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协调干细胞对翻译支架反应的分子机制。

Molecular mechanisms orchestrating the stem cell response to translational scaffolds.

作者信息

Ozdemir Tugba, Higgins Andrew M, Brown Justin L

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2015 Aug;2015:1749-52. doi: 10.1109/EMBC.2015.7318716.

Abstract

A 2013 Perspective in Science titled "Deconstructing Dimensionality" noted the importance of fiber morphology on cell phenotype, concluding with the statement "Identifying the mechanisms by which cells assess the nature of their environment will advance basic cell biology and facilitate the development of synthetic matrices for specific tissue engineering applications." Nanofibers have revolutionized scaffold-based approaches for musculoskeletal tissues; demonstrating surprising efficacy over promoting mesenchymal stem cell, MSC, differentiation down multiple musculoskeletal lineages. Understanding the fundamental mechanisms involved will allow the future design of nanofiber-based scaffolds to target a lineage with specificity. This article focuses on how three geometry sensors: focal adhesions, membrane associated vesicle stabilizing and trafficking proteins, and adherens junctions; potentially regulate MSC lineage commitment in response to bio-instructive nanofibers.

摘要

2013年发表在《科学展望》上一篇题为《解构维度》的文章指出了纤维形态对细胞表型的重要性,文章结尾指出:“确定细胞评估其周围环境性质的机制将推动基础细胞生物学的发展,并促进用于特定组织工程应用的合成基质的开发。”纳米纤维彻底改变了用于肌肉骨骼组织的基于支架的方法;在促进间充质干细胞(MSC)向多个肌肉骨骼谱系分化方面显示出惊人的功效。了解其中的基本机制将有助于未来设计基于纳米纤维的支架,以特异性地靶向某一谱系。本文重点探讨三种几何传感器:粘着斑、膜相关囊泡稳定和运输蛋白以及紧密连接;如何潜在地调节MSC谱系定向,以响应具有生物指导作用的纳米纤维。

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