-CMs. Originating from mature cells like human skin cells, iPSCs can differentiate into various cell types, with iPSC-CMs holding promise for applications in cell therapy, drug testing, and cardiac disease research. Increasingly acknowledged for their role in drug evaluation, iPSC-CMs are advancing the field of personalized medicine, and their potential for heart tissue repair underscores their importance in regenerative medicine. The success of these applications hinges on accurately characterizing the cells at the single-cell level, specifically their maturation status. We, for the first time, successfully used AFM to discern between stages of cell differentiation and maturation based on changes in cell elasticity and mass. The integration of AFM with techniques for isolating cells and extracting genomic content can further deepen our understanding of iPSC differentiation, underscoring the expansive potential of AFM as a comprehensive tool for single-cell analysis.
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