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用于干细胞调控的纳米级沟槽和脊状形貌的仿生动力学

Biomimetic Dynamics of Nanoscale Groove and Ridge Topography for Stem Cell Regulation.

作者信息

Hong Hyunsik, Kim Dahee, Jung Hwapyung, Kim Seongyeol, Min Sunhong, Kim Chowon, Kim Kanghyeon, Rha Hyunji, Kang Heemin

机构信息

Department of Materials Science and Engineering, Korea University, Seoul, 02841, Republic of Korea.

College of Medicine, Korea University, Seoul, 02841, Republic of Korea.

出版信息

Adv Mater. 2025 Jul;37(30):e2419416. doi: 10.1002/adma.202419416. Epub 2025 Apr 26.

Abstract

Native extracellular matrix exhibits multiscale groove and ridge structures that continuously change, such as collagen fibril-based nanogrooves in bone tissue, and regulate cellular responses. However, dynamic switching between groove and ridge nanostructures at the molecular level has not been demonstrated. Herein, materials capable of dynamic groove-ridge switching at tens-of-nanometers scale are developed by flexibly conjugating RGD-magnetically activatable nanoridges (MANs) to non-magnetic nanogrooves with independently tuned widths comparable to the sizes of integrin-presenting filopodia by modulating hydrophobicity in bicontinuous microemulsion, allowing for cyclic modulation of RGD accessibility and cellular adhesion. Nanogrooves with medium width restrict RGD accessibility in the "groove" state in which the RGD-MANs are buried, which is reversed by magnetically raising them to protrude and form the "ridge" state that fully exposes the RGDs. This reversibly stimulates integrin recruitment, focal adhesion complex assembly, mechanotransduction, and differentiation of stem cells in vivo. This is the first demonstration of molecular-level groove and ridge nanostructures that exhibit unprecedented switchability between groove and ridge nanostructures. Versatile tuning of the width, height, pitch, and shape of intricate nanogroove structures with remote manipulability can enlighten the understanding of molecular-scale cell-ligand interactions for stem cell engineering-based treatment of aging, injuries, and stress-related diseases.

摘要

天然细胞外基质呈现出不断变化的多尺度沟槽和脊状结构,例如骨组织中基于胶原纤维的纳米沟槽,并调节细胞反应。然而,在分子水平上沟槽和脊状纳米结构之间的动态切换尚未得到证实。在此,通过在双连续微乳液中调节疏水性,将RGD磁性可激活纳米脊(MANs)灵活地连接到宽度与呈现整合素的丝状伪足大小相当的非磁性纳米沟槽上,开发出了能够在几十纳米尺度上进行动态沟槽-脊切换的材料,从而实现RGD可及性和细胞粘附的循环调节。中等宽度的纳米沟槽在RGD-MANs被掩埋的“沟槽”状态下限制RGD可及性,通过磁性作用使其凸起形成完全暴露RGD的“脊”状态可逆转这种情况。这在体内可逆地刺激整合素募集、粘着斑复合物组装、机械转导和干细胞分化。这是首次证明分子水平的沟槽和脊状纳米结构在沟槽和脊状纳米结构之间表现出前所未有的可切换性。对具有远程可操纵性的复杂纳米沟槽结构的宽度、高度、间距和形状进行通用调节,有助于深入理解基于干细胞工程治疗衰老、损伤和应激相关疾病的分子尺度细胞-配体相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e8b/12306399/120a5d54f77d/ADMA-37-2419416-g004.jpg

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