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用于调节上皮形态发生的生物粘附水凝胶微环境。

Bioadhesive hydrogel microenvironments to modulate epithelial morphogenesis.

作者信息

Chung I-Ming, Enemchukwu Nduka O, Khaja Sirajud D, Murthy Niren, Mantalaris Athanasios, García Andrés J

机构信息

Biological Systems Engineering Laboratory, Department of Chemical Engineering, Imperial College London, South Kensington campus, London SW7 2AZ, United Kingdom.

出版信息

Biomaterials. 2008 Jun;29(17):2637-45. doi: 10.1016/j.biomaterials.2008.03.008.


DOI:10.1016/j.biomaterials.2008.03.008
PMID:18377982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2408686/
Abstract

Epithelial cells polarize and differentiate into organotypic cell aggregates in response to cell-cell and cell-matrix interactions. For example, Madin-Darby Canine Kidney (MDCK) cells form spherical cell aggregates (cysts) with distinct apical and basolateral polarity when cultured three dimensionally (embedded) in type I collagen gels. To investigate the effects of individual extracellular factors on epithelial morphogenesis, we engineered fast degrading protease-responsive polyethylene glycol (PEG) hydrogels functionalized with controlled densities of various bioligands (RGD peptide, laminin-1 (LN)) to allow 3D culturing of MDCK cells, cyst expansion, and morphogenesis/polarization. Cysts formed after 15 days of culture in these hydrogels were analyzed with multiphoton fluorescence microscopy for markers of apical and basolateral membrane domains. Epithelial cysts formed in bioadhesive ligand-functionalized PEG gels exhibited a higher frequency of central lumen and interior apical pole formation as well as basolateral polarization compared to those of unmodified PEG hydrogels. These results demonstrate that incorporation of specific bioadhesive motifs into synthetic hydrogels provides 3D culture environments that support epithelial morphogenesis. These microenvironments provide a flexible and controlled system for systematic investigations into normal and pathologic morphogenic behaviours as well as synthetic environments for promoting tissue morphogenesis for regenerative medicine applications.

摘要

上皮细胞会响应细胞间和细胞与基质间的相互作用而极化并分化为器官型细胞聚集体。例如,当在I型胶原凝胶中进行三维(包埋)培养时,马-达犬肾(MDCK)细胞会形成具有明显顶端和基底外侧极性的球形细胞聚集体(囊肿)。为了研究单个细胞外因子对上皮形态发生的影响,我们设计了快速降解的蛋白酶响应性聚乙二醇(PEG)水凝胶,这些水凝胶用各种生物配体(RGD肽、层粘连蛋白-1(LN))的可控密度进行功能化修饰,以实现MDCK细胞的三维培养、囊肿扩张以及形态发生/极化。在这些水凝胶中培养15天后形成的囊肿,通过多光子荧光显微镜分析顶端和基底外侧膜结构域的标志物。与未修饰的PEG水凝胶相比,在生物粘附配体功能化的PEG凝胶中形成的上皮囊肿表现出更高频率的中央管腔和内部顶端极形成以及基底外侧极化。这些结果表明,将特定的生物粘附基序纳入合成水凝胶可提供支持上皮形态发生的三维培养环境。这些微环境为系统研究正常和病理形态发生行为提供了一个灵活且可控的系统,同时也为再生医学应用中促进组织形态发生提供了合成环境。

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[2]
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[3]
Matrix Degradability Contributes to the Development of Salivary Gland Progenitor Cells with Secretory Functions.

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[5]
Exploiting Meltable Protein Hydrogels to Encapsulate and Culture Cells in 3D.

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[6]
Synthetic Collagen-like Polymer That Undergoes a Sol-Gel Transition Triggered by Acyl Migration at Physiological pH.

Int J Mol Sci. 2022-1-29

[7]
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[9]
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[10]
Effect of incorporating clustered silica nanoparticles on the performance and biocompatibility of catechol-containing PEG-based bioadhesive.

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本文引用的文献

[1]
Modeling dynamic reciprocity: engineering three-dimensional culture models of breast architecture, function, and neoplastic transformation.

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[2]
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Mol Biol Cell. 2005-2

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Nat Cell Biol. 2001-9

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