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微图案化 PLGA 纳米纤维坑中唾液腺细胞的分化和组织。

Salivary gland cell differentiation and organization on micropatterned PLGA nanofiber craters.

机构信息

College of Nanoscale Science and Engineering, University at Albany, State University of New York, 257 Fuller Road, Albany, NY 12203, USA.

出版信息

Biomaterials. 2013 Sep;34(28):6773-84. doi: 10.1016/j.biomaterials.2013.05.061. Epub 2013 Jun 15.

Abstract

There is a need for an artificial salivary gland as a long-term remedy for patients suffering from salivary hypofunction, a leading cause of chronic xerostomia (dry mouth). Current salivary gland tissue engineering approaches are limited in that they either lack sufficient physical cues and surface area needed to facilitate epithelial cell differentiation, or they fail to provide a mechanism for assembling an interconnected branched network of cells. We have developed highly-ordered arrays of curved hemispherical "craters" in polydimethylsiloxane (PDMS) using wafer-level integrated circuit (IC) fabrication processes, and lined them with electrospun poly-lactic-co-glycolic acid (PLGA) nanofibers, designed to mimic the three-dimensional (3-D) in vivo architecture of the basement membrane surrounding spherical acini of salivary gland epithelial cells. These micropatterned scaffolds provide a method for engineering increased surface area and were additionally investigated for their ability to promote cell polarization. Two immortalized salivary gland cell lines (SIMS, ductal and Par-C10, acinar) were cultured on fibrous crater arrays of various radii and compared with those grown on flat PLGA nanofiber substrates, and in 3-D Matrigel. It was found that by increasing crater curvature, the average height of the cell monolayer of SIMS cells and to a lesser extent, Par-C10 cells, increased to a maximum similar to that seen in cells grown in 3-D Matrigel. Increasing curvature resulted in higher expression levels of tight junction protein occludin in both cell lines, but did not induce a change in expression of adherens junction protein E-cadherin. Additionally, increasing curvature promoted polarity of both cell lines, as a greater apical localization of occludin was seen in cells on substrates of higher curvature. Lastly, substrate curvature increased expression of the water channel protein aquaporin-5 (Aqp-5) in Par-C10 cells, suggesting that curved nanofiber substrates are more suitable for promoting differentiation of salivary gland cells.

摘要

需要有一种人工唾液腺作为治疗唾液功能低下症(慢性口干症的主要病因)患者的长期疗法。目前的唾液腺组织工程方法存在局限性,因为它们要么缺乏促进上皮细胞分化所需的足够物理线索和表面积,要么无法提供组装细胞相互连接的分支网络的机制。我们使用晶圆级集成电路 (IC) 制造工艺在聚二甲基硅氧烷 (PDMS) 中开发了高度有序的弯曲半球形“火山口”阵列,并在其表面排列了电纺聚乳酸-共-羟基乙酸 (PLGA) 纳米纤维,旨在模仿唾液腺上皮细胞的球形腺泡周围的三维 (3-D) 体内基底膜结构。这些微图案化支架提供了一种增加表面积的方法,并进一步研究了它们促进细胞极化的能力。两种永生化唾液腺细胞系 (SIMS,导管和 Par-C10,腺泡) 在具有不同半径的纤维火山口阵列上培养,并与在平板 PLGA 纳米纤维基底上以及在 3-D Matrigel 中培养的细胞进行了比较。结果发现,通过增加火山口曲率,SIMS 细胞和在较小程度上 Par-C10 细胞的单层细胞的平均高度增加到类似于在 3-D Matrigel 中培养的细胞的最大值。曲率增加导致两种细胞系中紧密连接蛋白 Occludin 的表达水平升高,但不会诱导黏着连接蛋白 E-cadherin 的表达变化。此外,曲率增加促进了两种细胞系的极性,因为在曲率较高的基底上,Occludin 的顶端定位更多。最后,基底曲率增加了 Par-C10 细胞中水通道蛋白 Aqp-5 的表达,表明弯曲纳米纤维基底更适合促进唾液腺细胞的分化。

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