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连续光微影生成微盘阵列之均一细胞外基质涂布制作与生物评估。

Fabrication and biological evaluation of uniform extracellular matrix coatings on discontinuous photolithography generated micropallet arrays.

机构信息

Department of Biomedical Engineering, School of Engineering, University of California at Irvine, Irvine, California 92697, USA.

出版信息

J Biomed Mater Res A. 2010 Nov;95(2):401-12. doi: 10.1002/jbm.a.32854.

Abstract

The recent identification of rare cell populations within tissues that are associated with specific biological behaviors, for example, progenitor cells, has illuminated a limitation of current technologies to study such adherent cells directly from primary tissues. The micropallet array is a recently developed technology designed to address this limitation by virtue of its capacity to isolate and recover single adherent cells on individual micropallets. The capacity to apply this technology to primary tissues and cells with restricted growth characteristics, particularly adhesion requirements, is critically dependent on the capacity to generate functional extracellular matrix (ECM) coatings. The discontinuous nature of the micropallet array surface provides specific constraints on the processes for generating the desired ECM coatings that are necessary to achieve the full functional capacity of the micropallet array. We have developed strategies, reported herein, to generate functional coatings with various ECM protein components: fibronectin, EHS tumor basement membrane extract, collagen, and laminin-5; confirmed by evaluation for rapid cellular adherence of four dissimilar cell types: fibroblast, breast epithelial, pancreatic epithelial, and myeloma. These findings are important for the dissemination and expanded use of micropallet arrays and similar microtechnologies requiring the integrated use of ECM protein coatings to promote cellular adherence.

摘要

最近在与特定生物学行为相关的组织中鉴定出了稀有细胞群体,例如祖细胞,这凸显了当前技术的一个局限性,即无法直接从原发性组织中研究这些贴壁细胞。微珠阵列是一种最近开发的技术,其设计目的是通过其在单个微珠上分离和回收单个贴壁细胞的能力来克服这一局限性。将该技术应用于具有受限生长特性(尤其是粘附要求)的原发性组织和细胞的能力,严重依赖于生成功能性细胞外基质 (ECM) 涂层的能力。微珠阵列表面的不连续性对生成所需 ECM 涂层的过程提出了具体的限制,这些涂层是实现微珠阵列全部功能的必要条件。我们已经开发了一些策略,本文对此进行了报道,以生成具有各种 ECM 蛋白成分的功能性涂层:纤连蛋白、EHS 肿瘤基底膜提取物、胶原蛋白和层粘连蛋白-5;通过评估四种不同细胞类型(成纤维细胞、乳腺上皮细胞、胰腺上皮细胞和骨髓瘤细胞)的快速细胞黏附来证实。这些发现对于微珠阵列和类似的微技术的传播和广泛应用非常重要,这些技术需要整合使用 ECM 蛋白涂层来促进细胞黏附。

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