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首页> 外文期刊>Biomaterials Science >In vitro model alveoli from photodegradable microsphere templates
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In vitro model alveoli from photodegradable microsphere templates

机译:可光降解微球模板的体外模型肺泡

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摘要

Recreating the 3D cyst-like architecture of the alveolar epithelium in vitro has been challenging to achieve in a controlled fashion with primary lung epithelial cells. Here, we demonstrate model alveoli formed within a tunable synthetic biomaterial platform using photodegradable microspheres as templates to create physiologically relevant, cyst structures. Poly(ethylene glycol) (PEG)-based hydrogels were polymerized in suspension to form microspheres on the order of 120 mu m in diameter. The gel chemistry was designed to allow erosion of the microspheres with cytocompatible light doses (<= 15 min exposure to 10 mW cm(-2) of 365 nm light) via cleavage of a photolabile nitrobenzyl ether crosslinker. Epithelial cells were incubated with intact microspheres, modified with adhesive peptide sequences to facilitate cellular attachment to and proliferation on the surface. A tumor-derived alveolar epithelial cell line, A549, completely covered the microspheres after only 24 hours, whereas primary mouse alveolar epithelial type II (ATII) cells took similar to 3 days. The cell-laden microsphere structures were embedded within a second hydrogel formulation at user defined densities; the microsphere templates were subsequently removed with light to render hollow epithelial cysts that were cultured for an additional 6 days. The resulting primary cysts stained positive for cell-cell junction proteins (beta-catenin and ZO-1), indicating the formation of a functional epithelial layer. Typically, primary ATII cells differentiated in culture to the alveolar epithelial type I (ATI) phenotype; however, each cyst contained similar to 1-5 cells that stained positive for an ATII marker (surfactant protein C), which is consistent with ATII cell numbers in native mouse alveoli. This biomaterial-templated alveoli culture system should be useful for future experiments to study lung development and disease progression, and is ideally suited for co-culture experiments where pulmonary fibroblasts or endothelial cells could be presented in the hydrogel surrounding the epithelial cysts.
机译:体外重建肺泡上皮的3D囊样结构对于以原代肺上皮细胞以可控方式实现具有挑战性。在这里,我们演示了使用可光降解微球作为模板在可调节的合成生物材料平台内形成的模型肺泡,以创建生理相关的囊肿结构。使基于聚(乙二醇)(PEG)的水凝胶在悬浮液中聚合以形成直径为120μm量级的微球。凝胶化学设计为通过裂解光不稳定的硝基苄基醚交联剂,使具有细胞相容性光剂量(<= 15分钟,暴露于10 mW cm(-2)的365 nm光中)腐蚀微球。上皮细胞与完整的微球孵育,并用粘附肽序列修饰,以促进细胞附着在表面并在表面增殖。肿瘤来源的肺泡上皮细胞系A549仅在24小时后就完全覆盖了微球,而原代小鼠肺泡上皮II型(ATII)细胞则耗时约3天。载有细胞的微球结构以用户定义的密度嵌入第二种水凝胶制剂中。随后用光除去微球模板以产生空心上皮囊肿,将其培养另外6天。所得的原发性囊肿对细胞-细胞连接蛋白(β-catenin和ZO-1)染色呈阳性,表明形成了功能性上皮层。通常,原代ATII细胞在培养中分化为肺泡上皮I型(ATI)表型。但是,每个囊肿都含有类似于1-5个细胞的ATII标记(表面活性蛋白C)染色阳性,这与天然小鼠肺泡中的ATII细胞数一致。这种以生物材料为模板的肺泡培养系统应可用于未来的实验来研究肺部发育和疾病进展,并且非常适合于共培养实验,在该实验中,肺成纤维细胞或内皮细胞可以出现在上皮囊肿周围的水凝胶中。

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