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Peptide Electrostatic Modulation Directs Human Neural Cell Fate
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DOI：10.1002/advs.202507946.png)
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Abstract
En 中文
Supramolecular self-assembled systems have emerged as versatile platforms for engineering biomimetic environments that precisely regulate cellular behavior. These materials have tunable properties such as stiffness, hydrophobicity, and molecular composition, allowing for customization of their structure and function. Despite significant advances, the specific role of electrostatic properties in modulating cellular responses within supramolecular assemblies remains poorly understood. Here, a peptide library with diverse electrostatic profiles is designed to systematically investigate their influence on the bioactivity of supramolecular assemblies for neural regeneration. Combining computational and experimental methods, the self-assembly conditions of these peptides are optimized to create stable, biologically relevant architectures. Using human neural progenitor cell (hNPC) cultures, it is demonstrated that negatively charged environments enhance cell survival and promote neuronal differentiation. Specifically, high negative charges activate critical signaling pathways, including the mitogen-activated protein kinase (MAPK) cascade and cell adhesion mechanisms, leading to neuronal lineage commitment. This study establishes a novel framework for the design of supramolecular systems, offering an unprecedented ability to analyze specific parameters in cell behavior. By achieving control beyond conventional biomaterials, this work provides valuable insights into the complex interplay of biophysical and biochemical cues in the native neural microenvironment, with implications for regenerative medicine and biomaterial design.
Keywords:
charge screening
human neural progenitor cells
membrane
molecular dynamics
proteomics
self-assemblies
supramolecular structures
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